Platelet endothelial aggregation receptor-1 (PEAR1) is involved in C2C12 myoblast differentiation

被引:13
|
作者
Cui, Ya Feng [1 ]
Yan, Yun Qin [1 ]
Liu, Dan [1 ]
Pang, Yu Sheng [1 ]
Wu, Jiang [1 ]
Li, Shu Feng [1 ]
Tong, Hui Li [1 ]
机构
[1] Northeast Agr Univ, Lab Cell & Dev Biol, Harbin 150030, Heilongjiang, Peoples R China
关键词
PEAR1; C2C12; differentiation; muscle; EARLY-ONSET MYOPATHY; SKELETAL-MUSCLE; RESPIRATORY-DISTRESS; DYSPHAGIA EMARDD; STEM-CELLS; MYOGENESIS; MEGF10; ACTIVATION; EXPRESSION; REGENERATION;
D O I
10.1016/j.yexcr.2018.03.027
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
C2C12 murine myoblasts are a common model for studying muscle differentiation. Platelet endothelial aggregation receptor-1 (PEAR1), an epidermal growth factor repeat-containing transmembrane receptor, is known to participate in platelet contact-induced activation. In the present study, we demonstrated that PEAR1 is involved in the differentiation of C2C12 murine myoblasts. Western blotting and immunofluorescence staining were used to determine PEAR1 expression and localization during C2C12 cell differentiation. Subsequently, PEAR1 expression was activated and inhibited using clustered regularly interspaced short palindromic repeatsd-Cas9 technology to explore its effects on this process. PEAR1 expression was found to increase over the course of C2C12 cell differentiation. This protein was predominately localized on the membrane of these cells, where it clustered upon induction of differentiation. Expression of the myogenic markers Desmin, MYOG, and MYH2 revealed that PEAR1 positively regulated C2C12 cell differentiation. Moreover, induction of muscle injury by administration of bupivacaine to mice indicated that PEAR1 might play a role in muscle regeneration. In summary, our study confirmed the involvement of PEAR1 in C2C12 cell differentiation, contributing to our understanding of the molecular mechanisms underlying muscle development.
引用
收藏
页码:199 / 204
页数:6
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