RETRACTED: Role of the P2X7 receptor in inflammation-mediated changes in the osteogenesis of periodontal ligament stem cells (Retracted Article)

被引:54
|
作者
Xu, Xin-Yue [1 ,2 ]
He, Xiao-Tao [1 ,2 ]
Wang, Jia [1 ,2 ]
Li, Xuan [1 ,2 ]
Xia, Yu [1 ,2 ]
Tan, Yi-Zhou [1 ,2 ]
Chen, Fa-Ming [1 ,2 ]
机构
[1] Fourth Mil Med Univ, State Key Lab Mil Stomatol, Natl Clin Res Ctr Oral Dis, Sch Stomatol, Xian 710032, Shaanxi, Peoples R China
[2] Fourth Mil Med Univ, Shaanxi Engn Res Ctr Dent Mat & Adv Manufacture, Dept Periodontol, Sch Stomatol, Xian 710032, Shaanxi, Peoples R China
关键词
BONE-MARROW; EXTRACELLULAR ATP; P2X(7) RECEPTOR; TNF-ALPHA; IN-VITRO; DIFFERENTIATION; PROLIFERATION; EXPRESSION; OSTEOBLAST; NUCLEOTIDES;
D O I
10.1038/s41419-018-1253-y
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Accumulating evidence indicates that the pluripotency of periodontal ligament stem cells (PDLSCs) is compromised under inflammatory conditions; however, the underlying mechanisms remain largely unexplored. In this study, we hypothesize that the P2X7 receptor (P2X7R) is a key molecule linked to inflammation-associated impairment of PDLSCs. We first investigated P2X7R expression in PDLSCs under normal and inflammatory conditions and then determined the effect of a P2X7R agonist (BzATP) or antagonist (BBG) on PDLSC osteogenesis under various conditions. Gene-modified PDLSCs were used to further examine the role of P2X7R and the signaling pathway underlying P2X7R-enhanced osteogenesis. We found that inflammatory conditions decreased P2X7R expression in PDLSCs and reduced osteogenesis in these cells. In addition, activation of P2X7R by BzATP or overexpression of P2X7R via gene transduction reversed the inflammation-mediated decrease in PDLSC osteogenic differentiation. When selected osteogenesis-related signaling molecules were screened, the PI3K-AKT-mTOR pathway was identified as potentially involved in P2X7R-enhanced PDLSC osteogenesis. Our data reveal a crucial role for P2X7R in PDLSC osteogenesis under inflammatory conditions, suggesting a new therapeutic target to reverse or rescue inflammation-mediated changes in PDLSCs for future mainstream therapeutic uses.
引用
收藏
页数:17
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