| Literature DB >> 26694636 |
Kaixiang Yang1,2, Yingxing Wu1, Peng Cheng1, Jinming Zhang1, Chengyuan Yang2, Bin Pi2, Yaping Ye1, Hongbo You1, Anmin Chen1, Tao Xu3, Fengjing Guo1, Jun Qi1.
Abstract
Yes-associated protein (YAP) and extracellular signal-regulated kinase (ERK) have been considered as key regulators in tissue homeostasis, organ development, and tumor formation. However, the roles of YAP and ERK in the mediating strain mechanosensing in the growth plate cartilage have not been determined. In this study, chondrocytes obtained from the growth plate cartilage of 2-week-old Sprague-Dawley rats were subjected to the mechanical strain with different magnitudes and durations at a frequency of 0.5 Hz. We found that YAP and ERK activation in response to mechanical strain was time and magnitude dependent. Pretreatment with a RhoA inhibitor (C3 toxin) or a microfilament cytoskeleton disrupting reagent (cytochalasin D) could suppress their activation. In addition, activated YAP and ERK were able to induce cell cycle progression by up-regulating the expression of cell cycle-related genes. These results shed new light on the function of YAP and ERK in mechanical strain-promoted growth plate development. Our results also provided evidence that RhoA and cytoskeletal dynamics are required for this mechanotransduction.Entities:
Keywords: extracellular signal-regulated kinase (ERK); growth plate chondrocytes; mechanical strain; mechanotransduction; yes-associated protein (YAP)
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Year: 2016 PMID: 26694636 DOI: 10.1002/jor.23138
Source DB: PubMed Journal: J Orthop Res ISSN: 0736-0266 Impact factor: 3.494