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A critical role of the K(Ca)3.1 channel in mechanical stretch‐induced proliferation of rat bone marrow‐derived mesenchymal stem cells

Mechanical stimulation is an important factor regulating mesenchymal stem cell (MSC) functions such as proliferation. The Ca(2+)‐activated K(+) channel, K(Ca)3.1, is critically engaged in MSC proliferation but its role in mechanical regulation of MSC proliferation remains unknown. Here, we examined...

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Detalles Bibliográficos
Autores principales: Jia, Xiaoling, Su, Hao, Chen, Xinlan, Huang, Yangbi, Zheng, Yufan, Ji, Pei, Gao, Chao, Gong, Xianghui, Huang, Yan, Jiang, Lin‐Hua, Fan, Yubo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7131943/
https://www.ncbi.nlm.nih.gov/pubmed/32065503
http://dx.doi.org/10.1111/jcmm.15014
Descripción
Sumario:Mechanical stimulation is an important factor regulating mesenchymal stem cell (MSC) functions such as proliferation. The Ca(2+)‐activated K(+) channel, K(Ca)3.1, is critically engaged in MSC proliferation but its role in mechanical regulation of MSC proliferation remains unknown. Here, we examined the K(Ca)3.1 channel expression and its role in rat bone marrow‐derived MSC (BMSC) proliferation in response to mechanical stretch. Application of mechanical stretch stimulated BMSC proliferation via promoting cell cycle progression. Such mechanical stimulation up‐regulated the K(Ca)3.1 channel expression and pharmacological or genetic inhibition of the K(Ca)3.1 channel strongly suppressed stretch‐induced increase in cell proliferation and cell cycle progression. These results support that the K(Ca)3.1 channel plays an important role in transducing mechanical forces to MSC proliferation. Our finding provides new mechanistic insights into how mechanical stimuli regulate MSC proliferation and also a viable bioengineering approach to improve MSC proliferation.