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PromoCell cell growth medium mv2
Cell Growth Medium Mv2, supplied by PromoCell, used in various techniques. Bioz Stars score: 97/100, based on 523 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/growth+medium+mv2/Endothelial+Cell+Growth+Medium+MV2/pm42243530-70-6-13
Average 97 stars, based on 523 article reviews

cell growth medium mv2 - by Bioz Stars, 2026-10

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Article Title: Endothelial Features Along the Pulmonary Vascular Tree in Chronic Thromboembolic Pulmonary Hypertension: Distinctive or Shared Facets?
Article Snippet: Cells were seeded onto gelatine‐coated flasks (2 mg/mL; Sigma‐Aldrich) in endothelial growth medium MV2 (PromoCell) supplemented with 100 U.mL −1 penicillin, 100 μg.mL −1 streptomycin and 1.25 μg.mL −1 amphotericin B (Life Technologies) and maintained in culture at 37°C, 5% CO 2 and 95% humidity.

Article Title: Endothelial Features Along the Pulmonary Vascular Tree in Chronic Thromboembolic Pulmonary Hypertension: Distinctive or Shared Facets?
Article Snippet: A piece from the large (upstream pulmonary vascular occlusion) and (sub)‐segmental (downstream pulmonary vascular occlusion) pulmonary arteries, free of thrombotic material, was collected separately in endothelial growth medium MV2 (PromoCell) supplemented with 100 U. mL −1 penicillin, 100 μg. ml −1 100 μg. mL −1 streptomycin and 1.25 μg. mL −1 amphotericin B (Life Technologies).

Article Title: Paracrine role of endothelial IGF-1 receptor in depot-specific adipose tissue adaptation in male mice
Article Snippet: Cells were re-suspended in 2 ml supplemented endothelial growth medium–MV2 (PromoCell) and seeded on a 6 well fibronectin coated plates.

Article Title: Paracrine role of endothelial IGF-1 receptor in depot-specific adipose tissue adaptation in male mice.
Article Snippet: Cells were re-suspended in 2ml supplemented endothelial growth medium–MV2 (PromoCell) and seeded on a 6 well fibronectin coated plates.

Cell Culture:

Article Title: Selective EPAC1 activators enhance endothelial function in models of vascular inflammation.
Article Snippet: .. Human coronary artery endothelial cells (HCAECs, PromoCell, C-12221) and human vascular smooth muscle cells (VSMCs, PromoCell, C-12511) were cultured in endothelial growth medium MV2 (PromoCell, C-39226) and smooth muscle growth medium 2 (PromoCell, C-39267), respectively. .. The three-cell culture system was established by first seeding VSMCs onto the basal side of an inverted 0.4 μm pore transwell insert (Corning CLS3450–24EA) at a density of 1.8 × 105 cells per insert.

Article Title: Immunophenotypical Characterization of Limbal Mesenchymal Stromal Cell Subsets during In Vitro Expansion
Article Snippet: However, dermal fibroblast cells (GM08680) were cultured in MEM alpha (Gibco, Taastrup, Denmark) supplemented by 10% FCS (Gibco, Taastrup, Denmark) and 1% Penicillin/Streptomycin (Gibco, Taastrup, Denmark). .. Endothelial cells were cultured in the growth medium MV2 (Promo Cell, Germany) with its specific supplement. ..

Article Title: Immunophenotypical Characterization of Limbal Mesenchymal Stromal Cell Subsets during In Vitro Expansion.
Article Snippet: However, dermal fibroblast cells (GM08680) were cultured in MEM alpha (Gibco, Taastrup, Denmark) supplemented by 10% FCS (Gibco, Taastrup, Denmark) and 1% Penicillin/Streptomycin (Gibco, Taastrup, Denmark). .. Endothelial cells were cultured in the growth medium MV2 (Promo Cell, Germany) with its specific supplement. ..

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Article Title: Inter- and Intra-donor variability in bone marrow-derived mesenchymal stromal cells: implications for clinical applications.
Article Snippet: Background aims: Mesenchymal stromal cells (MSCs) are attractive as a therapeutic modality in multiple disease conditions characterized by inflammation and vascular compromise.. Logistically they are advantageous because they can be isolated from adult tissue sources, such as bonemarrow (BM).. The phase 2a START clinical trial determined BM-MSCs to be safe in patients with moderate-to-severe acute respiratory distress syndrome (ARDS).

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Initially D-VLC-AMC plasmin fluorescent substrate assays were conducted to identify a culture media that does not contain plasminogen system components, so that the effect of plasmin on hCMEC/D3 could be assessed in isolation. The standard EBM-2MV serum containing media for hCMEC/D3, contains plasmin, plasminogen and factors that inhibit plasmin activity, and hence cannot be used for this study (A). serum-free EBM and EBM + 2MV supplements do not contain plasmin, plasminogen or factors that inhibit plasmin activity (A); however, they do contain an insufficient level of protein (Sup Fig 2), which is not physiologically representative and furthermore is unlikely to support low quantities of plasmin protein in solution. The base media was therefore changed to AIM-V, which contains a higher level of protein. AIM-V + 2MV supplements does not contain plasmin or plasminogen, and does not inhibit plasmin activity, and hence is suitable for studying the direct effect of exogenous plasmin on hCMEC/D3 (C). The data presented are the mean ± SEM of three independent experiments. ECIS monitoring demonstrates that AIM-V-2MV serum-free media supports the maintenance of a stable functional hCMEC/D3 brain endothelial barrier, with similar properties to hCMEC/D3 layers cultured in EBM-2MV serum-free media (B, C, E, & F). Briefly hCMEC/D3 cells were seeded into ECIS 96W20IDF plates and cultured in EBM-2MV serum containing media for 48 hours to allow a stable barrier to form. Cells were then washed thrice with their respective future culture media (i.e. AIM-V-2MV serum-free media, EBM-2MV serum-free media or EBM-2MV serum containing media). Cells were then cultured in their respective media for a further 40 hours. Barrier properties were monitored in real-time throughout the experiment using ECIS. Ribbon plots represent the mean ± SEM of data from three independent experiments, each consisting of three technical replicates. Data was normalised before treatments were applied using vascr. Immunocytochemistry illustrates that hCMEC/D3 brain endothelial cells cultured in AIM-V-2MV serum-free media express the key junction associated molecules VE-cadherin (CD144), p -Catenin, Claudin-5, ZO-1 and PECAM-1 (CD31) (D). Briefly hCMEC/D3 cells were cultured in Ibidi 96 well plates in EBM-2MV serum containing media for 48 hours. Cells were then washed thrice with their respective future culture media (i.e. AIM-V-2MV serum-free media or EBM-2MV serum containing media) and cultured in their respective media for 16 hours. Cells were fixed with paraformaldehyde, probed with antibodies detecting junctional molecules, washed, and probed with respective fluorophore conjugated secondary antibodies and DAPI. Cells were imaged using an Operetta CLS. Images are representative of 9 fields from each of three independent experiments.

Journal: bioRxiv

Article Title: Plasmin, the product of tissue plasminogen activator (tPA) treatment for ischemic stroke, impairs human brain endothelial barrier integrity

doi: 10.64898/2026.05.27.728289

Figure Lengend Snippet: Initially D-VLC-AMC plasmin fluorescent substrate assays were conducted to identify a culture media that does not contain plasminogen system components, so that the effect of plasmin on hCMEC/D3 could be assessed in isolation. The standard EBM-2MV serum containing media for hCMEC/D3, contains plasmin, plasminogen and factors that inhibit plasmin activity, and hence cannot be used for this study (A). serum-free EBM and EBM + 2MV supplements do not contain plasmin, plasminogen or factors that inhibit plasmin activity (A); however, they do contain an insufficient level of protein (Sup Fig 2), which is not physiologically representative and furthermore is unlikely to support low quantities of plasmin protein in solution. The base media was therefore changed to AIM-V, which contains a higher level of protein. AIM-V + 2MV supplements does not contain plasmin or plasminogen, and does not inhibit plasmin activity, and hence is suitable for studying the direct effect of exogenous plasmin on hCMEC/D3 (C). The data presented are the mean ± SEM of three independent experiments. ECIS monitoring demonstrates that AIM-V-2MV serum-free media supports the maintenance of a stable functional hCMEC/D3 brain endothelial barrier, with similar properties to hCMEC/D3 layers cultured in EBM-2MV serum-free media (B, C, E, & F). Briefly hCMEC/D3 cells were seeded into ECIS 96W20IDF plates and cultured in EBM-2MV serum containing media for 48 hours to allow a stable barrier to form. Cells were then washed thrice with their respective future culture media (i.e. AIM-V-2MV serum-free media, EBM-2MV serum-free media or EBM-2MV serum containing media). Cells were then cultured in their respective media for a further 40 hours. Barrier properties were monitored in real-time throughout the experiment using ECIS. Ribbon plots represent the mean ± SEM of data from three independent experiments, each consisting of three technical replicates. Data was normalised before treatments were applied using vascr. Immunocytochemistry illustrates that hCMEC/D3 brain endothelial cells cultured in AIM-V-2MV serum-free media express the key junction associated molecules VE-cadherin (CD144), p -Catenin, Claudin-5, ZO-1 and PECAM-1 (CD31) (D). Briefly hCMEC/D3 cells were cultured in Ibidi 96 well plates in EBM-2MV serum containing media for 48 hours. Cells were then washed thrice with their respective future culture media (i.e. AIM-V-2MV serum-free media or EBM-2MV serum containing media) and cultured in their respective media for 16 hours. Cells were fixed with paraformaldehyde, probed with antibodies detecting junctional molecules, washed, and probed with respective fluorophore conjugated secondary antibodies and DAPI. Cells were imaged using an Operetta CLS. Images are representative of 9 fields from each of three independent experiments.

Article Snippet: AIM-V serum-free media was prepared by supplementing AIM-V media (ThermoFisher Scientific, 12055091) with 1X GlutaMAX (ThermoFisher Scientific, 35050061) and 2MV supplements (PromoCell, C-39221 with FCS omitted) and stored at −80°C.

Techniques: Isolation, Activity Assay, Functional Assay, Cell Culture, Immunocytochemistry

hCMEC/D3 cells were seeded into ECIS 96W20IDF plates and cultured in EBM-2MV serum containing media for 48 hours to allow a stable barrier to form. Cells were then washed thrice with AIM-V-2MV serum-free media and cultured for 16 hours in AIM-V-2MV serum-free media. Cells were washed thrice and cultured for 1 hour in fresh AIM-V-2MV serum-free media ± 640nM plasminogen. tPA was then added to the respective wells and cells cultured for a further 24 hours. Barrier properties were monitored in real-time throughout the experiment using ECIS. Ribbon plots represent the mean ± SEM of data from three independent experiments, each consisting of three technical replicates. Data was normalised 1hr before plasminogen was added, using vascr. Statistical analysis of this data was carried out at 4 and 12 hours after tPA addition; each treatment response was compared with vehicle control using two-way ANOVA with Dunnett’s test (* p <0.05, ** p <0.01).

Journal: bioRxiv

Article Title: Plasmin, the product of tissue plasminogen activator (tPA) treatment for ischemic stroke, impairs human brain endothelial barrier integrity

doi: 10.64898/2026.05.27.728289

Figure Lengend Snippet: hCMEC/D3 cells were seeded into ECIS 96W20IDF plates and cultured in EBM-2MV serum containing media for 48 hours to allow a stable barrier to form. Cells were then washed thrice with AIM-V-2MV serum-free media and cultured for 16 hours in AIM-V-2MV serum-free media. Cells were washed thrice and cultured for 1 hour in fresh AIM-V-2MV serum-free media ± 640nM plasminogen. tPA was then added to the respective wells and cells cultured for a further 24 hours. Barrier properties were monitored in real-time throughout the experiment using ECIS. Ribbon plots represent the mean ± SEM of data from three independent experiments, each consisting of three technical replicates. Data was normalised 1hr before plasminogen was added, using vascr. Statistical analysis of this data was carried out at 4 and 12 hours after tPA addition; each treatment response was compared with vehicle control using two-way ANOVA with Dunnett’s test (* p <0.05, ** p <0.01).

Techniques: Cell Culture, Control

Journal: bioRxiv

Article Title: Plasmin, the product of tissue plasminogen activator (tPA) treatment for ischemic stroke, impairs human brain endothelial barrier integrity

doi: 10.64898/2026.05.27.728289

Figure Lengend Snippet: hCMEC/D3 cells were seeded into ECIS 96W20IDF plates and cultured in EBM-2MV serum containing media for 48 hours to allow a stable barrier to form. Cells were then washed thrice with AIM-V-2MV serum-free media and cultured in this media for 16 hours. Media was removed and replaced with respective treatment in AIM-V-2MV serum-free media. Cells were cultured for 24 hours. Barrier properties were monitored in real-time throughout the experiment using ECIS. Ribbon plots represent the mean ± SEM of data from three independent experiments, each consisting of three technical replicates (A-D). Data were normalised 2 hours before the addition of treatment using vascr. Statistical analysis of this data was carried out at 4 and 12 hours after treatment addition; each treatment response was compared with vehicle control using two-way ANOVA with Dunnett’s test (* p <0.05, ** p<0.01, *** p < 0.001,, **** p < 0.0001) (E-H).

Techniques: Cell Culture, Control

Journal: bioRxiv

Article Title: Plasmin, the product of tissue plasminogen activator (tPA) treatment for ischemic stroke, impairs human brain endothelial barrier integrity

doi: 10.64898/2026.05.27.728289

Figure Lengend Snippet: hCMEC/D3 cells were seeded into ECIS 96W20IDF plates and cultured in EBM-2MV serum containing media for 48 hours to allow a stable barrier to form. Cells were then washed thrice with AIM-V-2MV serum-free media and cultured in this media for 16 hours. Media was removed and replaced with respective treatment in AIM-V-2MV serum-free media. Cells were cultured for 24 hours. Barrier properties were monitored in real-time throughout the experiment using ECIS. Ribbon plots represent the mean ± SEM of data from three independent experiments, each consisting of three technical replicates (A-D). Data was normalised 1 hour before the addition of treatment using vascr. Statistical analysis of this data was carried out at 4 and 12 hours after treatment addition; each treatment response was compared with vehicle control using two-way ANOVA with Dunnett’s test (* p <0.05, *** p < 0.001).

Techniques: Cell Culture, Control

hCMEC/D3 cells were seeded into Ibidi 96 well plates in EBM-2MV serum containing media for 48 hours. Cells were then washed thrice with AIM-V-2MV serum-free media and cultured in AIM-V-2MV serum-free media for 16 hours. Vehicle or 640nM plasmin was then added and cells were cultured for 4 or 12 hours. Cells were fixed with paraformaldehyde, probed with antibodies detecting junctional molecules (VE-cadherin (CD144), β-Catenin, Claudin-5, ZO-1 and PECAM-1 (CD31) ), washed, and detected with their respective fluorophore conjugated secondary antibodies and DAPI. Single planes of the wells were imaged using an Operetta CLS. The images shown are representative of 9 fields from each of three independent experiments (A). Vjunctr was then used to quantify the total fluorescence intensity and the fluorescence intensity in the junctional area for each junctional molecule (B & C). The bar charts represent the mean ± SEM of data from three independent experiments, each of which consisted of three technical replicates of nine randomly selected fields from each well. Significant differences between plasmin and vehicle control for each junctional molecule was analysed using two-way ANOVA with Tukey’s range test (*** p<0.001).

Journal: bioRxiv

Article Title: Plasmin, the product of tissue plasminogen activator (tPA) treatment for ischemic stroke, impairs human brain endothelial barrier integrity

doi: 10.64898/2026.05.27.728289

Figure Lengend Snippet: hCMEC/D3 cells were seeded into Ibidi 96 well plates in EBM-2MV serum containing media for 48 hours. Cells were then washed thrice with AIM-V-2MV serum-free media and cultured in AIM-V-2MV serum-free media for 16 hours. Vehicle or 640nM plasmin was then added and cells were cultured for 4 or 12 hours. Cells were fixed with paraformaldehyde, probed with antibodies detecting junctional molecules (VE-cadherin (CD144), β-Catenin, Claudin-5, ZO-1 and PECAM-1 (CD31) ), washed, and detected with their respective fluorophore conjugated secondary antibodies and DAPI. Single planes of the wells were imaged using an Operetta CLS. The images shown are representative of 9 fields from each of three independent experiments (A). Vjunctr was then used to quantify the total fluorescence intensity and the fluorescence intensity in the junctional area for each junctional molecule (B & C). The bar charts represent the mean ± SEM of data from three independent experiments, each of which consisted of three technical replicates of nine randomly selected fields from each well. Significant differences between plasmin and vehicle control for each junctional molecule was analysed using two-way ANOVA with Tukey’s range test (*** p<0.001).

Techniques: Cell Culture, Fluorescence, Control

Brain pericyte secretions mediate the inhibition of TNBC cell adhesion to the BBB. (A) Experimental workflow for adhesion assay. All BBB experiments were performed using ECGMV2 medium with supplements for all conditions from day −6 to the end of the experiment. The astrocyte medium was renewed 24 h before the adhesion experiment with the same ECGMV2 medium. Endothelial cells (ECs) and brain pericytes (hBPs) were co‐cultured for 5 days, and inserts containing brain‐like endothelial cells (hBLECs) were then either maintained with hBPs or transferred to wells without hBPs. After 24 hours, and prior to MDA‐MB‐231 cells seeding, inserts were subjected to the following conditions: maintained without hBPs (hBLEC 24h); transferred to hBPs previously cultured alone for 24 hours (hBLEC 24h then hBP); transferred to wells without hBPs but containing either culture medium (hBLEC) or CM from co‐culture (hBLEC + CM coc ); transferred to wells with astrocytes (hBLEC + A) or maintained in co‐culture with hBPs (hBLEC + hBP). (B–G), Quantification (B, D, F) of MDA‐MB‐231 cell adhesion to hBLECs after 3 h of incubation and representative images (C, E, G) of adhered MDA‐MB‐231 cells (green) under the different conditions. Data are obtained from three independent experiments, with three technical replicates per condition. Statistical analyses were performed using one‐way ANOVA followed by Tukey's test (B), Welch's ANOVA followed by Dunnett's T3 test (D) and Kruskal–Wallis test followed by Dunn's test (F). CM coc = conditioned medium from 24 h hBLECs and hBPs coculture, A = astrocytes, hBP mono = 24 h hBPs monoculture. Scale bar = 750 µm. BBB, blood–brain barrier; ECGMV2, EC Growth Medium MV 2; ECs, endothelial cells; hBLECs, human brain‐like endothelial cells; ns, non‐significant; hBPs, human brain pericytes; TNBC, triple‐negative breast cancer. **** p ≤ 0.0001; * p ≤ 0.05.

Journal: Journal of Cell Communication and Signaling

Article Title: Human brain pericytes protect the blood–brain barrier from triple‐negative breast cancer cells while promoting tumor aggressiveness

doi: 10.1002/ccs3.70070

Figure Lengend Snippet: Brain pericyte secretions mediate the inhibition of TNBC cell adhesion to the BBB. (A) Experimental workflow for adhesion assay. All BBB experiments were performed using ECGMV2 medium with supplements for all conditions from day −6 to the end of the experiment. The astrocyte medium was renewed 24 h before the adhesion experiment with the same ECGMV2 medium. Endothelial cells (ECs) and brain pericytes (hBPs) were co‐cultured for 5 days, and inserts containing brain‐like endothelial cells (hBLECs) were then either maintained with hBPs or transferred to wells without hBPs. After 24 hours, and prior to MDA‐MB‐231 cells seeding, inserts were subjected to the following conditions: maintained without hBPs (hBLEC 24h); transferred to hBPs previously cultured alone for 24 hours (hBLEC 24h then hBP); transferred to wells without hBPs but containing either culture medium (hBLEC) or CM from co‐culture (hBLEC + CM coc ); transferred to wells with astrocytes (hBLEC + A) or maintained in co‐culture with hBPs (hBLEC + hBP). (B–G), Quantification (B, D, F) of MDA‐MB‐231 cell adhesion to hBLECs after 3 h of incubation and representative images (C, E, G) of adhered MDA‐MB‐231 cells (green) under the different conditions. Data are obtained from three independent experiments, with three technical replicates per condition. Statistical analyses were performed using one‐way ANOVA followed by Tukey's test (B), Welch's ANOVA followed by Dunnett's T3 test (D) and Kruskal–Wallis test followed by Dunn's test (F). CM coc = conditioned medium from 24 h hBLECs and hBPs coculture, A = astrocytes, hBP mono = 24 h hBPs monoculture. Scale bar = 750 µm. BBB, blood–brain barrier; ECGMV2, EC Growth Medium MV 2; ECs, endothelial cells; hBLECs, human brain‐like endothelial cells; ns, non‐significant; hBPs, human brain pericytes; TNBC, triple‐negative breast cancer. **** p ≤ 0.0001; * p ≤ 0.05.

Article Snippet: Differentiated ECs were cultured in 100‐mm Petri dishes (Corning) coated with gelatin (Sigma‐Aldrich), in EC growth medium MV 2 (ECGMV2 + Supplement mix C‐39226, PromoCell) and gentamicin (50 μg/ml; Biowest). hBPs (female) were provided by Dr. Fumitaka Shimizu and Pr.

Techniques: Inhibition, Cell Adhesion Assay, Cell Culture, Co-Culture Assay, Incubation

Brain pericytes limit TNBC cell adhesion to the BBB under hypoxic conditions. (A) Experimental workflow for adhesion assay in hypoxic conditions. All BBB experiments were performed using ECGMV2 medium with supplements for all conditions from day −6 to the end of the experiment. After 5 days of co‐culture with brain pericytes (hBPs), inserts containing brain‐like endothelial cells (hBLECs) were exposed to hypoxia for 24 h in the presence or absence of hBPs. Parallel conditions maintained in normoxia served as controls. (B–E) Quantification (B, D) of MDA‐MB‐231 cell adhesion to hBLECs after 3 h of incubation and representative images (C, E) of adhered MDA‐MB‐231 cells (green) under the different conditions. Data are obtained from three independent experiments, with three technical replicates per condition. Statistical analyses were performed using Welch's ANOVA followed by Dunnett's T3 test (B) and Kruskal‐Wallis test followed by Dunn's test (D). hBP‐CM mono = conditioned medium from 24 h hBPs monoculture. Scale bar = 750 μm. BBB, blood–brain barrier; ECGMV2, EC Growth Medium MV 2; hBLECs, human brain‐like endothelial cells; hBPs, human brain pericytes; ns, non‐significant; TNBC, triple‐negative breast cancer. *** p ≤ 0.001; ** p ≤ 0.01; * p ≤ 0.05.

Journal: Journal of Cell Communication and Signaling

Article Title: Human brain pericytes protect the blood–brain barrier from triple‐negative breast cancer cells while promoting tumor aggressiveness

doi: 10.1002/ccs3.70070

Figure Lengend Snippet: Brain pericytes limit TNBC cell adhesion to the BBB under hypoxic conditions. (A) Experimental workflow for adhesion assay in hypoxic conditions. All BBB experiments were performed using ECGMV2 medium with supplements for all conditions from day −6 to the end of the experiment. After 5 days of co‐culture with brain pericytes (hBPs), inserts containing brain‐like endothelial cells (hBLECs) were exposed to hypoxia for 24 h in the presence or absence of hBPs. Parallel conditions maintained in normoxia served as controls. (B–E) Quantification (B, D) of MDA‐MB‐231 cell adhesion to hBLECs after 3 h of incubation and representative images (C, E) of adhered MDA‐MB‐231 cells (green) under the different conditions. Data are obtained from three independent experiments, with three technical replicates per condition. Statistical analyses were performed using Welch's ANOVA followed by Dunnett's T3 test (B) and Kruskal‐Wallis test followed by Dunn's test (D). hBP‐CM mono = conditioned medium from 24 h hBPs monoculture. Scale bar = 750 μm. BBB, blood–brain barrier; ECGMV2, EC Growth Medium MV 2; hBLECs, human brain‐like endothelial cells; hBPs, human brain pericytes; ns, non‐significant; TNBC, triple‐negative breast cancer. *** p ≤ 0.001; ** p ≤ 0.01; * p ≤ 0.05.

Techniques: Cell Adhesion Assay, Co-Culture Assay, Incubation

Brain pericytes maintain BBB integrity in the presence of TNBC cells under hypoxic conditions and supplement deprivation. (A) After 5 days of co‐culture with brain pericytes (hBPs) in ECGMV2 medium with supplements, inserts containing brain‐like endothelial cells (hBLECs) co‐cultured with hBPs were exposed to hypoxia for 16 h following medium replacement with ECGMV2 basal medium (without supplements). Then, endothelial permeability (Pe) to Lucifer Yellow was assessed after 3 h of incubation with MDA‐MB‐231 cells, in the presence or absence of hBPs, under normoxic and hypoxic conditions. (B) Permeability values (expressed in x10 −3 cm/min ± SD) are summarized in a table. (C) Representative images of endothelial Claudin‐5 (magenta) immunostaining in the absence or presence of hBPs after 3 h of incubation with MDA‐MB‐231 cells (green) under hypoxic conditions in basal medium. Data are obtained from three independent experiments, with three technical replicates per condition. Statistical analyses were performed using Welch's ANOVA followed by Dunnett's T3 test. MDA = MDA‐MB‐231 cells. Scale bars = 300 μm (10X) and 100 μm (40X). BBB, blood–brain barrier; ECGMV2, EC Growth Medium MV 2; hBLECs, human brain‐like endothelial cells; hBPs, human brain pericytes; ns, non‐significant; TNBC, triple‐negative breast cancer. *** p ≤ 0.001; ** p ≤ 0.01; * p ≤ 0.05.

Journal: Journal of Cell Communication and Signaling

Article Title: Human brain pericytes protect the blood–brain barrier from triple‐negative breast cancer cells while promoting tumor aggressiveness

doi: 10.1002/ccs3.70070

Figure Lengend Snippet: Brain pericytes maintain BBB integrity in the presence of TNBC cells under hypoxic conditions and supplement deprivation. (A) After 5 days of co‐culture with brain pericytes (hBPs) in ECGMV2 medium with supplements, inserts containing brain‐like endothelial cells (hBLECs) co‐cultured with hBPs were exposed to hypoxia for 16 h following medium replacement with ECGMV2 basal medium (without supplements). Then, endothelial permeability (Pe) to Lucifer Yellow was assessed after 3 h of incubation with MDA‐MB‐231 cells, in the presence or absence of hBPs, under normoxic and hypoxic conditions. (B) Permeability values (expressed in x10 −3 cm/min ± SD) are summarized in a table. (C) Representative images of endothelial Claudin‐5 (magenta) immunostaining in the absence or presence of hBPs after 3 h of incubation with MDA‐MB‐231 cells (green) under hypoxic conditions in basal medium. Data are obtained from three independent experiments, with three technical replicates per condition. Statistical analyses were performed using Welch's ANOVA followed by Dunnett's T3 test. MDA = MDA‐MB‐231 cells. Scale bars = 300 μm (10X) and 100 μm (40X). BBB, blood–brain barrier; ECGMV2, EC Growth Medium MV 2; hBLECs, human brain‐like endothelial cells; hBPs, human brain pericytes; ns, non‐significant; TNBC, triple‐negative breast cancer. *** p ≤ 0.001; ** p ≤ 0.01; * p ≤ 0.05.

Techniques: Co-Culture Assay, Cell Culture, Permeability, Incubation, Immunostaining

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