4.6 Article

Differentiation of CD45-/CD31+ lung side population cells into endothelial and smooth muscle cells in vitro

期刊

INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
卷 43, 期 3, 页码 1128-1138

出版社

SPANDIDOS PUBL LTD
DOI: 10.3892/ijmm.2019.4053

关键词

side population cells; lung; endothelial cells; smooth muscle cells; stem cells

资金

  1. National Natural Science Foundation of China [81370619]

向作者/读者索取更多资源

Side population (SP) cells are a small subpopulation of cells found in many mammalian tissues and organs, identified by their capacity to efflux Hoechst 33342 dye. They are enriched for stem/progenitor cell activity. SP cells isolated from the adult mouse lung can be separated into a CD45(+) subset (bone marrow-derived) and a CD45(-) subset that can be subdivided into CD31(-) and CD31(+) subpopulations. CD45(-)/CD31(-) lung SP (LSP) cells are known to be mesenchymal stem cells. However, CD45(-)/CD31(+) LSP cells are not fully characterized. In the present study, it was found that CD45(-)/CD31(+) LSP cells were able to form colonies. Based on the expression of vascular endothelial growth factor receptor 2 (VEGFR2), these cells were separated into VEGFR2(-) and VEGFR2(+) cells. The CD45(-)/CD31(+)/VEGFR2(-) LSP cells expressed genes characteristic of smooth muscle and endothelial progenitors, and were able to differentiate into smooth muscle and endothelial cells in vitro. The CD45(-)/CD31(+)/VEGFR2(+) LSP cells expressed genes characteristic of endothelial progenitors and gave rise to endothelial cells, although not smooth muscle, in vitro. The data demonstrate that CD45(-)/CD31(+)/VEGFR2(-) LSP cells differentiated into CD45(-)/CD31(+)/VEGFR2(+) LSP cells and then endothelial cells, indicating that CD45(-)/CD31(+)/VEGFR2(+) LSP cells are likely to be derived from CD45(-)/CD31(+)/VEGFR2(-) LSP cells. Taken together, the results suggest that CD45(-)/CD31(+) LSP cells can be separated into CD45(-)/CD31(+)/VEGFR2(-) LSP cells, which may be progenitors of endothelial and smooth muscle, whereas CD45(-)/CD31(+)/VEGFR2(+) LSP cells may serve as late commitment endothelial progenitors in the adult mouse lung.

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