Lithium chloride promotes the odontoblast differentiation of hair follicle neural crest cells by activating Wnt/β-catenin signaling

被引:19
|
作者
Shan, Tengfei [1 ,3 ]
Zhou, Cheng [1 ,4 ]
Yang, Rong [2 ]
Yan, Fei [2 ]
Zhang, Ping [1 ,2 ]
Fu, Yu [1 ,2 ]
Jiang, Hongbing [1 ,2 ]
机构
[1] Nanjing Med Univ, Sch Stomatol, Inst Stomatol, Nanjing 210029, Jiangsu, Peoples R China
[2] Nanjing Med Univ, Sch Stomatol, Dept Oral & Maxillofacial Surg, Nanjing 210029, Jiangsu, Peoples R China
[3] Southeast Univ, Coll Med, Zhongda Hosp, Dept Oral & Maxillofacial Surg, Nanjing 210009, Peoples R China
[4] Wuxi Fourth Peoples Hosp, Dept Oral & Maxillofacial Surg, Wuxi 214062, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
lithium chloride; neural crest cells; odontoblast differentiation; Wnt; -catenin; MESENCHYMAL STEM-CELLS; IN-VITRO; REGENERATIVE MEDICINE; TOOTH REGENERATION; PROLIFERATION; EXPRESSION; MECHANISM; SCAFFOLD; PATHWAY; TISSUES;
D O I
10.1002/cbin.10340
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The Wnt/-catenin signalling pathway contributes to the maintenance of pluripotency and partial reprogramming of stem cells. Postnatal neural crest cells (NCCs) can differentiate into odontoblast-like cells due to their multi-potential property, but further endeavors need to be made to promote odontogenic differentiation of hair follicle neural crest cells (hfNCCs). This study investigated whether the Wnt pathway activator lithium chloride (LiCl) promotes odontoblast differentiation of hfNCCs. Change of proliferation, -catenin and pluripotency markers of hfNCCs were examined after treatment with LiCl. An in vitro odontoblast differentiation model of hfNCCs was built using dental cell conditioned media (DC-CM). The effects of LiCl on odontoblast differentiation of hfNCCs showed that proliferation and expression of -catenin in the cytosolic and nuclear compartments were increased in the LiCl-treated hfNCCs, and the pluripotency marks, Oct4, Klf4, Sox2 and Nanog, were more highly expressed in the LiCl-treated group than in the control group. The odontoblast markers such as DSP, DMP1 and Runx2, could be detected in hfNCCs induced by DC-CM, but in LiCl -treated group all three markers had stronger expression. Expression of -catenin in the nuclear of LiCl-treated hfNCCs induced by DC-CM was higher than in the other groups. The data indicate that the Wnt pathway activator LiCl can promote proliferation and odontoblast differentiation of hfNCCs, and chemical approaches are of benefit in obtaining more desirable seed cell types for cell-based therapies.
引用
收藏
页码:35 / 43
页数:9
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