牙周纤维
细胞生物学
肌动蛋白
磷酸化
p38丝裂原活化蛋白激酶
焦点粘着
细胞骨架
化学
再生(生物学)
机械转化
肌动蛋白细胞骨架
蛋白激酶B
应力纤维
细胞生长
肌动蛋白解聚因子
细胞
生物
蛋白激酶A
医学
生物化学
牙科
作者
Qiusheng Shi,Lisha Zheng,Jing Na,Xinyang Li,Zhijie Yang,Xinyuan Chen,Yaxin Song,Chiyu Li,Lulin Zhou,Yubo Fan
标识
DOI:10.1007/s00018-022-04591-w
摘要
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.
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