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primary human bone marrow-derived mscs (bm-msc) pt-2501  (Lonza)


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    Structured Review

    Lonza primary human bone marrow-derived mscs (bm-msc) pt-2501
    Effect of different donor-derived human peripheral blood mononuclear cells (PBMCs) on the in vitro immunomodulatory response of bone marrow (BM)- mesenchymal stem cells <t>(MSCs).</t> (a) Schematic of the protocol for lymphocyte proliferation assays with mitogen as an immunomodulatory potency assay for MSCs. (b) Proliferation of 10 donor-derived PBMCs upon phytohemagglutinin (PHA; 0.2, 0.5, and 1.0 μg/mL) stimulation was assessed through BrdU uptake. BrdU uptake was indicated by luminescence signal (counts per second, CPS). Two-way ANOVA showed that PBMCs proliferation was significantly affected by the stimulating PHA concentration, the presence or absence of MSCs, and their interaction (p < 0.0001). All values indicate the mean ± standard deviation of mean of three biological replicates (n = 3) (∗P < 0.05, ∗∗P < 0.01, ∗∗∗∗P < 0.0001, two-way analysis of variance, followed by Bonferroni's multiple comparison test). (c) Effect of PBMCs derived from 10 donors on the in vitro immunomodulatory response of BM-MSCs. The rate of suppression by BM-MSCs on PBMC proliferation stimulated with three PHA concentrations (0.2, 0.5, and 1.0 μg/mL) is shown as the immunosuppression rate; CPS(PBMC + MSC)/CPS(PBMC).
    Primary Human Bone Marrow Derived Mscs (Bm Msc) Pt 2501, supplied by Lonza, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/primary+human+bone+marrow-derived+mscs/human+mscs/pmc11773150-34-4-9
    Average 90 stars, based on 1 article reviews
    primary human bone marrow-derived mscs (bm-msc) pt-2501 - by Bioz Stars, 2026-11
    90/100 stars

    Images

    1) Product Images from "Increasing robustness of in vitro assay for immnosuppressive effect of mesenchymal stromal/stem cells: The role of inflammatory cytokine production by peripheral blood mononuclear cells"

    Article Title: Increasing robustness of in vitro assay for immnosuppressive effect of mesenchymal stromal/stem cells: The role of inflammatory cytokine production by peripheral blood mononuclear cells

    Journal: Regenerative Therapy

    doi: 10.1016/j.reth.2024.12.016

    Effect of different donor-derived human peripheral blood mononuclear cells (PBMCs) on the in vitro immunomodulatory response of bone marrow (BM)- mesenchymal stem cells (MSCs). (a) Schematic of the protocol for lymphocyte proliferation assays with mitogen as an immunomodulatory potency assay for MSCs. (b) Proliferation of 10 donor-derived PBMCs upon phytohemagglutinin (PHA; 0.2, 0.5, and 1.0 μg/mL) stimulation was assessed through BrdU uptake. BrdU uptake was indicated by luminescence signal (counts per second, CPS). Two-way ANOVA showed that PBMCs proliferation was significantly affected by the stimulating PHA concentration, the presence or absence of MSCs, and their interaction (p < 0.0001). All values indicate the mean ± standard deviation of mean of three biological replicates (n = 3) (∗P < 0.05, ∗∗P < 0.01, ∗∗∗∗P < 0.0001, two-way analysis of variance, followed by Bonferroni's multiple comparison test). (c) Effect of PBMCs derived from 10 donors on the in vitro immunomodulatory response of BM-MSCs. The rate of suppression by BM-MSCs on PBMC proliferation stimulated with three PHA concentrations (0.2, 0.5, and 1.0 μg/mL) is shown as the immunosuppression rate; CPS(PBMC + MSC)/CPS(PBMC).
    Figure Legend Snippet: Effect of different donor-derived human peripheral blood mononuclear cells (PBMCs) on the in vitro immunomodulatory response of bone marrow (BM)- mesenchymal stem cells (MSCs). (a) Schematic of the protocol for lymphocyte proliferation assays with mitogen as an immunomodulatory potency assay for MSCs. (b) Proliferation of 10 donor-derived PBMCs upon phytohemagglutinin (PHA; 0.2, 0.5, and 1.0 μg/mL) stimulation was assessed through BrdU uptake. BrdU uptake was indicated by luminescence signal (counts per second, CPS). Two-way ANOVA showed that PBMCs proliferation was significantly affected by the stimulating PHA concentration, the presence or absence of MSCs, and their interaction (p < 0.0001). All values indicate the mean ± standard deviation of mean of three biological replicates (n = 3) (∗P < 0.05, ∗∗P < 0.01, ∗∗∗∗P < 0.0001, two-way analysis of variance, followed by Bonferroni's multiple comparison test). (c) Effect of PBMCs derived from 10 donors on the in vitro immunomodulatory response of BM-MSCs. The rate of suppression by BM-MSCs on PBMC proliferation stimulated with three PHA concentrations (0.2, 0.5, and 1.0 μg/mL) is shown as the immunosuppression rate; CPS(PBMC + MSC)/CPS(PBMC).

    Techniques Used: Derivative Assay, In Vitro, Potency Assay, Concentration Assay, Standard Deviation, Comparison

    Relationship between the production of cytokines by PHA-stimulated PBMCs and the suppression rate of PBMC proliferation by MSCs in the immunomodulatory potency assay. Spearman correlation analysis between the concentration of each cytokine in the culture supernatant when PBMCs were stimulated with 1.0 μg/mL PHA and the rate of proliferation inhibition by BM-MSCs in the immunomodulatory potency assay is shown with linear regression lines and their 95 % confidential intervals. r, correlation coefficient.
    Figure Legend Snippet: Relationship between the production of cytokines by PHA-stimulated PBMCs and the suppression rate of PBMC proliferation by MSCs in the immunomodulatory potency assay. Spearman correlation analysis between the concentration of each cytokine in the culture supernatant when PBMCs were stimulated with 1.0 μg/mL PHA and the rate of proliferation inhibition by BM-MSCs in the immunomodulatory potency assay is shown with linear regression lines and their 95 % confidential intervals. r, correlation coefficient.

    Techniques Used: Potency Assay, Concentration Assay, Inhibition

    Inter-test variability in the rate of proliferation inhibition of PBMCs by repeated one-way MLR assay.
    Figure Legend Snippet: Inter-test variability in the rate of proliferation inhibition of PBMCs by repeated one-way MLR assay.

    Techniques Used: Inhibition, Mlr Assay

    Figure summarizing the flow of the reversed effects of MSCs depending on the cytokine production concentration of PHA-stimulated PBMCs in the immunomodulatory potency assay. The illustration of MSC in the figure was done using BioRender: scientific image and illustration software.
    Figure Legend Snippet: Figure summarizing the flow of the reversed effects of MSCs depending on the cytokine production concentration of PHA-stimulated PBMCs in the immunomodulatory potency assay. The illustration of MSC in the figure was done using BioRender: scientific image and illustration software.

    Techniques Used: Concentration Assay, Potency Assay, Software

    Related Articles

    Concentration Assay:

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    MTT Assay:

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    CCK-8 Assay:

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    Cell Counting:

    Article Title: Effects of organophosphates on the regulation of mesenchymal stem cell proliferation and differentiation.
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    Article Title: The Effects of ROCK Inhibition on Mesenchymal Stem Cell Chondrogenesis Are Culture Model Dependent
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    Article Title: The Effects of ROCK Inhibition on Mesenchymal Stem Cell Chondrogenesis Are Culture Model Dependent
    Article Snippet: Primary human bone marrow-derived MSCs were purchased from a commercial vendor (Lonza) at passage 2.

    Article Title: Hyaluronic acid hydrogels support to generate integrated bone formation through endochondral ossification in vivo using mesenchymal stem cells.
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    Article Title: Hyaluronic acid hydrogels support to generate integrated bone formation through endochondral ossification in vivo using mesenchymal stem cells
    Article Snippet: Primary human bone marrow-derived MSCs (Lonza Japan, Tokyo) at passage two were expanded with MSCG Mesenchymal Stem Cell Growth Medium (Lonza Japan) at 37°C in 5% CO 2 and 95% humidified air, according to the manufacturer’s instructions.

    Article Title: Midazolam inhibits chondrogenesis via peripheral benzodiazepine receptor in human mesenchymal stem cells
    Article Snippet: We also purchased primary human bone marrow‐derived MSCs from Lonza Walksville Inc., which were maintained in growth medium: DMEM low glucose containing 10% foetal bovine serum (GIBCO with selected lot), 100 units/mL penicillin and 100 μg/mL streptomycin (both from GIBCO) at 37°C with a humidified 5% CO 2 atmosphere and medium was changed twice a week.

    Article Title: Multiple Myeloma-Derived Exosomes Regulate the Functions of Mesenchymal Stem Cells Partially via Modulating miR-21 and miR-146a
    Article Snippet: Primary human bone marrow-derived MSCs from healthy individuals were purchased from Lonza (Basel, Switzerland).

    Article Title: Role of Microtubules in Osteogenic Differentiation of Mesenchymal Stem Cells on 3D Nanofibrous Scaffolds.
    Article Snippet: Human bone marrow mesenchymal stem cells (MSCs) cultured on three-dimensional (3D) nanofibrous scaffolds are known to undergo osteogenic differentiation even in the absence of soluble osteoinductive factors.. While this process of differentiation has been attributed to the shape that cells assume on the fibrous scaffolds, it is unclear how constriction of cell shape would contribute to the differentiation phenotype.. Here, we quantitatively compared cell and nuclear morphologies of cells cultured on 3D poly(ε-caprolactone) (PCL) nanofibers (NF) and two-dimensional (2D) flat films using confocal fluorescence microscopy.

    Cell Culture:

    Article Title: Effects of organophosphates on the regulation of mesenchymal stem cell proliferation and differentiation.
    Article Snippet: Mesenchymal stem cells (MSCs) are multipotent cells located within various adult tissues.. Recent literature has reported that human bone marrow-derived MSCs express active acetylcholinesterase (AChE) and that disruption of AChE activity by organophosphate (OP) chemicals decreases the ability of MSCs to differentiate into osteoblasts.. The potential role of AChE in regulating MSC proliferation and differentiation is currently unknown.

    Article Title: The Effects of ROCK Inhibition on Mesenchymal Stem Cell Chondrogenesis Are Culture Model Dependent
    Article Snippet: Cell culture Primary human bone marrow-derived MSCs were purchased from a commercial vendor (Lonza) at passage 2.

    Article Title: The Effects of ROCK Inhibition on Mesenchymal Stem Cell Chondrogenesis Are Culture Model Dependent
    Article Snippet: Primary human bone marrow-derived MSCs were purchased from a commercial vendor (Lonza) at passage 2.

    Article Title: Hyaluronic acid hydrogels support to generate integrated bone formation through endochondral ossification in vivo using mesenchymal stem cells.
    Article Snippet: Primary human bone marrow-derived MSCs (Lonza Japan, Tokyo) at passage two were expanded with MSCG Mesenchymal Stem Cell Growth Medium (Lonza Japan) at 37 ̊C in 5% PLOS ONE | https://doi.org/10.1371/journal.pone.0281345 February 2, 2023 2 / 15 Funding: This work was supported by a Grant-inAid for Scientific Research (KAKENHI) from the Japan Society for the Promotion of Science (JSPS) (grant nos.

    Article Title: Hyaluronic acid hydrogels support to generate integrated bone formation through endochondral ossification in vivo using mesenchymal stem cells
    Article Snippet: Primary human bone marrow-derived MSCs (Lonza Japan, Tokyo) at passage two were expanded with MSCG Mesenchymal Stem Cell Growth Medium (Lonza Japan) at 37°C in 5% CO 2 and 95% humidified air, according to the manufacturer’s instructions.

    Article Title: Midazolam inhibits chondrogenesis via peripheral benzodiazepine receptor in human mesenchymal stem cells
    Article Snippet: We also purchased primary human bone marrow‐derived MSCs from Lonza Walksville Inc., which were maintained in growth medium: DMEM low glucose containing 10% foetal bovine serum (GIBCO with selected lot), 100 units/mL penicillin and 100 μg/mL streptomycin (both from GIBCO) at 37°C with a humidified 5% CO 2 atmosphere and medium was changed twice a week.

    Article Title: Multiple Myeloma-Derived Exosomes Regulate the Functions of Mesenchymal Stem Cells Partially via Modulating miR-21 and miR-146a
    Article Snippet: Primary human bone marrow-derived MSCs from healthy individuals were purchased from Lonza (Basel, Switzerland).

    Article Title: Role of Microtubules in Osteogenic Differentiation of Mesenchymal Stem Cells on 3D Nanofibrous Scaffolds.
    Article Snippet: Human bone marrow mesenchymal stem cells (MSCs) cultured on three-dimensional (3D) nanofibrous scaffolds are known to undergo osteogenic differentiation even in the absence of soluble osteoinductive factors.. While this process of differentiation has been attributed to the shape that cells assume on the fibrous scaffolds, it is unclear how constriction of cell shape would contribute to the differentiation phenotype.. Here, we quantitatively compared cell and nuclear morphologies of cells cultured on 3D poly(ε-caprolactone) (PCL) nanofibers (NF) and two-dimensional (2D) flat films using confocal fluorescence microscopy.

    Activity Assay:

    Article Title: Effects of organophosphates on the regulation of mesenchymal stem cell proliferation and differentiation.
    Article Snippet: Mesenchymal stem cells (MSCs) are multipotent cells located within various adult tissues.. Recent literature has reported that human bone marrow-derived MSCs express active acetylcholinesterase (AChE) and that disruption of AChE activity by organophosphate (OP) chemicals decreases the ability of MSCs to differentiate into osteoblasts.. The potential role of AChE in regulating MSC proliferation and differentiation is currently unknown.

    Article Title: The Effects of ROCK Inhibition on Mesenchymal Stem Cell Chondrogenesis Are Culture Model Dependent
    Article Snippet: Cell culture Primary human bone marrow-derived MSCs were purchased from a commercial vendor (Lonza) at passage 2.

    Article Title: The Effects of ROCK Inhibition on Mesenchymal Stem Cell Chondrogenesis Are Culture Model Dependent
    Article Snippet: Primary human bone marrow-derived MSCs were purchased from a commercial vendor (Lonza) at passage 2.

    Article Title: Hyaluronic acid hydrogels support to generate integrated bone formation through endochondral ossification in vivo using mesenchymal stem cells.
    Article Snippet: Primary human bone marrow-derived MSCs (Lonza Japan, Tokyo) at passage two were expanded with MSCG Mesenchymal Stem Cell Growth Medium (Lonza Japan) at 37 ̊C in 5% PLOS ONE | https://doi.org/10.1371/journal.pone.0281345 February 2, 2023 2 / 15 Funding: This work was supported by a Grant-inAid for Scientific Research (KAKENHI) from the Japan Society for the Promotion of Science (JSPS) (grant nos.

    Article Title: Hyaluronic acid hydrogels support to generate integrated bone formation through endochondral ossification in vivo using mesenchymal stem cells
    Article Snippet: Primary human bone marrow-derived MSCs (Lonza Japan, Tokyo) at passage two were expanded with MSCG Mesenchymal Stem Cell Growth Medium (Lonza Japan) at 37°C in 5% CO 2 and 95% humidified air, according to the manufacturer’s instructions.

    Article Title: Midazolam inhibits chondrogenesis via peripheral benzodiazepine receptor in human mesenchymal stem cells
    Article Snippet: We also purchased primary human bone marrow‐derived MSCs from Lonza Walksville Inc., which were maintained in growth medium: DMEM low glucose containing 10% foetal bovine serum (GIBCO with selected lot), 100 units/mL penicillin and 100 μg/mL streptomycin (both from GIBCO) at 37°C with a humidified 5% CO 2 atmosphere and medium was changed twice a week.

    Article Title: Multiple Myeloma-Derived Exosomes Regulate the Functions of Mesenchymal Stem Cells Partially via Modulating miR-21 and miR-146a
    Article Snippet: Primary human bone marrow-derived MSCs from healthy individuals were purchased from Lonza (Basel, Switzerland).

    Article Title: Role of Microtubules in Osteogenic Differentiation of Mesenchymal Stem Cells on 3D Nanofibrous Scaffolds.
    Article Snippet: Human bone marrow mesenchymal stem cells (MSCs) cultured on three-dimensional (3D) nanofibrous scaffolds are known to undergo osteogenic differentiation even in the absence of soluble osteoinductive factors.. While this process of differentiation has been attributed to the shape that cells assume on the fibrous scaffolds, it is unclear how constriction of cell shape would contribute to the differentiation phenotype.. Here, we quantitatively compared cell and nuclear morphologies of cells cultured on 3D poly(ε-caprolactone) (PCL) nanofibers (NF) and two-dimensional (2D) flat films using confocal fluorescence microscopy.

    AChE Assay:

    Article Title: Effects of organophosphates on the regulation of mesenchymal stem cell proliferation and differentiation.
    Article Snippet: Mesenchymal stem cells (MSCs) are multipotent cells located within various adult tissues.. Recent literature has reported that human bone marrow-derived MSCs express active acetylcholinesterase (AChE) and that disruption of AChE activity by organophosphate (OP) chemicals decreases the ability of MSCs to differentiate into osteoblasts.. The potential role of AChE in regulating MSC proliferation and differentiation is currently unknown.

    Article Title: The Effects of ROCK Inhibition on Mesenchymal Stem Cell Chondrogenesis Are Culture Model Dependent
    Article Snippet: Cell culture Primary human bone marrow-derived MSCs were purchased from a commercial vendor (Lonza) at passage 2.

    Article Title: The Effects of ROCK Inhibition on Mesenchymal Stem Cell Chondrogenesis Are Culture Model Dependent
    Article Snippet: Primary human bone marrow-derived MSCs were purchased from a commercial vendor (Lonza) at passage 2.

    Article Title: Hyaluronic acid hydrogels support to generate integrated bone formation through endochondral ossification in vivo using mesenchymal stem cells.
    Article Snippet: Primary human bone marrow-derived MSCs (Lonza Japan, Tokyo) at passage two were expanded with MSCG Mesenchymal Stem Cell Growth Medium (Lonza Japan) at 37 ̊C in 5% PLOS ONE | https://doi.org/10.1371/journal.pone.0281345 February 2, 2023 2 / 15 Funding: This work was supported by a Grant-inAid for Scientific Research (KAKENHI) from the Japan Society for the Promotion of Science (JSPS) (grant nos.

    Article Title: Hyaluronic acid hydrogels support to generate integrated bone formation through endochondral ossification in vivo using mesenchymal stem cells
    Article Snippet: Primary human bone marrow-derived MSCs (Lonza Japan, Tokyo) at passage two were expanded with MSCG Mesenchymal Stem Cell Growth Medium (Lonza Japan) at 37°C in 5% CO 2 and 95% humidified air, according to the manufacturer’s instructions.

    Article Title: Midazolam inhibits chondrogenesis via peripheral benzodiazepine receptor in human mesenchymal stem cells
    Article Snippet: We also purchased primary human bone marrow‐derived MSCs from Lonza Walksville Inc., which were maintained in growth medium: DMEM low glucose containing 10% foetal bovine serum (GIBCO with selected lot), 100 units/mL penicillin and 100 μg/mL streptomycin (both from GIBCO) at 37°C with a humidified 5% CO 2 atmosphere and medium was changed twice a week.

    Article Title: Multiple Myeloma-Derived Exosomes Regulate the Functions of Mesenchymal Stem Cells Partially via Modulating miR-21 and miR-146a
    Article Snippet: Primary human bone marrow-derived MSCs from healthy individuals were purchased from Lonza (Basel, Switzerland).

    Article Title: Role of Microtubules in Osteogenic Differentiation of Mesenchymal Stem Cells on 3D Nanofibrous Scaffolds.
    Article Snippet: Human bone marrow mesenchymal stem cells (MSCs) cultured on three-dimensional (3D) nanofibrous scaffolds are known to undergo osteogenic differentiation even in the absence of soluble osteoinductive factors.. While this process of differentiation has been attributed to the shape that cells assume on the fibrous scaffolds, it is unclear how constriction of cell shape would contribute to the differentiation phenotype.. Here, we quantitatively compared cell and nuclear morphologies of cells cultured on 3D poly(ε-caprolactone) (PCL) nanofibers (NF) and two-dimensional (2D) flat films using confocal fluorescence microscopy.

    Radio Immunoprecipitation:

    Article Title: Effects of organophosphates on the regulation of mesenchymal stem cell proliferation and differentiation.
    Article Snippet: Mesenchymal stem cells (MSCs) are multipotent cells located within various adult tissues.. Recent literature has reported that human bone marrow-derived MSCs express active acetylcholinesterase (AChE) and that disruption of AChE activity by organophosphate (OP) chemicals decreases the ability of MSCs to differentiate into osteoblasts.. The potential role of AChE in regulating MSC proliferation and differentiation is currently unknown.

    Article Title: The Effects of ROCK Inhibition on Mesenchymal Stem Cell Chondrogenesis Are Culture Model Dependent
    Article Snippet: Cell culture Primary human bone marrow-derived MSCs were purchased from a commercial vendor (Lonza) at passage 2.

    Article Title: The Effects of ROCK Inhibition on Mesenchymal Stem Cell Chondrogenesis Are Culture Model Dependent
    Article Snippet: Primary human bone marrow-derived MSCs were purchased from a commercial vendor (Lonza) at passage 2.

    Article Title: Hyaluronic acid hydrogels support to generate integrated bone formation through endochondral ossification in vivo using mesenchymal stem cells.
    Article Snippet: Primary human bone marrow-derived MSCs (Lonza Japan, Tokyo) at passage two were expanded with MSCG Mesenchymal Stem Cell Growth Medium (Lonza Japan) at 37 ̊C in 5% PLOS ONE | https://doi.org/10.1371/journal.pone.0281345 February 2, 2023 2 / 15 Funding: This work was supported by a Grant-inAid for Scientific Research (KAKENHI) from the Japan Society for the Promotion of Science (JSPS) (grant nos.

    Article Title: Hyaluronic acid hydrogels support to generate integrated bone formation through endochondral ossification in vivo using mesenchymal stem cells
    Article Snippet: Primary human bone marrow-derived MSCs (Lonza Japan, Tokyo) at passage two were expanded with MSCG Mesenchymal Stem Cell Growth Medium (Lonza Japan) at 37°C in 5% CO 2 and 95% humidified air, according to the manufacturer’s instructions.

    Article Title: Midazolam inhibits chondrogenesis via peripheral benzodiazepine receptor in human mesenchymal stem cells
    Article Snippet: We also purchased primary human bone marrow‐derived MSCs from Lonza Walksville Inc., which were maintained in growth medium: DMEM low glucose containing 10% foetal bovine serum (GIBCO with selected lot), 100 units/mL penicillin and 100 μg/mL streptomycin (both from GIBCO) at 37°C with a humidified 5% CO 2 atmosphere and medium was changed twice a week.

    Article Title: Multiple Myeloma-Derived Exosomes Regulate the Functions of Mesenchymal Stem Cells Partially via Modulating miR-21 and miR-146a
    Article Snippet: Primary human bone marrow-derived MSCs from healthy individuals were purchased from Lonza (Basel, Switzerland).

    Article Title: Role of Microtubules in Osteogenic Differentiation of Mesenchymal Stem Cells on 3D Nanofibrous Scaffolds.
    Article Snippet: Human bone marrow mesenchymal stem cells (MSCs) cultured on three-dimensional (3D) nanofibrous scaffolds are known to undergo osteogenic differentiation even in the absence of soluble osteoinductive factors.. While this process of differentiation has been attributed to the shape that cells assume on the fibrous scaffolds, it is unclear how constriction of cell shape would contribute to the differentiation phenotype.. Here, we quantitatively compared cell and nuclear morphologies of cells cultured on 3D poly(ε-caprolactone) (PCL) nanofibers (NF) and two-dimensional (2D) flat films using confocal fluorescence microscopy.

    Protein Concentration:

    Article Title: Effects of organophosphates on the regulation of mesenchymal stem cell proliferation and differentiation.
    Article Snippet: Mesenchymal stem cells (MSCs) are multipotent cells located within various adult tissues.. Recent literature has reported that human bone marrow-derived MSCs express active acetylcholinesterase (AChE) and that disruption of AChE activity by organophosphate (OP) chemicals decreases the ability of MSCs to differentiate into osteoblasts.. The potential role of AChE in regulating MSC proliferation and differentiation is currently unknown.

    Article Title: The Effects of ROCK Inhibition on Mesenchymal Stem Cell Chondrogenesis Are Culture Model Dependent
    Article Snippet: Cell culture Primary human bone marrow-derived MSCs were purchased from a commercial vendor (Lonza) at passage 2.

    Article Title: The Effects of ROCK Inhibition on Mesenchymal Stem Cell Chondrogenesis Are Culture Model Dependent
    Article Snippet: Primary human bone marrow-derived MSCs were purchased from a commercial vendor (Lonza) at passage 2.

    Article Title: Hyaluronic acid hydrogels support to generate integrated bone formation through endochondral ossification in vivo using mesenchymal stem cells.
    Article Snippet: Primary human bone marrow-derived MSCs (Lonza Japan, Tokyo) at passage two were expanded with MSCG Mesenchymal Stem Cell Growth Medium (Lonza Japan) at 37 ̊C in 5% PLOS ONE | https://doi.org/10.1371/journal.pone.0281345 February 2, 2023 2 / 15 Funding: This work was supported by a Grant-inAid for Scientific Research (KAKENHI) from the Japan Society for the Promotion of Science (JSPS) (grant nos.

    Article Title: Hyaluronic acid hydrogels support to generate integrated bone formation through endochondral ossification in vivo using mesenchymal stem cells
    Article Snippet: Primary human bone marrow-derived MSCs (Lonza Japan, Tokyo) at passage two were expanded with MSCG Mesenchymal Stem Cell Growth Medium (Lonza Japan) at 37°C in 5% CO 2 and 95% humidified air, according to the manufacturer’s instructions.

    Article Title: Midazolam inhibits chondrogenesis via peripheral benzodiazepine receptor in human mesenchymal stem cells
    Article Snippet: We also purchased primary human bone marrow‐derived MSCs from Lonza Walksville Inc., which were maintained in growth medium: DMEM low glucose containing 10% foetal bovine serum (GIBCO with selected lot), 100 units/mL penicillin and 100 μg/mL streptomycin (both from GIBCO) at 37°C with a humidified 5% CO 2 atmosphere and medium was changed twice a week.

    Article Title: Multiple Myeloma-Derived Exosomes Regulate the Functions of Mesenchymal Stem Cells Partially via Modulating miR-21 and miR-146a
    Article Snippet: Primary human bone marrow-derived MSCs from healthy individuals were purchased from Lonza (Basel, Switzerland).

    Article Title: Role of Microtubules in Osteogenic Differentiation of Mesenchymal Stem Cells on 3D Nanofibrous Scaffolds.
    Article Snippet: Human bone marrow mesenchymal stem cells (MSCs) cultured on three-dimensional (3D) nanofibrous scaffolds are known to undergo osteogenic differentiation even in the absence of soluble osteoinductive factors.. While this process of differentiation has been attributed to the shape that cells assume on the fibrous scaffolds, it is unclear how constriction of cell shape would contribute to the differentiation phenotype.. Here, we quantitatively compared cell and nuclear morphologies of cells cultured on 3D poly(ε-caprolactone) (PCL) nanofibers (NF) and two-dimensional (2D) flat films using confocal fluorescence microscopy.



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    Mesenchymal stromal cells enhances stemness and chemoresistance of gastric cancer cells. A-E: The MKN45 and AGS cells were co-cultured with mesenchymal stromal cells (MSCs); The stemness was analyzed using sphere formation assay (A); The mRNA expression of SOX2, Oct4, LIN28, and CD133 was measured by qPCR (B); The levels of SOX2, Oct4, LIN28, and CD133 was detected by Western blot analysis (C); The CD44+ and CD133+ cells were identified by flow cytometry analysis (D and E); F and G: The MKN45 and AGS cells were co-cultured with MSCs and treated with oxaliplatin or 5-Fu; The cell apoptosis was determined by flow cytometry analysis (F); The cell proliferation was examined by colony formation assay (G). a P < 0.01; MSC: Mesenchymal stromal cell.

    Journal: World Journal of Gastrointestinal Oncology

    Article Title: Mesenchymal stem cell-derived lncRNAs NKILA contributes to stemness and chemoresistance by fatty acid oxidation in gastric cancer via miR-485-5p/STAT3

    doi: 10.4251/wjgo.v17.i8.105006

    Figure Lengend Snippet: Mesenchymal stromal cells enhances stemness and chemoresistance of gastric cancer cells. A-E: The MKN45 and AGS cells were co-cultured with mesenchymal stromal cells (MSCs); The stemness was analyzed using sphere formation assay (A); The mRNA expression of SOX2, Oct4, LIN28, and CD133 was measured by qPCR (B); The levels of SOX2, Oct4, LIN28, and CD133 was detected by Western blot analysis (C); The CD44+ and CD133+ cells were identified by flow cytometry analysis (D and E); F and G: The MKN45 and AGS cells were co-cultured with MSCs and treated with oxaliplatin or 5-Fu; The cell apoptosis was determined by flow cytometry analysis (F); The cell proliferation was examined by colony formation assay (G). a P < 0.01; MSC: Mesenchymal stromal cell.

    Article Snippet: Primary human bone marrow-derived MSCs (HUXMA-01001, Procell, China) were cultured in α-MEM medium (Hyclone, United States) supplemented with 10% FBS and 1% penicillin/streptomycin.

    Techniques: Cell Culture, Tube Formation Assay, Expressing, Western Blot, Flow Cytometry, Colony Assay

    Effect of different donor-derived human peripheral blood mononuclear cells (PBMCs) on the in vitro immunomodulatory response of bone marrow (BM)- mesenchymal stem cells (MSCs). (a) Schematic of the protocol for lymphocyte proliferation assays with mitogen as an immunomodulatory potency assay for MSCs. (b) Proliferation of 10 donor-derived PBMCs upon phytohemagglutinin (PHA; 0.2, 0.5, and 1.0 μg/mL) stimulation was assessed through BrdU uptake. BrdU uptake was indicated by luminescence signal (counts per second, CPS). Two-way ANOVA showed that PBMCs proliferation was significantly affected by the stimulating PHA concentration, the presence or absence of MSCs, and their interaction (p < 0.0001). All values indicate the mean ± standard deviation of mean of three biological replicates (n = 3) (∗P < 0.05, ∗∗P < 0.01, ∗∗∗∗P < 0.0001, two-way analysis of variance, followed by Bonferroni's multiple comparison test). (c) Effect of PBMCs derived from 10 donors on the in vitro immunomodulatory response of BM-MSCs. The rate of suppression by BM-MSCs on PBMC proliferation stimulated with three PHA concentrations (0.2, 0.5, and 1.0 μg/mL) is shown as the immunosuppression rate; CPS(PBMC + MSC)/CPS(PBMC).

    Journal: Regenerative Therapy

    Article Title: Increasing robustness of in vitro assay for immnosuppressive effect of mesenchymal stromal/stem cells: The role of inflammatory cytokine production by peripheral blood mononuclear cells

    doi: 10.1016/j.reth.2024.12.016

    Figure Lengend Snippet: Effect of different donor-derived human peripheral blood mononuclear cells (PBMCs) on the in vitro immunomodulatory response of bone marrow (BM)- mesenchymal stem cells (MSCs). (a) Schematic of the protocol for lymphocyte proliferation assays with mitogen as an immunomodulatory potency assay for MSCs. (b) Proliferation of 10 donor-derived PBMCs upon phytohemagglutinin (PHA; 0.2, 0.5, and 1.0 μg/mL) stimulation was assessed through BrdU uptake. BrdU uptake was indicated by luminescence signal (counts per second, CPS). Two-way ANOVA showed that PBMCs proliferation was significantly affected by the stimulating PHA concentration, the presence or absence of MSCs, and their interaction (p < 0.0001). All values indicate the mean ± standard deviation of mean of three biological replicates (n = 3) (∗P < 0.05, ∗∗P < 0.01, ∗∗∗∗P < 0.0001, two-way analysis of variance, followed by Bonferroni's multiple comparison test). (c) Effect of PBMCs derived from 10 donors on the in vitro immunomodulatory response of BM-MSCs. The rate of suppression by BM-MSCs on PBMC proliferation stimulated with three PHA concentrations (0.2, 0.5, and 1.0 μg/mL) is shown as the immunosuppression rate; CPS(PBMC + MSC)/CPS(PBMC).

    Article Snippet: Primary human bone marrow-derived MSCs (BM-MSC) were purchased from Lonza (Walkersville, MD, USA) (PT-2501).

    Techniques: Derivative Assay, In Vitro, Potency Assay, Concentration Assay, Standard Deviation, Comparison

    Relationship between the production of cytokines by PHA-stimulated PBMCs and the suppression rate of PBMC proliferation by MSCs in the immunomodulatory potency assay. Spearman correlation analysis between the concentration of each cytokine in the culture supernatant when PBMCs were stimulated with 1.0 μg/mL PHA and the rate of proliferation inhibition by BM-MSCs in the immunomodulatory potency assay is shown with linear regression lines and their 95 % confidential intervals. r, correlation coefficient.

    Journal: Regenerative Therapy

    Article Title: Increasing robustness of in vitro assay for immnosuppressive effect of mesenchymal stromal/stem cells: The role of inflammatory cytokine production by peripheral blood mononuclear cells

    doi: 10.1016/j.reth.2024.12.016

    Figure Lengend Snippet: Relationship between the production of cytokines by PHA-stimulated PBMCs and the suppression rate of PBMC proliferation by MSCs in the immunomodulatory potency assay. Spearman correlation analysis between the concentration of each cytokine in the culture supernatant when PBMCs were stimulated with 1.0 μg/mL PHA and the rate of proliferation inhibition by BM-MSCs in the immunomodulatory potency assay is shown with linear regression lines and their 95 % confidential intervals. r, correlation coefficient.

    Article Snippet: Primary human bone marrow-derived MSCs (BM-MSC) were purchased from Lonza (Walkersville, MD, USA) (PT-2501).

    Techniques: Potency Assay, Concentration Assay, Inhibition

    Inter-test variability in the rate of proliferation inhibition of PBMCs by repeated one-way MLR assay.

    Journal: Regenerative Therapy

    Article Title: Increasing robustness of in vitro assay for immnosuppressive effect of mesenchymal stromal/stem cells: The role of inflammatory cytokine production by peripheral blood mononuclear cells

    doi: 10.1016/j.reth.2024.12.016

    Figure Lengend Snippet: Inter-test variability in the rate of proliferation inhibition of PBMCs by repeated one-way MLR assay.

    Article Snippet: Primary human bone marrow-derived MSCs (BM-MSC) were purchased from Lonza (Walkersville, MD, USA) (PT-2501).

    Techniques: Inhibition, Mlr Assay

    Figure summarizing the flow of the reversed effects of MSCs depending on the cytokine production concentration of PHA-stimulated PBMCs in the immunomodulatory potency assay. The illustration of MSC in the figure was done using BioRender: scientific image and illustration software.

    Journal: Regenerative Therapy

    Article Title: Increasing robustness of in vitro assay for immnosuppressive effect of mesenchymal stromal/stem cells: The role of inflammatory cytokine production by peripheral blood mononuclear cells

    doi: 10.1016/j.reth.2024.12.016

    Figure Lengend Snippet: Figure summarizing the flow of the reversed effects of MSCs depending on the cytokine production concentration of PHA-stimulated PBMCs in the immunomodulatory potency assay. The illustration of MSC in the figure was done using BioRender: scientific image and illustration software.

    Article Snippet: Primary human bone marrow-derived MSCs (BM-MSC) were purchased from Lonza (Walkersville, MD, USA) (PT-2501).

    Techniques: Concentration Assay, Potency Assay, Software

    Endocytosis of EVs by HMSCs (A) Representative confocal micrograph of fluorescently labeled fresh and lyophilized BMP2 EVs (green) endocytosed by naïve HMSCs at 37°C. Scale bar = 20 μm. (B) Dose-dependent endocytosis of fresh and lyophilized BMP2 EVs by HMSCs. Data points represent mean percentage fluorescence ± SD (n = 6). (C) Graph showing the inhibition of EV endocytosis after pre-treatment of the EVs with heparin to block interaction with the cell surface HSPGs. The reduction of EV endocytosis at 4°C was also measured compared to 37°C. Data represent mean percentage fluorescence with respect to control ± SD (n = 6). *: statistical significance with respect to No blocking control, #: statistical significance with respect to BMP2 EV group as measured by Student’s t-test (P< 0.05).

    Journal: Frontiers in Bioengineering and Biotechnology

    Article Title: Functionality of lyophilized osteoinductive EVs: a mechanistic study

    doi: 10.3389/fbioe.2024.1452428

    Figure Lengend Snippet: Endocytosis of EVs by HMSCs (A) Representative confocal micrograph of fluorescently labeled fresh and lyophilized BMP2 EVs (green) endocytosed by naïve HMSCs at 37°C. Scale bar = 20 μm. (B) Dose-dependent endocytosis of fresh and lyophilized BMP2 EVs by HMSCs. Data points represent mean percentage fluorescence ± SD (n = 6). (C) Graph showing the inhibition of EV endocytosis after pre-treatment of the EVs with heparin to block interaction with the cell surface HSPGs. The reduction of EV endocytosis at 4°C was also measured compared to 37°C. Data represent mean percentage fluorescence with respect to control ± SD (n = 6). *: statistical significance with respect to No blocking control, #: statistical significance with respect to BMP2 EV group as measured by Student’s t-test (P< 0.05).

    Article Snippet: Primary human bone marrow derived MSCs (HMSCs) were purchased from Lonza and cultured in αMEM basal media (Gibco) supplemented with 20% fetal bovine serum (FBS, Gibco), 1% (v/v) L-Glutamine (Gibco) and 1% (v/v) antibiotic-antimycotic solution (Gibco).

    Techniques: Labeling, Fluorescence, Inhibition, Blocking Assay, Control

    Osteoinductive property of the lyophilized BMP2 EVs (A) Osteoinductive gene expression levels in fresh and lyophilized BMP2 EV HMSCs at day 3 and 5 with respect to control (no EV) group. Data are represented as mean fold changes ± SD (n = 4). *: statistical significance with respect to BMP2 EV group as measured by student’s t-test (P< 0.05). (B) Graph representing relative luciferase activity in HMSCs transfected with a BMP2 reporter luciferase plasmid (n = 4). Recombinant BMP2 protein (BMP2 GF) was used as positive control. Note the significant increase in luciferase activity in fresh and lyophilized BMP2 EV treated groups compared to control. *: statistical significance with respect to control, #: statistical significance with respect to BMP2 GF group as measured by Tukey’s test post ANOVA (P< 0.05). (C) Graph representing relative alkaline phosphatase (ALP) activity in HMSCs treated with osteogenic differentiation medium (OS) in the presence/absence of fresh and lyophilized BMP2 EVs at 3 and 7 days (n = 4). *: statistical significance with respect to control, #: statistical significance with respect to OS + BMP2 EV group as measured by Student’s t-test (P< 0.05). (D) Quantitative in-cell western for the presence of phosphorylated SMAD 1/5/8 and the corresponding tubulin expression in a 96 well plate assay (n = 6). The graph represents quantitation of the fluorescence from the wells using the LICOR Odyssey imager normalized to tubulin. *: statistical significance with respect to control group as measured by Tukey’s test post ANOVA (P< 0.05).

    Journal: Frontiers in Bioengineering and Biotechnology

    Article Title: Functionality of lyophilized osteoinductive EVs: a mechanistic study

    doi: 10.3389/fbioe.2024.1452428

    Figure Lengend Snippet: Osteoinductive property of the lyophilized BMP2 EVs (A) Osteoinductive gene expression levels in fresh and lyophilized BMP2 EV HMSCs at day 3 and 5 with respect to control (no EV) group. Data are represented as mean fold changes ± SD (n = 4). *: statistical significance with respect to BMP2 EV group as measured by student’s t-test (P< 0.05). (B) Graph representing relative luciferase activity in HMSCs transfected with a BMP2 reporter luciferase plasmid (n = 4). Recombinant BMP2 protein (BMP2 GF) was used as positive control. Note the significant increase in luciferase activity in fresh and lyophilized BMP2 EV treated groups compared to control. *: statistical significance with respect to control, #: statistical significance with respect to BMP2 GF group as measured by Tukey’s test post ANOVA (P< 0.05). (C) Graph representing relative alkaline phosphatase (ALP) activity in HMSCs treated with osteogenic differentiation medium (OS) in the presence/absence of fresh and lyophilized BMP2 EVs at 3 and 7 days (n = 4). *: statistical significance with respect to control, #: statistical significance with respect to OS + BMP2 EV group as measured by Student’s t-test (P< 0.05). (D) Quantitative in-cell western for the presence of phosphorylated SMAD 1/5/8 and the corresponding tubulin expression in a 96 well plate assay (n = 6). The graph represents quantitation of the fluorescence from the wells using the LICOR Odyssey imager normalized to tubulin. *: statistical significance with respect to control group as measured by Tukey’s test post ANOVA (P< 0.05).

    Article Snippet: Primary human bone marrow derived MSCs (HMSCs) were purchased from Lonza and cultured in αMEM basal media (Gibco) supplemented with 20% fetal bovine serum (FBS, Gibco), 1% (v/v) L-Glutamine (Gibco) and 1% (v/v) antibiotic-antimycotic solution (Gibco).

    Techniques: Gene Expression, Control, Luciferase, Activity Assay, Transfection, Plasmid Preparation, Recombinant, Positive Control, In-Cell ELISA, Expressing, Quantitation Assay, Fluorescence

    Binding of lyophilized EVs to ECM proteins (A) Representative confocal image showing the binding of fluorescently labeled lyophilized EVs (green) to the decellularized ECM of HMSCs. Counterstain was performed for type I collagen (red, scale bar = 5 μm). (B) Dose-dependent binding of fluorescently labeled lyophilized EVs to type I collagen coated assay plates (data points represent mean ± SD, n = 6). (C) Representative confocal image showing the binding of fluorescently labeled lyophilized EVs (green) to the decellularized ECM of HMSCs. Counterstain was performed for fibronectin (red, scale bar = 20 μm). (D) Dose-dependent binding of fluorescently labeled lyophilized EVs to fibronectin coated assay plates (data points represent mean ± SD, n = 6).

    Journal: Frontiers in Bioengineering and Biotechnology

    Article Title: Functionality of lyophilized osteoinductive EVs: a mechanistic study

    doi: 10.3389/fbioe.2024.1452428

    Figure Lengend Snippet: Binding of lyophilized EVs to ECM proteins (A) Representative confocal image showing the binding of fluorescently labeled lyophilized EVs (green) to the decellularized ECM of HMSCs. Counterstain was performed for type I collagen (red, scale bar = 5 μm). (B) Dose-dependent binding of fluorescently labeled lyophilized EVs to type I collagen coated assay plates (data points represent mean ± SD, n = 6). (C) Representative confocal image showing the binding of fluorescently labeled lyophilized EVs (green) to the decellularized ECM of HMSCs. Counterstain was performed for fibronectin (red, scale bar = 20 μm). (D) Dose-dependent binding of fluorescently labeled lyophilized EVs to fibronectin coated assay plates (data points represent mean ± SD, n = 6).

    Article Snippet: Primary human bone marrow derived MSCs (HMSCs) were purchased from Lonza and cultured in αMEM basal media (Gibco) supplemented with 20% fetal bovine serum (FBS, Gibco), 1% (v/v) L-Glutamine (Gibco) and 1% (v/v) antibiotic-antimycotic solution (Gibco).

    Techniques: Binding Assay, Labeling

    Fig. 1. Screening of cytokines and small molecules for LSEC differentiation. (A) The schematic representation of BM-MSC differentiation. (B) qPCR analysis of the expression levels of LYVE1 and CD36 in BM-MSC-derived cells. On the y-axis, the expression levels are shown as a relative value to those of BM-MSCs. All data are presented as mean ± SD (n ¼ 3). Significant differences were evaluated using a one-way ANOVA followed by Dunnett's post-hoc test (*p < 0.05, ***p < 0.001 compared with BFTc [BMP4, FGF8b, TGF-b inhibitor, and cAMP]). Abbreviations: B; BMP4, F; FGF8b, T; TGF-b signal inhibitor, c; cAMP.

    Journal: Regenerative therapy

    Article Title: Generation of functional liver sinusoidal endothelial-like cells from human bone marrow-derived mesenchymal stem cells.

    doi: 10.1016/j.reth.2023.07.006

    Figure Lengend Snippet: Fig. 1. Screening of cytokines and small molecules for LSEC differentiation. (A) The schematic representation of BM-MSC differentiation. (B) qPCR analysis of the expression levels of LYVE1 and CD36 in BM-MSC-derived cells. On the y-axis, the expression levels are shown as a relative value to those of BM-MSCs. All data are presented as mean ± SD (n ¼ 3). Significant differences were evaluated using a one-way ANOVA followed by Dunnett's post-hoc test (*p < 0.05, ***p < 0.001 compared with BFTc [BMP4, FGF8b, TGF-b inhibitor, and cAMP]). Abbreviations: B; BMP4, F; FGF8b, T; TGF-b signal inhibitor, c; cAMP.

    Article Snippet: Primary human bone marrow-derived MSCs (C-12974; PromoCell) were cultured in Mesenchymal Stem Cell Growth Medium 2 (C-28009; PromoCell).

    Techniques: Expressing, Derivative Assay

    Fig. 2. Analysis of the expression of LSEC-related markers. (A) The schematic representation of BM-MSC differentiation to LSEC-like cells. (B) Brightfield images of the BM-MSCs and BM-MSC-derived cells. Scale bar ¼ 500 mm. (C) qPCR analysis of gene expression of LYVE1, CD36, CD32b, F8, PLVAP, CD31, and VEGFR2 in the BM-MSCs and BM-MSC-derived cells. On the y-axis, the expression levels are shown as a relative value to those of BM-MSCs. Data are presented as mean ± SD (n ¼ 6, sum of two independent experiments, n ¼ 3 for each experiment). (D) Immunocytochemistry analysis of LYVE1 (green) and CD36 (red) in the BM-MSCs and BM-MSC-derived cells. The nuclei were counterstained with DAPI (blue). Scale bar ¼ 50 mm. (E) The expression level of CD32 in the BM-MSCs and BM-MSC-derived cells was measured using flow cytometry analysis. The values of mean fluorescence intensity (MFI) of CD32 expression were normalized by the MFI of isotype control. Data are presented as mean ± SD (n ¼ 3). Significant differences were evaluated using an unpaired two-tailed Student's t-test (***p < 0.001). (F) The percentage of LYVE1- or CD36-positive cells in the BM-MSC-derived cells was measured using flow cytometry analysis.

    Journal: Regenerative therapy

    Article Title: Generation of functional liver sinusoidal endothelial-like cells from human bone marrow-derived mesenchymal stem cells.

    doi: 10.1016/j.reth.2023.07.006

    Figure Lengend Snippet: Fig. 2. Analysis of the expression of LSEC-related markers. (A) The schematic representation of BM-MSC differentiation to LSEC-like cells. (B) Brightfield images of the BM-MSCs and BM-MSC-derived cells. Scale bar ¼ 500 mm. (C) qPCR analysis of gene expression of LYVE1, CD36, CD32b, F8, PLVAP, CD31, and VEGFR2 in the BM-MSCs and BM-MSC-derived cells. On the y-axis, the expression levels are shown as a relative value to those of BM-MSCs. Data are presented as mean ± SD (n ¼ 6, sum of two independent experiments, n ¼ 3 for each experiment). (D) Immunocytochemistry analysis of LYVE1 (green) and CD36 (red) in the BM-MSCs and BM-MSC-derived cells. The nuclei were counterstained with DAPI (blue). Scale bar ¼ 50 mm. (E) The expression level of CD32 in the BM-MSCs and BM-MSC-derived cells was measured using flow cytometry analysis. The values of mean fluorescence intensity (MFI) of CD32 expression were normalized by the MFI of isotype control. Data are presented as mean ± SD (n ¼ 3). Significant differences were evaluated using an unpaired two-tailed Student's t-test (***p < 0.001). (F) The percentage of LYVE1- or CD36-positive cells in the BM-MSC-derived cells was measured using flow cytometry analysis.

    Article Snippet: Primary human bone marrow-derived MSCs (C-12974; PromoCell) were cultured in Mesenchymal Stem Cell Growth Medium 2 (C-28009; PromoCell).

    Techniques: Expressing, Derivative Assay, Gene Expression, Immunocytochemistry, Cytometry, Control, Two Tailed Test

    Fig. 3. Evaluation of endothelial cell-related functions. (A) Tube-formation assay of the BM-MSCs, BM-MSC-derived cells, and HUVECs. Scale bar ¼ 200 mm. (B) acLDL-uptake assay. BM-MSCs, BM-MSC-derived cells, and HUVECs were cultured in a medium containing Alexa Fluor 488-conjugated acLDL to measure their ability to take up acLDL. Scale bar ¼ 20 mm. Abbreviation: LDL, low-density lipoprotein.

    Journal: Regenerative therapy

    Article Title: Generation of functional liver sinusoidal endothelial-like cells from human bone marrow-derived mesenchymal stem cells.

    doi: 10.1016/j.reth.2023.07.006

    Figure Lengend Snippet: Fig. 3. Evaluation of endothelial cell-related functions. (A) Tube-formation assay of the BM-MSCs, BM-MSC-derived cells, and HUVECs. Scale bar ¼ 200 mm. (B) acLDL-uptake assay. BM-MSCs, BM-MSC-derived cells, and HUVECs were cultured in a medium containing Alexa Fluor 488-conjugated acLDL to measure their ability to take up acLDL. Scale bar ¼ 20 mm. Abbreviation: LDL, low-density lipoprotein.

    Article Snippet: Primary human bone marrow-derived MSCs (C-12974; PromoCell) were cultured in Mesenchymal Stem Cell Growth Medium 2 (C-28009; PromoCell).

    Techniques: Tube Formation Assay, Derivative Assay, Cell Culture

    Fig. 4. Evaluation of LSEC-related functions. (A) HA-uptake assay. BM-MSCs, BM-MSC-derived cells, and HUVECs were cultured in a medium containing fluoresceinamine- conjugated HA to measure their ability to take up HA. (B) IgG-uptake assay. BM-MSCs, BM-MSC-derived cells, and HUVECs were cultured in a medium containing Alexa Fluor 488-conjugated IgG to measure their ability to endocytose IgG. Scale bar ¼ 20 mm. Abbreviation: HA, hyaluronic acid.

    Journal: Regenerative therapy

    Article Title: Generation of functional liver sinusoidal endothelial-like cells from human bone marrow-derived mesenchymal stem cells.

    doi: 10.1016/j.reth.2023.07.006

    Figure Lengend Snippet: Fig. 4. Evaluation of LSEC-related functions. (A) HA-uptake assay. BM-MSCs, BM-MSC-derived cells, and HUVECs were cultured in a medium containing fluoresceinamine- conjugated HA to measure their ability to take up HA. (B) IgG-uptake assay. BM-MSCs, BM-MSC-derived cells, and HUVECs were cultured in a medium containing Alexa Fluor 488-conjugated IgG to measure their ability to endocytose IgG. Scale bar ¼ 20 mm. Abbreviation: HA, hyaluronic acid.

    Article Snippet: Primary human bone marrow-derived MSCs (C-12974; PromoCell) were cultured in Mesenchymal Stem Cell Growth Medium 2 (C-28009; PromoCell).

    Techniques: Derivative Assay, Cell Culture

    Fig. 5. Evaluation of the differentiation capacity of primary human BM-MSCs into LSEC-like cells (A) The schematic representation of the differentiation of primary human BM- MSCs into LSEC-like cells. (B) qPCR analysis of gene expression of LYVE1, CD36, CD32b, and F8 in primary human BM-MSCs and primary human BM-MSC-derived cells. On the y-axis, the expression levels are shown as a relative value to those of primary human BM-MSCs. Data are presented as mean ± SD (n 8, sum of two independent experiments, n 3 for each experiment.). Significant differences were evaluated using an unpaired two-tailed Student's t-test (*p < 0.05, ***p < 0.001). (C) The percentage of LYVE1- or CD36- positive cells in the primary human BM-MSC-derived cells was measured using flow cytometry analysis. Data are presented as mean ± SD (n ¼ 3). (D) acLDL-uptake assay. BM-MSCs, BM-MSC-derived cells, and HUVECs were cultured in a medium containing Alexa Fluor 488-conjugated acLDL to measure their ability to take up acLDL. Scale bar ¼ 20 mm. (E) HA- uptake assay. Primary human BM-MSCs and primary human BM-MSC-derived cells were cultured in a medium containing fluoresceinamine-conjugated HA to measure their ability to take up HA. Scale bar ¼ 20 mm. Abbreviation: LDL, low-density lipoprotein; HA, hyaluronic acid.

    Journal: Regenerative therapy

    Article Title: Generation of functional liver sinusoidal endothelial-like cells from human bone marrow-derived mesenchymal stem cells.

    doi: 10.1016/j.reth.2023.07.006

    Figure Lengend Snippet: Fig. 5. Evaluation of the differentiation capacity of primary human BM-MSCs into LSEC-like cells (A) The schematic representation of the differentiation of primary human BM- MSCs into LSEC-like cells. (B) qPCR analysis of gene expression of LYVE1, CD36, CD32b, and F8 in primary human BM-MSCs and primary human BM-MSC-derived cells. On the y-axis, the expression levels are shown as a relative value to those of primary human BM-MSCs. Data are presented as mean ± SD (n 8, sum of two independent experiments, n 3 for each experiment.). Significant differences were evaluated using an unpaired two-tailed Student's t-test (*p < 0.05, ***p < 0.001). (C) The percentage of LYVE1- or CD36- positive cells in the primary human BM-MSC-derived cells was measured using flow cytometry analysis. Data are presented as mean ± SD (n ¼ 3). (D) acLDL-uptake assay. BM-MSCs, BM-MSC-derived cells, and HUVECs were cultured in a medium containing Alexa Fluor 488-conjugated acLDL to measure their ability to take up acLDL. Scale bar ¼ 20 mm. (E) HA- uptake assay. Primary human BM-MSCs and primary human BM-MSC-derived cells were cultured in a medium containing fluoresceinamine-conjugated HA to measure their ability to take up HA. Scale bar ¼ 20 mm. Abbreviation: LDL, low-density lipoprotein; HA, hyaluronic acid.

    Article Snippet: Primary human bone marrow-derived MSCs (C-12974; PromoCell) were cultured in Mesenchymal Stem Cell Growth Medium 2 (C-28009; PromoCell).

    Techniques: Gene Expression, Derivative Assay, Expressing, Two Tailed Test, Cytometry, Cell Culture