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Fluid shear stress promotes periodontal ligament cells proliferation via p38-AMOT-YAP.

Qiusheng ShiLisha ZhengJing NaXinyang LiZhijie YangXinyuan ChenYaxin SongChiyu LiLulin ZhouYubo Fan
Published in: Cellular and molecular life sciences : CMLS (2022)
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/cm 2 ) 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.
Keyphrases
  • induced apoptosis
  • cell cycle arrest
  • signaling pathway
  • cell proliferation
  • stem cells
  • endoplasmic reticulum stress
  • climate change
  • cystic fibrosis
  • cell therapy
  • cell migration
  • drug induced