Key Laboratory of Biomechanics and Mechanobiology (Beihang University), Ministry of Education, Beijing Advanced Innovation Center for Biomedical Engineering, School of Biological Science and Medical Engineering, Beihang University, Beijing, 100083, China.
Cell Mol Life Sci. 2022 Oct 16;79(11):551. doi: 10.1007/s00018-022-04591-w.
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) 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.
牙周膜(PDL)细胞是牙周再生治疗的有前途的工具。获得足够数量的 PDL 细胞对于 PDL 再生至关重要。在我们的研究中,适当的流切应力(FSS,1-6 dyn/cm)可促进 PDL 细胞的增殖。FSS 以时间依赖性方式重塑细胞骨架和焦点粘连。FSS 在 10 分钟内诱导 PDL 细胞形成肌动球蛋白帽,使核变平,并增加核孔大小,从而促进 Yes 相关蛋白(YAP)的核转位。FSS 激活 p38,其在 YAP 调节中起双重作用。p38 调节 Akt 和丝切蛋白的磷酸化,以及诱导 F-肌动蛋白聚合以诱导 YAP 活性。此外,p38 抑制 pLATS,并连续调节血管运动蛋白(AMOT)和 YAP 的磷酸化。AMOT 竞争性地与 F-肌动蛋白和 YAP 结合,参与 FSS 介导的 YAP 核转位和细胞增殖。总的来说,我们的结果提供了对 p38-AMOT-YAP 在 FSS 介导的 PDL 细胞增殖中的作用的机制见解,并表明其在牙科再生医学中有潜在的应用。