4.4 Article

Porcine ovarian cortex-derived putative stem cells can differentiate into endothelial cells in vitro

期刊

HISTOCHEMISTRY AND CELL BIOLOGY
卷 156, 期 4, 页码 349-362

出版社

SPRINGER
DOI: 10.1007/s00418-021-02016-6

关键词

Putative stem cells; Cell differentiation; Endothelial cells; Ovary; Pig

资金

  1. National Science Centre Poland [UMO-2016/21/N/NZ9/01205]
  2. Society for Biology of Reproduction internship program

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The study demonstrated that porcine ovarian putative stem cells (poPSCs) have the potential to differentiate into endothelial cells (ECs) and develop capillary networks under appropriate induction, indicating their suitability as a potential source of ECs for tissue engineering.
Endothelial cells (ECs), the primary component of the vasculature, play a crucial role in neovascularization. However, the number of endogenous ECs is inadequate for both experimental purposes and clinical applications. Porcine ovarian putative stem cells (poPSCs), although not pluripotent, are characterized by great plasticity. Therefore, this study aimed to investigate whether poPSCs have the potential to differentiate into cells of endothelial lineage. poPSCs were immunomagnetically isolated from postnatal pig ovaries based on the presence of SSEA-4 protein. Expression of mesenchymal stem cells (MSCs) markers after pre-culture, both at the level of mRNA: ITGB1, THY, and ENG and corresponding protein: CD29, CD90, and CD105 were significantly higher compared to the control ovarian cortex cells. To differentiate poPSCs into ECs, inducing medium containing vascular endothelial growth factor (VEGF), basic fibroblast growth factor (bFGF), insulin-like growth factor (IGF), epidermal growth factor (EGF), ascorbic acid, and heparin was applied. After 14 days, poPSC differentiation into ECs was confirmed by immunofluorescence staining for vascular endothelial cadherin (VECad) and vascular endothelial growth factor receptor-2 (VEGFR-2). Semi-quantitative WB analysis of these proteins confirmed their high abundance. Additionally, qRT-PCR showed that mRNA expression of corresponding marker genes: CDH5, KDR was significantly higher compared with undifferentiated poPSCs. Finally, EC functional status was confirmed by the migration test that revealed that they were capable of positive chemotaxis, while tube formation assay demonstrated their ability to develop capillary networks. In conclusion, our results provided evidence that poPSCs may constitute the MSC population in the ovary and confirmed that they might be a potential source of ECs for tissue engineering.

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