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SFRP2 enhanced the adipogenic and neuronal differentiation potentials of stem cells from apical papilla
Author(s) -
Lin Xiao,
Dong Rui,
Diao Shu,
Yu Guoxia,
Wang Liping,
Li Jun,
Fan Zhipeng
Publication year - 2017
Publication title -
cell biology international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.932
H-Index - 77
eISSN - 1095-8355
pISSN - 1065-6995
DOI - 10.1002/cbin.10757
Subject(s) - adipogenesis , sox2 , wnt signaling pathway , microbiology and biotechnology , stem cell , mesenchymal stem cell , cellular differentiation , biology , multipotent stem cell , chemistry , signal transduction , embryonic stem cell , genetics , gene , progenitor cell
Dental tissue‐derived mesenchymal stem cells (MSCs) are easily obtained and considered as a favorable cell source for tissue engineering, but the regulation of direct differentiation is unknown, which restricts their application. The present study investigated the effect of SFRP2, a Wnt signaling modulator, on MSC differentiation using stem cells from apical papilla (SCAPs). The cells were cultured in specific inducing medium for adipogenic, neurogenic, or chondrogenic differentiation. Over‐expression of SFRP2 via retroviral infection enhanced the adipogenic and neurogenic differentiation of SCAPs. While inhibit of Wnt pathway by IWR1‐endo could enhance the neurogenic differentiation potentials of SCAPs, similar with the function of SFRP2. In addition, over‐expression of SFRP2 up‐regulated the expression of stemness‐related genes SOX2 and OCT4 . Furthermore, SOX2 and OCT4 expression was significantly inhibited after lentiviral silencing of SFRP2 in SCAPs. Therefore, our results suggest that SFRP2 enhances the adipogenic and neurogenic differentiation potentials of SCAPs by up‐regulating SOX2 and OCT4 . Moreover, the effect of SFRP2 in neurogenic differentiation of SCAPs maybe also associated with Wnt inhibition. Our results provided useful information about the molecular mechanism underlying directed differentiation in dental tissue‐derived MSCs.