Silencing integrin α6 enhances the pluripotency-differentiation transition in human dental pulp stem cells

被引:6
作者
Zhang, Weiwei [1 ,2 ]
Shen, Jingling [3 ]
Zhang, Shuang [1 ,2 ]
Liu, Xu [4 ]
Pan, Shuang [1 ,2 ]
Li, Yanping [1 ,2 ]
Zhang, Lin [1 ,2 ]
He, Lina [1 ,2 ]
Niu, Yumei [1 ,2 ]
机构
[1] Harbin Med Univ, Dept Endodont, Affiliated Hosp 1, Harbin 150001, Peoples R China
[2] Harbin Med Univ, Sch Stomatol, Dept Endodont, Harbin, Peoples R China
[3] Wenzhou Univ, Inst Life Sci, Wenzhou, Peoples R China
[4] Harbin Med Univ, Dept Stomatol, Affiliated Hosp 4, Harbin, Peoples R China
基金
中国国家自然科学基金;
关键词
dental pulp stem cells; differentiation; integrin α 6; pluripotency; RHO; ROCK signaling pathway; KINASE INHIBITOR Y-27632; EXTRACELLULAR-MATRIX; ENDOTHELIAL-CELLS; PROMOTES; PROLIFERATION; SCAFFOLDS; MIGRATION; CULTURE; NICHE; HISAT;
D O I
10.1111/odi.13771
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Objectives Although integrins have been shown to be associated with proliferation and differentiation in some stem cells, the regulatory effect of integrin alpha 6 (ITG alpha 6) on the human dental pulp stem cells (hDPSCs) has not been reported. Here, we detected the roles of ITG alpha 6 in hDPSCs. Materials and methods Attached to Cytodex 3 microcarriers, hDPSCs grown under stimulated microgravity (SMG) or conventional culture conditions were measured the proliferation and different gene expression. Further, ITG alpha 6 was silenced in hDPSCs, and its effect on proliferation, differentiation, and cytoskeletal organization was analyzed. Results SMG conditions increased the number of Ki67-positive hDPSCs and progression into S phase of cell cycle. WB analysis showed the expression of ITG alpha 6 was upregulated in hDPSCs under SMG conditions. Knockdown of ITG alpha 6 decreased the expression of stemness markers, CD105 and STRO-1 in hDPSCs, but promoted the osteogenic and odontogenic differentiation by increased ALP expression and Alizarin Red nodules. Moreover, RNA-seq demonstrated that RHO/ROCK signaling pathway upregulated silencing ITG alpha 6-hDPSCs. Treatment with Y-27632 inhibited the effect of ITG alpha 6 depletion on hDPSCs stemness, rearranged the cytoskeleton, promoted the pluripotency, proliferation ability, and inhibited the differentiation. Conclusion ITG alpha 6 promotes hDPSCs stemness via inhibiting RHO/ROCK and restoring cytoskeleton.
引用
收藏
页码:711 / 722
页数:12
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