Stretch-activated ion channel Piezo1 directs lineage choice in human neural stem cells

被引:482
作者
Pathak, Medha M. [1 ]
Nourse, Jamison L. [2 ,4 ]
Truc Tran [1 ]
Hwe, Jennifer [1 ]
Arulmoli, Janahan [3 ,4 ]
Le, Dai Trang T. [1 ]
Bernardis, Elena [5 ]
Flanagan, Lisa A. [2 ,3 ,4 ]
Tombola, Francesco [1 ]
机构
[1] Univ Calif Irvine, Dept Physiol & Biophys, Irvine, CA 92697 USA
[2] Univ Calif Irvine, Dept Neurol, Irvine, CA 92697 USA
[3] Univ Calif Irvine, Dept Biomed Engn, Irvine, CA 92697 USA
[4] Univ Calif Irvine, Sue & Bill Gross Stem Cell Res Ctr, Irvine, CA 92697 USA
[5] Childrens Hosp Philadelphia, Dept Pediat, Dermatol Sect, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
matrix mechanics; calcium signaling; myosin II; Yap/Taz; blebbistatin; PROGENITOR CELLS; SUBSTRATE; CULTURE; IDENTIFICATION; COMMITMENT; MECHANISMS; INHIBITOR; PATHWAY; TENSION; MATRIX;
D O I
10.1073/pnas.1409802111
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Neural stem cells are multipotent cells with the ability to differentiate into neurons, astrocytes, and oligodendrocytes. Lineage specification is strongly sensitive to the mechanical properties of the cellular environment. However, molecular pathways transducing matrix mechanical cues to intracellular signaling pathways linked to lineage specification remain unclear. We found that the mechanically gated ion channel Piezo1 is expressed by brain-derived human neural stem/progenitor cells and is responsible for a mechanically induced ionic current. Piezo1 activity triggered by traction forces elicited influx of Ca2+, a known modulator of differentiation, in a substrate-stiffness-dependent manner. Inhibition of channel activity by the pharmacological inhibitor GsMTx-4 or by siRNA-mediated Piezo1 knockdown suppressed neurogenesis and enhanced astrogenesis. Piezo1 knockdown also reduced the nuclear localization of the mechanoreactive transcriptional coactivator Yes-associated protein. We propose that the mechanically gated ion channel Piezo1 is an important determinant of mechanosensitive lineage choice in neural stem cells and may play similar roles in other multipotent stem cells.
引用
收藏
页码:16148 / 16153
页数:6
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