| Literature DB >> 36244032 |
Qiusheng Shi1, Lisha Zheng2, Jing Na1, Xinyang Li1, Zhijie Yang1, Xinyuan Chen1, Yaxin Song1, Chiyu Li1, Lulin Zhou1, Yubo Fan3.
Abstract
Periodontal ligament (PDL) cells are a promising tool for periodontal regeneration therapy. Achieving a sufficient number of PDL cells is essential to PDL regeneration. In our study, appropriate flow shear stress (FSS, 1-6 dyn/cm2) promotes the proliferation of PDL cells. FSS remodels cytoskeleton and focal adhesion in a duration-dependent manner. FSS induces PDL cells to form the actin cap within 10 min, flattens the nuclei, and increases the nuclear pore size, which promotes nuclear translocation of Yes-associated protein (YAP). FSS activates p38, which plays a dual function in YAP regulation. p38 regulates the phosphorylation of Akt and cofilin, as well as induced F-actin polymerization to induce YAP activity. In addition, p38 inhibits pLATS and consecutively regulates angiomotin (AMOT) and YAP phosphorylation. AMOT competitively binds to F-actin and YAP to participate in FSS-mediated YAP nuclear translocation and cell proliferation. Taken collectively, our results provide mechanistic insights into the role of p38-AMOT-YAP in FSS-mediated PDL cells proliferation and indicate potential applications in dental regenerative medicine.Entities:
Keywords: Biomechanics; LINC; Mechanotransduction; Nuclear changes; Nuclear-cytoplasmic translocation
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Year: 2022 PMID: 36244032 DOI: 10.1007/s00018-022-04591-w
Source DB: PubMed Journal: Cell Mol Life Sci ISSN: 1420-682X Impact factor: 9.207