| Literature DB >> 30044986 |
Quinton Smith1, Bria Macklin1, Xin Yi Chan1, Hannah Jones1, Michelle Trempel1, Mervin C Yoder2, Sharon Gerecht3.
Abstract
The role of primary cilia in mechanosensation is essential in endothelial cell (EC) shear responsiveness. Here, we find that venous, capillary, and progenitor ECs respond to shear stress in vitro in a cilia-dependent manner. We then demonstrate that primary cilia assembly in human induced pluripotent stem cell (hiPSC)-derived ECs varies between different cell lines with marginal influence of differentiation protocol. hiPSC-derived ECs lacking cilia do not align to shear stress, lack stress fiber assembly, have uncoordinated migration during wound closure in vitro, and have aberrant calcium influx upon shear exposure. Transcriptional analysis reveals variation in regulatory genes involved in ciliogenesis among different hiPSC-derived ECs. Moreover, inhibition of histone deacetylase 6 (HDAC6) activity in hiPSC-ECs lacking cilia rescues cilia formation and restores mechanical sensing. Taken together, these results show the importance of primary cilia in hiPSC-EC mechano-responsiveness and its modulation through HDAC6 activity varies among hiPSC-ECs.Entities:
Keywords: endothelial cells; human induced pluripotent stem cells; microfluidics; primary cilia; shear stress; tissue engineering
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Year: 2018 PMID: 30044986 DOI: 10.1016/j.celrep.2018.06.083
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423