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PromoCell placenta hpc pl cells
Placenta Hpc Pl Cells, supplied by PromoCell, used in various techniques. Bioz Stars score: 95/100, based on 96 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/placenta+hpc+pl/hPC-PL-c+Human+Pericytes/pmc12598698-252-33-44
Average 95 stars, based on 96 article reviews

placenta hpc pl cells - by Bioz Stars, 2026-10

95/100 stars

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Article Title: In vitro evaluation of simulated stereotactic radiotherapy for wet age-related macular degeneration on three different cell lines
Article Snippet: .. Human umbilical vein endothelial cells (HUVEC) and human pericytes from placenta (hPC-PL) were obtained as primary, proliferating, freshly isolated cells (PromoCell, Heidelberg, Germany). .. Either pericyte growth medium or endothelial cell growth medium with supplement growth factor mix and 2% FCS (PromoCell) were used.

Cell Culture:

Article Title: Adult Human Multipotent Neural Cells Could Be Distinguished from Other Cell Types by Proangiogenic Paracrine Effects via MCP-1 and GRO.
Article Snippet: We followed the methods of Lee et al. [22]; fNSCs were purchased from Millipore (Billerica, MA, USA) and maintained in ReNcell maintenance medium (Millipore) supplemented with 20 ng/ml human epidermal growth factor (EGF) (R&D Systems; Minneapolis, MN, USA), 20 ng/ml human basic fibroblast growth factor (bFGF) (R&D Systems), and 100U/ml penicillin/streptomycin (P/S) (Corning Inc.; NY, USA). .. Human pericytes from placenta (hPC-PL) and human umbilical vein endothelial cells (HUVECs) were purchased from PromoCell (Heidelberg, Germany) and cultured in pericyte growth medium (PGM) (PromoCell) and endothelial growth medium (EGM) (PromoCell), respectively. ..

Article Title: p53 rapidly restructures 3D chromatin organization to trigger a transcriptional response.
Article Snippet: Human Umbilical Vein Endothelial Cells (HUVEC) (Lonza, C2519A) and Human Dermal Lymphatic Endothelial Nature Communications | (2024) 15:2821 12 Cells (HDLEC) (Promocell, C-12217) were cultured in 0.5% gelatine‐ coated culture well in EGM2 medium (PromoCell, C-22211) supplemented with Endothelial Cell Growth Medium 2 KIT (Promocell, C-22111), 10% FBS (Gibco, 10270-106), 1% penicillin/streptomycin (Gibco, 15140-122). .. Human Pericytes from Placenta (hPC-PL) (Promocell, C-12980) were cultured in Perycte growth media (Promocell, C-28041) with supplement mix, 10%FBS (Gibco, 10270-106), 1% penicillin/streptomycin (Gibco, 15140-122). ..

Article Title: p53 rapidly restructures 3D chromatin organization to trigger a transcriptional response
Article Snippet: Human Umbilical Vein Endothelial Cells (HUVEC) (Lonza, C2519A) and Human Dermal Lymphatic Endothelial Cells (HDLEC) (Promocell, C-12217) were cultured in 0.5% gelatine‐coated culture well in EGM2 medium (PromoCell, C-22211) supplemented with Endothelial Cell Growth Medium 2 KIT (Promocell, C-22111), 10% FBS (Gibco, 10270-106), 1% penicillin/streptomycin (Gibco, 15140-122). .. Human Pericytes from Placenta (hPC-PL) (Promocell, C-12980) were cultured in Perycte growth media (Promocell, C-28041) with supplement mix, 10%FBS (Gibco, 10270-106), 1% penicillin/streptomycin (Gibco, 15140-122). ..

Article Title: Attenuation of Flightless I Increases Human Pericyte Proliferation, Migration and Angiogenic Functions and Improves Healing in Murine Diabetic Wounds
Article Snippet: .. Human pericytes from placenta (hPC-PL) were purchased and cultured in Human Pericyte Media as per company instructions (Promocell, Heidelberg, Germany). .. Transfection of siFlii (GCUGGAACACUUGUCUGUGdTdT, CACAGACAAGUGUUCCAGCdTdT) or siControl (GGUUAGCCGCACGUUAGUUdTdT, AACUAACGUGCGGCUAACCdTdT) constructs (Sigma-Aldrich, Darmstadt, Germany) was carried out in suspension using Lipofectamine 2000 (ThermoFisher Scientific, Waltham, MA, USA), as described previously [ ].

Article Title: Adult Human Multipotent Neural Cells Could Be Distinguished from Other Cell Types by Proangiogenic Paracrine Effects via MCP-1 and GRO
Article Snippet: We followed the methods of Lee et al. [ ]; fNSCs were purchased from Millipore (Billerica, MA, USA) and maintained in ReNcell maintenance medium (Millipore) supplemented with 20 ng/ml human epidermal growth factor (EGF) (R&D Systems; Minneapolis, MN, USA), 20 ng/ml human basic fibroblast growth factor (bFGF) (R&D Systems), and 100 U/ml penicillin/streptomycin (P/S) (Corning Inc.; NY, USA). .. Human pericytes from placenta (hPC-PL) and human umbilical vein endothelial cells (HUVECs) were purchased from PromoCell (Heidelberg, Germany) and cultured in pericyte growth medium (PGM) (PromoCell) and endothelial growth medium (EGM) (PromoCell), respectively. ..

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Fig. 3 Effects of pericytes on vascular and total permeability of placental barrier model on days 16 and 18 of culture. A. Brightfield images of vascular channel for the following conditions: no cell control, ST only, ST + HUVECs, and two tricultures with ST + HUVECs + hPC-PLs at high and low density. Fluorescent images of 4 kDa (green) and 65 kDa (red) dextran permeation through the endothelial channel after 1 hour of perfusion. B. Vascular barrier permeability to 4 kDa dextran. (N = 3–7, one-way ANOVA, *p < 0.05, **p < 0.01, ***p < 0.001) C. Vascular barrier permeability to 65 kDa dextran. (N = 3–7, one-way ANOVA, *p < 0.05, **p < 0.01, ***p < 0.001) D. Fluorescent images of 65 kDa dextran (red) permeating from the central maternal compartment, through the ST and HUVEC barriers, to the adjacent fetal compartments after 24 hours. E. Total barrier permeability to 4 kDa dextran from the maternal to the fetal compartments. (N = 6–7, one-way ANOVA, **p < 0.01, ***p < 0.001) F. Total barrier permeability to 65 kDa dextran from the maternal to the fetal compartments. (N = 6–7, one-way ANOVA, ***p < 0.001).

Journal: Lab on a chip

Article Title: Late-stage placental barrier model for transport studies of prescription drugs during pregnancy.

doi: 10.1039/d5lc00075k

Figure Lengend Snippet: Fig. 3 Effects of pericytes on vascular and total permeability of placental barrier model on days 16 and 18 of culture. A. Brightfield images of vascular channel for the following conditions: no cell control, ST only, ST + HUVECs, and two tricultures with ST + HUVECs + hPC-PLs at high and low density. Fluorescent images of 4 kDa (green) and 65 kDa (red) dextran permeation through the endothelial channel after 1 hour of perfusion. B. Vascular barrier permeability to 4 kDa dextran. (N = 3–7, one-way ANOVA, *p < 0.05, **p < 0.01, ***p < 0.001) C. Vascular barrier permeability to 65 kDa dextran. (N = 3–7, one-way ANOVA, *p < 0.05, **p < 0.01, ***p < 0.001) D. Fluorescent images of 65 kDa dextran (red) permeating from the central maternal compartment, through the ST and HUVEC barriers, to the adjacent fetal compartments after 24 hours. E. Total barrier permeability to 4 kDa dextran from the maternal to the fetal compartments. (N = 6–7, one-way ANOVA, **p < 0.01, ***p < 0.001) F. Total barrier permeability to 65 kDa dextran from the maternal to the fetal compartments. (N = 6–7, one-way ANOVA, ***p < 0.001).

Article Snippet: Primary human placental pericytes (hPC-PL) were obtained from PromoCell (C-12980), cultured in pericyte growth medium 2 (PGM2, Millipore Sigma, C-28041) and used until passage 5.

Techniques: Permeability, Control

STAT3 expression is reduced in HFpEF pericytes. (A, B) Immunofluorescence staining of control (Ctrl) and HFpEF patient biopsy. (A) Measurement of capillary perimeter. (B) Quantification of pericyte coverage normalised to the vasculature. N = 4 for control and N = 7 for HFpEF. Every data point represents one independent patient. Data are shown as mean ± SEM. P values were calculated using unpaired, two‐tailed Student's t ‐test. (C) Immunofluorescence staining of control and HFpEF mice. Quantification of pericyte coverage normalised to the vasculature. Pericytes were labelled with NG2. N = 4 for control and N = 4 for HFpEF. Every data point represents one independent mouse. Data are shown as mean ± SEM. P value was calculated using unpaired, two‐tailed Student's t ‐test. (D) Uniform Manifold Approximation and Projection (UMAP) plot showing cell‐type specific clustering of all data points from cardiac single‐nuclei sequencing. we identified 13 individual cell types: Cardiomyocytes (CM), Artery (ArtEC), Vein (VeinEC), Capillary (CapEC) and Lymphatic (LymphEC) Endothelial Cells, B Cells, Macrophages (MP), Adipocytes (Adip), Fibroblasts (FB), Pericytes (PC), Smooth Muscle Cells (SMC), Meothelial cells (Meso), Neuronal cells (NC). (E) Gene Ontology (GO) enrichment analysis of significant differentially expressed genes in HFpEF pericytes. Represented are the top 10 downregulated cellular compartments and biological processes. (F) Scatter plot showing Stat3 normalised gene expression values (unique molecular identifier, UMI) for the pericyte cluster in control and HFpEF pericytes. N = 9 for control and N = 3 for HFpEF. Every data point represents one independent mouse. Data are shown as mean ± SEM. P value was calculated using bimod test. (G) Scatter plot showing Stat3 normalised gene expression values (fragments per kilobase of transcript per million mapped reads, FPKM) in control and HFpEF hearts. N = 24 for control and N = 41 for HFpEF. Every data point represents one independent patient. Data are shown as mean ± SEM. P value was calculated using Mann–Whitney test. (H) Immunofluorescence staining of control and HFpEF mice. STAT3 protein expression is reduced in HFpEF mice. N = 4 for control and N = 4 for HFpEF. Every data point represents one independent mouse. Data are shown as mean ± SEM. P value was calculated using unpaired, two‐tailed Student's t ‐test.

Journal: Febs Letters

Article Title: STAT3 expression is reduced in cardiac pericytes in HFpEF and its loss reduces cellular adhesion and induces pericyte senescence

doi: 10.1002/1873-3468.70057

Figure Lengend Snippet: STAT3 expression is reduced in HFpEF pericytes. (A, B) Immunofluorescence staining of control (Ctrl) and HFpEF patient biopsy. (A) Measurement of capillary perimeter. (B) Quantification of pericyte coverage normalised to the vasculature. N = 4 for control and N = 7 for HFpEF. Every data point represents one independent patient. Data are shown as mean ± SEM. P values were calculated using unpaired, two‐tailed Student's t ‐test. (C) Immunofluorescence staining of control and HFpEF mice. Quantification of pericyte coverage normalised to the vasculature. Pericytes were labelled with NG2. N = 4 for control and N = 4 for HFpEF. Every data point represents one independent mouse. Data are shown as mean ± SEM. P value was calculated using unpaired, two‐tailed Student's t ‐test. (D) Uniform Manifold Approximation and Projection (UMAP) plot showing cell‐type specific clustering of all data points from cardiac single‐nuclei sequencing. we identified 13 individual cell types: Cardiomyocytes (CM), Artery (ArtEC), Vein (VeinEC), Capillary (CapEC) and Lymphatic (LymphEC) Endothelial Cells, B Cells, Macrophages (MP), Adipocytes (Adip), Fibroblasts (FB), Pericytes (PC), Smooth Muscle Cells (SMC), Meothelial cells (Meso), Neuronal cells (NC). (E) Gene Ontology (GO) enrichment analysis of significant differentially expressed genes in HFpEF pericytes. Represented are the top 10 downregulated cellular compartments and biological processes. (F) Scatter plot showing Stat3 normalised gene expression values (unique molecular identifier, UMI) for the pericyte cluster in control and HFpEF pericytes. N = 9 for control and N = 3 for HFpEF. Every data point represents one independent mouse. Data are shown as mean ± SEM. P value was calculated using bimod test. (G) Scatter plot showing Stat3 normalised gene expression values (fragments per kilobase of transcript per million mapped reads, FPKM) in control and HFpEF hearts. N = 24 for control and N = 41 for HFpEF. Every data point represents one independent patient. Data are shown as mean ± SEM. P value was calculated using Mann–Whitney test. (H) Immunofluorescence staining of control and HFpEF mice. STAT3 protein expression is reduced in HFpEF mice. N = 4 for control and N = 4 for HFpEF. Every data point represents one independent mouse. Data are shown as mean ± SEM. P value was calculated using unpaired, two‐tailed Student's t ‐test.

Article Snippet: Human placenta pericytes (hPL‐PC, C‐12980, PromoCell, Heidelberg, Germany) were cultured in Pericyte Growth Medium 2 (C‐28041, PromoCell) at 37 °C and 5% CO 2 .

Techniques: Expressing, Immunofluorescence, Staining, Control, Two Tailed Test, Sequencing, Gene Expression, MANN-WHITNEY

STAT3 deficiency compromises pericytes adhesion. (A) Scheme of the experimental design and RT‐qPCR gene expression analysis of STAT3 showing efficient STAT3 silencing in pericytes. Every data point ( n = 6) represents an independent transfection. Data are shown as mean ± SEM. P values were calculated using unpaired, two‐tailed Student's t ‐test. (B) RT‐qPCR gene expression analysis of PDGFRB and CSPG4 . Every data point ( n = 6) represents an independent transfection. Data are shown as mean ± SEM. P values were calculated using unpaired, two‐tailed Student's t ‐test. (C) Immunofluorescence staining of control and STAT3‐deficient pericytes. Every data point ( n = 6) represents an independent transfection. Data are shown as mean ± SEM. P values were calculated using unpaired, two‐tailed Student's t ‐test. (D) RT‐qPCR gene expression analysis of COL1A1 and COL3A1 . Every data point ( n = 6) represents an independent transfection. Data are shown as mean ± SEM. P values were calculated using unpaired, two‐tailed Student's t ‐test. (E) Immunofluorescence staining of control and STAT3‐deficient pericytes. Violin plots representing every analysed cell in a total of N = 6 independent transfections. P values were calculated using unpaired, Mann–Whitney test. (F) RT‐qPCR gene expression analysis of DES . Every data point ( n = 6) represents an independent transfection. Data are shown as mean ± SEM. P values were calculated using unpaired, two‐tailed Student's t ‐test. (G) Adhesion capacity of control and STAT3‐deficient pericytes. Every data point ( n = 9) represents an independent transfection. Data are shown as mean ± SEM. P values were calculated using unpaired, two‐tailed Student's t ‐test.

Journal: Febs Letters

Article Title: STAT3 expression is reduced in cardiac pericytes in HFpEF and its loss reduces cellular adhesion and induces pericyte senescence

doi: 10.1002/1873-3468.70057

Figure Lengend Snippet: STAT3 deficiency compromises pericytes adhesion. (A) Scheme of the experimental design and RT‐qPCR gene expression analysis of STAT3 showing efficient STAT3 silencing in pericytes. Every data point ( n = 6) represents an independent transfection. Data are shown as mean ± SEM. P values were calculated using unpaired, two‐tailed Student's t ‐test. (B) RT‐qPCR gene expression analysis of PDGFRB and CSPG4 . Every data point ( n = 6) represents an independent transfection. Data are shown as mean ± SEM. P values were calculated using unpaired, two‐tailed Student's t ‐test. (C) Immunofluorescence staining of control and STAT3‐deficient pericytes. Every data point ( n = 6) represents an independent transfection. Data are shown as mean ± SEM. P values were calculated using unpaired, two‐tailed Student's t ‐test. (D) RT‐qPCR gene expression analysis of COL1A1 and COL3A1 . Every data point ( n = 6) represents an independent transfection. Data are shown as mean ± SEM. P values were calculated using unpaired, two‐tailed Student's t ‐test. (E) Immunofluorescence staining of control and STAT3‐deficient pericytes. Violin plots representing every analysed cell in a total of N = 6 independent transfections. P values were calculated using unpaired, Mann–Whitney test. (F) RT‐qPCR gene expression analysis of DES . Every data point ( n = 6) represents an independent transfection. Data are shown as mean ± SEM. P values were calculated using unpaired, two‐tailed Student's t ‐test. (G) Adhesion capacity of control and STAT3‐deficient pericytes. Every data point ( n = 9) represents an independent transfection. Data are shown as mean ± SEM. P values were calculated using unpaired, two‐tailed Student's t ‐test.

Article Snippet: Human placenta pericytes (hPL‐PC, C‐12980, PromoCell, Heidelberg, Germany) were cultured in Pericyte Growth Medium 2 (C‐28041, PromoCell) at 37 °C and 5% CO 2 .

Techniques: Quantitative RT-PCR, Gene Expression, Transfection, Two Tailed Test, Immunofluorescence, Staining, Control, MANN-WHITNEY

STAT3 deficiency induces cellular senescence in pericytes. (A) Representative FACS plots showing the gating strategy for BrdU proliferation assay. Cell cycle phases distribution differences in control and STAT3‐deficient pericytes. (B) RT‐qPCR gene expression analysis of CDKN1A and TP53 . (C) Measurement of dehydrogenase activity in pericytes using CCK‐8. (D) RT‐qPCR analysis of relative telomere length in control and STAT3‐deficient pericytes. (E) β‐Galactosidase staining of control and STAT3‐deprived pericytes and quantification of β‐galactosidase+ area (%). (A–E) Every data point ( n = 6) represents an independent transfection. Data are shown as mean ± SEM. P values were calculated using unpaired, two‐tailed Student's t ‐test.

Journal: Febs Letters

Article Title: STAT3 expression is reduced in cardiac pericytes in HFpEF and its loss reduces cellular adhesion and induces pericyte senescence

doi: 10.1002/1873-3468.70057

Figure Lengend Snippet: STAT3 deficiency induces cellular senescence in pericytes. (A) Representative FACS plots showing the gating strategy for BrdU proliferation assay. Cell cycle phases distribution differences in control and STAT3‐deficient pericytes. (B) RT‐qPCR gene expression analysis of CDKN1A and TP53 . (C) Measurement of dehydrogenase activity in pericytes using CCK‐8. (D) RT‐qPCR analysis of relative telomere length in control and STAT3‐deficient pericytes. (E) β‐Galactosidase staining of control and STAT3‐deprived pericytes and quantification of β‐galactosidase+ area (%). (A–E) Every data point ( n = 6) represents an independent transfection. Data are shown as mean ± SEM. P values were calculated using unpaired, two‐tailed Student's t ‐test.

Article Snippet: Human placenta pericytes (hPL‐PC, C‐12980, PromoCell, Heidelberg, Germany) were cultured in Pericyte Growth Medium 2 (C‐28041, PromoCell) at 37 °C and 5% CO 2 .

Techniques: Proliferation Assay, Control, Quantitative RT-PCR, Gene Expression, Activity Assay, CCK-8 Assay, Staining, Transfection, Two Tailed Test

STAT3 knockdown induces a transcriptional signature similar to HFpEF. (A) Gene Ontology (GO) enrichment analysis of significant differentially expressed genes in STAT3‐deficient pericytes. Represented are the top 6 dysregulated pathways. (B) Scatter plot showing CDKN1A , CDKN1B and CDKN2B normalised gene expression values (fragments per kilobase of transcript per million mapped reads, FPKM) in control and STAT3‐deficient pericytes hearts. Every data point ( n = 3) represents an independent transfection. Data are shown as mean ± SEM. P values were calculated using cuffdiff test. (C) Gene Ontology (GO) enrichment analysis of significant differentially expressed genes in STAT3‐deficient pericytes. Represented are the top six dysregulated cellular components. (D) Scatter plot showing ARPC5L , RAB21 and GJA1 normalised gene expression values (fragments per kilobase of transcript per million mapped reads, FPKM) in control and STAT3‐deficient pericytes hearts. Every data point ( n = 3) represents an independent transfection. Data are shown as mean ± SEM. P values were calculated using the Wald test for significance of the negative binomial model coefficients, as implemented in DESeq2. (E) Cumulative distribution of the expression change of genes grouped by their total number of STAT3 binding sites in their enhancers. The numbers in parentheses indicate the number of genes in each set. (F) Scatter plot showing COL5A2, COL5A3 and COL27A1 normalised gene expression values (fragments per kilobase of transcript per million mapped reads, FPKM) in control and STAT3‐deficient pericytes hearts. Every data point ( n = 3) represents an independent transfection. Data are shown as mean ± SEM. P values were calculated using the Wald test for significance of the negative binomial model coefficients, as implemented in DESeq2. (G) RT‐qPCR gene expression analysis of STAT3, ACTA2, COL1A1 and COL3A1 in pericytes upon IL‐1β treatment. Every data point ( n = 6) represents an independent transfection. Data are shown as mean ± SEM. P values were calculated using unpaired, two‐tailed Student's t ‐test.

Journal: Febs Letters

Article Title: STAT3 expression is reduced in cardiac pericytes in HFpEF and its loss reduces cellular adhesion and induces pericyte senescence

doi: 10.1002/1873-3468.70057

Figure Lengend Snippet: STAT3 knockdown induces a transcriptional signature similar to HFpEF. (A) Gene Ontology (GO) enrichment analysis of significant differentially expressed genes in STAT3‐deficient pericytes. Represented are the top 6 dysregulated pathways. (B) Scatter plot showing CDKN1A , CDKN1B and CDKN2B normalised gene expression values (fragments per kilobase of transcript per million mapped reads, FPKM) in control and STAT3‐deficient pericytes hearts. Every data point ( n = 3) represents an independent transfection. Data are shown as mean ± SEM. P values were calculated using cuffdiff test. (C) Gene Ontology (GO) enrichment analysis of significant differentially expressed genes in STAT3‐deficient pericytes. Represented are the top six dysregulated cellular components. (D) Scatter plot showing ARPC5L , RAB21 and GJA1 normalised gene expression values (fragments per kilobase of transcript per million mapped reads, FPKM) in control and STAT3‐deficient pericytes hearts. Every data point ( n = 3) represents an independent transfection. Data are shown as mean ± SEM. P values were calculated using the Wald test for significance of the negative binomial model coefficients, as implemented in DESeq2. (E) Cumulative distribution of the expression change of genes grouped by their total number of STAT3 binding sites in their enhancers. The numbers in parentheses indicate the number of genes in each set. (F) Scatter plot showing COL5A2, COL5A3 and COL27A1 normalised gene expression values (fragments per kilobase of transcript per million mapped reads, FPKM) in control and STAT3‐deficient pericytes hearts. Every data point ( n = 3) represents an independent transfection. Data are shown as mean ± SEM. P values were calculated using the Wald test for significance of the negative binomial model coefficients, as implemented in DESeq2. (G) RT‐qPCR gene expression analysis of STAT3, ACTA2, COL1A1 and COL3A1 in pericytes upon IL‐1β treatment. Every data point ( n = 6) represents an independent transfection. Data are shown as mean ± SEM. P values were calculated using unpaired, two‐tailed Student's t ‐test.

Article Snippet: Human placenta pericytes (hPL‐PC, C‐12980, PromoCell, Heidelberg, Germany) were cultured in Pericyte Growth Medium 2 (C‐28041, PromoCell) at 37 °C and 5% CO 2 .

Techniques: Knockdown, Gene Expression, Control, Transfection, Expressing, Binding Assay, Quantitative RT-PCR, Two Tailed Test

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