Connective tissue growth factor promotes cell-to-cell communication in human periodontal ligament stem cells via MAPK and PI3K pathway

被引:12
作者
Wu, Zuping [1 ,2 ]
Chen, Sirui [1 ,2 ]
He, Yuying [1 ,2 ]
Zhang, Demao [1 ]
Zou, Shujuan [1 ,2 ]
Xie, Jing [1 ]
Zhou, Chenchen [1 ,2 ]
机构
[1] Sichuan Univ, West China Hosp Stomatol, State Key Lab Oral Dis, Chengdu 610064, Sichuan, Peoples R China
[2] Sichuan Univ, West China Hosp Stomatol, Natl Clin Res Ctr Oral Dis, Dept Orthodont,State Key Lab Oral Dis, Chengdu, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
cell communication; connective tissue growth factor; gap junctions; periodontal ligament; GAP-JUNCTION; INTERCELLULAR COMMUNICATION; SIGNAL-TRANSDUCTION; DENTAL-PULP; EXPRESSION; CONNEXIN-43; DIFFERENTIATION; CONTRIBUTES; ROLES; PANNEXINS;
D O I
10.1002/JPER.21-0339
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Background Cell-cell communication is an essential process to respond to biological stimuli and sustain the micro environmental homeostasis of human periodontal ligament stem cells (hPDLSCs). Connective tissue growth factor (CTGF), a critical secreted matrix protein, exhibits significant tasks in regulating the cell-cell and cell-matrix interactions. This study aimed to explore the relationship between CTGF and cell communication and the underlying mechanism. Methods qRT-PCR was used to detect CCN family, connexin, and pannexin family expression in hPDLSCs. Stimulation with CTGF, cell migration assay was performed to examine the wound repair. The scrape loading/dye transfer assay was employed to access lucifer Yellow molecules transfer efficiency mediated by cell-cell communication. Connexin43 (Cx43), Pannexin1 (Panx1), MAPK, and the PI3K/Akt signaling pathway proteins were examined via Western blotting. Immunofluorescence was applied to visualize the localization of specific proteins within cells. Corresponding pathway inhibitors were applied to hPDLSCs to detect Cx43, Panx1 expression, and intercellular communication induced by CTGF. Results Our result showed that CTGF was the second most expressed CCN family member in hPDLSCs. Cx43, and Panx1 were the most widely expressed gap junction hemichannels in hPDLSCs. CTGF enhanced hPDLSCs migration in a dose-dependent manner. CTGF promoted cell-cell communication by up-regulating Cx43 and Panx1. CTGF induced Akt, JNK, and p38 phosphorylation and subcellular relocation. Inhibiting corresponding pathways reduced Cx43 expression, thereby weakening CTGF-induced cell-cell communication. However, the Panx1 expression in CTGF-treated hPDLSCs mainly depended on PI3K/Akt signaling. Conclusion We provided novel evidence that CTGF promoted cell-cell communication in hPDLSCs through MAPK and PI3K pathway.
引用
收藏
页码:E60 / E72
页数:13
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