Division of Oral Biotechnology, Center for Dental Medicine, Medical Center-University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Department of Orthodontics, Center for Dental Medicine, Medical Center-University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
J Dent Res. 2021 Oct;100(11):1210-1219. doi: 10.1177/00220345211007855. Epub 2021 Apr 17.
Novel findings broaden the concept of mechanotransduction (MT) in biophysically stimulated tissues such as the periodontium by considering nuclear MT, convergence of intracellular MT pathways, and mechanoresponsive cotranscription factors such as Yes-associated protein 1 (YAP1). Regarding periodontal disease, recent studies have elucidated the role of bacterial gingipain proteases in disturbing the barrier function of cadherins, thereby promoting periodontal inflammation. This leads to dysregulation of extracellular matrix homeostasis via proteases and changes the cell's biophysical environment, which leads to alterations in MT-induced cell behavior and loss of periodontal integrity. Newest experimental evidence from periodontal ligament cells suggests that the Hippo signaling protein YAP1, in addition to integrin-FAK (focal adhesion kinase) mechanosignaling, also regulates cell stemness. By addressing mechanosignaling-dependent transcription factors, YAP1 is involved in osteogenic and myofibroblast differentiation and influences core steps of autophagy. Recent in vivo evidence elucidates the decisive role of YAP1 in epithelial homeostasis and underlines its impact on oral pathologies, such as periodontitis-linked oral squamous cell carcinogenesis. Here, new insights reveal that YAP1 contributes to carcinogenesis via overexpression rather than mutation; promotes processes such as apoptosis resistance, epithelial-mesenchymal transition, or metastasis; and correlates with poor prognosis in oral squamous cell carcinoma. Furthermore, YAP1 has been shown to contribute to periodontitis-induced bone loss. Mechanistically, molecules identified to regulate YAP1-related periodontal homeostasis and disease include cellular key players such as MAPK (mitogen-activated protein kinase), JNK (c-Jun N-terminal kinase), Rho (Ras homologue) and ROCK (Rho kinase), Bcl-2 (B-cell lymphoma 2), AP-1 (activator protein 1), and c-myc (cellular myelocytomatosis). These findings qualify YAP1 as a master regulator of mechanobiology and cell behavior in human periodontal tissues. This review summarizes the most recent developments in MT-related periodontal research, thereby offering insights into outstanding research questions and potential applications of molecular or biophysical strategies aiming at periodontal disease mitigation or prevention.
新发现拓宽了生物物理刺激组织(如牙周组织)的力学转导(MT)概念,包括核 MT、细胞内 MT 途径的收敛以及机械反应性共转录因子,如 YAP1(Yes 相关蛋白 1)。关于牙周病,最近的研究阐明了细菌牙龈蛋白酶在干扰钙黏蛋白的屏障功能方面的作用,从而促进牙周炎。这导致细胞外基质稳态通过蛋白酶失调,并改变细胞的生物物理环境,从而导致 MT 诱导的细胞行为改变和牙周完整性丧失。牙周韧带细胞的最新实验证据表明,Hippo 信号蛋白 YAP1 除了整合素-FAK(粘着斑激酶)机械信号外,还调节细胞干性。通过解决依赖机械信号的转录因子,YAP1 参与成骨和肌成纤维细胞分化,并影响自噬的核心步骤。最近的体内证据阐明了 YAP1 在上皮稳态中的决定性作用,并强调了其对口腔病理学的影响,如牙周病相关的口腔鳞状细胞癌发生。在这里,新的见解表明,YAP1 通过过表达而不是突变促进致癌作用;促进凋亡抵抗、上皮-间充质转化或转移等过程;并与口腔鳞状细胞癌的预后不良相关。此外,已经表明 YAP1 有助于牙周炎引起的骨丢失。从机制上讲,鉴定出调节 YAP1 相关牙周稳态和疾病的分子包括细胞关键因子,如 MAPK(丝裂原激活蛋白激酶)、JNK(c-Jun N 末端激酶)、Rho(Ras 同源物)和 ROCK(Rho 激酶)、Bcl-2(B 细胞淋巴瘤 2)、AP-1(激活蛋白 1)和 c-myc(细胞髓细胞瘤病毒)。这些发现使 YAP1 成为人类牙周组织力学生物学和细胞行为的主要调节剂。本综述总结了与 MT 相关的牙周研究的最新进展,从而为减轻或预防牙周病的分子或生物物理策略的突出研究问题和潜在应用提供了见解。