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碱性成纤维细胞生长因子通过白细胞介素-6调控人脱落乳牙来源干细胞中REX1的表达。

Basic Fibroblast Growth Factor Regulates REX1 Expression Via IL-6 In Stem Cells Isolated From Human Exfoliated Deciduous Teeth.

作者信息

Nowwarote Nunthawan, Sukarawan Waleerat, Pavasant Prasit, Osathanon Thanaphum

机构信息

Graduate Program in Oral Biology, Faculty of Dentistry, Chulalongkorn University, Bangkok, 10330, Thailand.

Mineralized Tissue Research Unit, Faculty of Dentistry, Chulalongkorn University, Bangkok, 10330, Thailand.

出版信息

J Cell Biochem. 2017 Jun;118(6):1480-1488. doi: 10.1002/jcb.25807. Epub 2016 Dec 29.

Abstract

Basic fibroblast growth factor (bFGF) regulates pluripotent marker expression and cellular differentiation in various cell types. However, the mechanism by which bFGF regulates REX1 expression in stem cells, isolated from human exfoliated deciduous teeth (SHEDs) remains unclear. The aim of the present study was to investigate the regulation of REX1 expression by bFGF in SHEDs. SHEDs were isolated and characterized. Their mRNA and protein expression levels were determined using real-time polymerase chain reaction and enzyme-linked immunosorbent assay, respectively. In some experiments, chemical inhibitors were added to the culture medium to impede specific signaling pathways. Cells isolated from human exfoliated deciduous tooth dental pulp tissue expressed mesenchymal stem cell surface markers (CD44, CD73, CD90, and CD105). These cells differentiated into osteogenic and adipogenic lineages, when appropriately induced. Treating SHEDs with bFGF induced REX1 mRNA expression and this effect was attenuated by pretreatment with FGFR or Akt inhibitors. Cycloheximide pretreatment also inhibited the bFGF-induced REX1 expression, implying the involvement of intermediate molecule(s). Further, the addition of an IL-6 neutralizing antibody attenuated the bFGF-induced REX1 expression by SHEDs. In conclusion, bFGF enhanced REX1 expression by SHEDs via the FGFR and Akt signaling pathways. Moreover, IL-6 participated in the bFGF-induced REX1 expression in SHEDs. J. Cell. Biochem. 118: 1480-1488, 2017. © 2016 Wiley Periodicals, Inc.

摘要

碱性成纤维细胞生长因子(bFGF)可调节多种细胞类型中多能性标志物的表达和细胞分化。然而,bFGF调节从人脱落乳牙(SHEDs)分离出的干细胞中REX1表达的机制仍不清楚。本研究的目的是探讨bFGF对SHEDs中REX1表达的调节作用。分离并鉴定了SHEDs。分别使用实时聚合酶链反应和酶联免疫吸附测定法测定其mRNA和蛋白质表达水平。在一些实验中,向培养基中添加化学抑制剂以阻断特定的信号通路。从人脱落乳牙牙髓组织分离出的细胞表达间充质干细胞表面标志物(CD44、CD73、CD90和CD105)。这些细胞在适当诱导时可分化为成骨和成脂谱系。用bFGF处理SHEDs可诱导REX1 mRNA表达,而用FGFR或Akt抑制剂预处理可减弱这种作用。放线菌酮预处理也抑制了bFGF诱导的REX1表达,这意味着有中间分子参与。此外,添加IL-6中和抗体可减弱bFGF诱导的SHEDs中REX1的表达。总之,bFGF通过FGFR和Akt信号通路增强了SHEDs中REX1的表达。此外,IL-6参与了bFGF诱导的SHEDs中REX1的表达。《细胞生物化学杂志》118: 1480 - 1488, 2017。© 2016威利期刊公司

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