HDAC3 is crucial in shear- and VEGF-induced stem cell differentiation toward endothelial cells

Lingfang Zeng, Qingzhong Xiao, Andriana Margariti, Zhongyi Zhang, Anna Zampetaki, Seema Patel, Maurizio C Capogrossi, Yanhua Hu, Qingbo Xu

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192 Citations (Scopus)

Abstract

Reendothelialization involves endothelial progenitor cell (EPC) homing, proliferation, and differentiation, which may be influenced by fluid shear stress and local flow pattern. This study aims to elucidate the role of laminar flow on embryonic stem (ES) cell differentiation and the underlying mechanism. We demonstrated that laminar flow enhanced ES cell-derived progenitor cell proliferation and differentiation into endothelial cells (ECs). Laminar flow stabilized and activated histone deacetylase 3 (HDAC3) through the Flk-1-PI3K-Akt pathway, which in turn deacetylated p53, leading to p21 activation. A similar signal pathway was detected in vascular endothelial growth factor-induced EC differentiation. HDAC3 and p21 were detected in blood vessels during embryogenesis. Local transfer of ES cell-derived EPC incorporated into injured femoral artery and reduced neointima formation in a mouse model. These data suggest that shear stress is a key regulator for stem cell differentiation into EC, especially in EPC differentiation, which can be used for vascular repair, and that the Flk-1-PI3K-Akt-HDAC3-p53-p21 pathway is crucial in such a process.
Original languageEnglish
Pages (from-to)1059-69
Number of pages11
JournalThe Journal of cell biology
Volume174
Issue number7
DOIs
Publication statusPublished - 2006

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    Zeng, L., Xiao, Q., Margariti, A., Zhang, Z., Zampetaki, A., Patel, S., Capogrossi, M. C., Hu, Y., & Xu, Q. (2006). HDAC3 is crucial in shear- and VEGF-induced stem cell differentiation toward endothelial cells. The Journal of cell biology, 174(7), 1059-69. https://doi.org/10.1083/jcb.200605113