4.7 Article

MiR-24-3p regulates the differentiation of adipose-derived stem cells toward pericytes and promotes fat grafting vascularization

Journal

FASEB JOURNAL
Volume 37, Issue 5, Pages -

Publisher

WILEY
DOI: 10.1096/fj.202202037RR

Keywords

adipose-derived stem cells; differentiation; fat grafting; pericytes; vascularization

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We induced adipose-derived stem cells (ADSCs) to differentiate into pericytes by treating them with conditional medium (CM) from endothelial cells (ECs) or human recombinant transforming growth factor beta (TGF-beta). The results showed that TGF-beta released by ECs promoted the migration, association with ECs, and expression of pericyte markers in ADSCs. MiR-24-3p directly targeted PDGFR beta in ADSCs and downregulating miR-24-3p promoted pericyte differentiation, migration, and association with ECs.
Adipose-derived stem cells (ADSCs) enhance fat graft survival by promoting neovascularization. The mechanism that promotes ADSCs differentiation toward pericytes was not known. We treated ADSCs with conditional medium (CM) from endothelial cells (ECs) or human recombinant transforming growth factor beta (TGF-beta) to induce differentiation into pericytes. Pericytes markers, including platelet-derived growth factor receptor beta (PDGFR beta), alpha-smooth muscle actin (alpha-SMA), and desmin, were examined. Pericytes differentiation markers, migration, and their association with ECs were examined in ADSCs transfected with miR-24-3p mimics and inhibitors. Bioinformatics target prediction platforms and luciferase assays were used to investigate whether PDGFR beta was directly targeted by miR-24-3p. In vivo, fat mixed with ADSCs transfected with miR-24-3p mimics or inhibitors was implanted subcutaneously on the lower back region of nude mice. Fat grafts were harvested and analyzed at 2, 4, 6, and 8 weeks. Results showed that endogenous TGF-beta derived from CM from EC or human recombinant TGF-beta promoted migration, association with ECs, and induced expression of pericyte markers (PDGFR beta, alpha-SMA, Desmin) in ADSCs. MiR-24-3p directly targeted PDGFR beta in ADSCs by lucifer reporter assays. Inhibition of miR-24-3p promoted pericytes differentiation, migration, and association with ECs in ADSCs. Inhibition of miR-24-3p in ADSCs promoted survival, integrity, adipocyte viability, vascularization, pericytes association with ECs, and reduced fibrosis, whereas overexpression of miR-24-3p in ADSCs yielded the opposite results. Collectively, TGF-beta released by ECs induced ADSCs differentiation toward pericytes through miR-24-3p. Downregulation of miR-24-3p in ADSCs induced survival, integrity, adipocyte viability, vascularization, pericytes association with ECs, and reduced fibrosis after fat grafting.

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