Du Juan, Wu Yongyan, Ai Zhiying, Shi Xiaoyan, Chen Linlin, Guo Zekun
College of Life Sciences, Northwest A&F University, 3 Taicheng Road, Yangling 712100, Shaanxi, China; Key Laboratory of Animal Biotechnology, Ministry of Agriculture, Northwest A&F University, 3 Taicheng Road, Yangling 712100, Shaanxi, China.
College of Veterinary Medicine, Northwest A&F University, 3 Taicheng Road, Yangling 712100, Shaanxi, China; Key Laboratory of Animal Biotechnology, Ministry of Agriculture, Northwest A&F University, 3 Taicheng Road, Yangling 712100, Shaanxi, China.
Cell Signal. 2014 Oct;26(10):2107-16. doi: 10.1016/j.cellsig.2014.06.002. Epub 2014 Jun 18.
SB431542 (SB) is an established small molecular inhibitor that specifically binds to the ATP binding domains of the activin receptor-like kinase receptors, ALK5, ALK4 and ALK7, and thus specifically inhibits Smad2/3 activation and blocks TGF-β signal transduction. SB maintains the undifferentiated state of mouse embryonic stem cells. However, the way of SB in maintaining the undifferentiated state of mouse embryonic stem cells remains unclear. Considering that SB could not maintain embryonic stem cells pluripotency when leukemia inhibitory factor was withdrawn, we sought to identify the mechanism of SB on pluripotent maintenance. Transcripts regulated by SB, including message RNAs and small non-coding RNAs were examined through microarray and deep-sequence experiments. After examination, Western blot analysis, and quantitative real-time PCR verification, we found that SB regulated the transcript expressions related to self-renewal and differentiation. SB mainly functioned by inhibiting differentiation. The key pluripotent factors expression were not significantly affected by SB, and intrinsic differentiation-related transcripts including fibroblast growth factor family members, were significantly down-regulated by SB. Moreover, SB could partially inhibit the retinoic acid response to neuronal differentiation of mouse embryonic stem cells.
SB431542(SB)是一种已确定的小分子抑制剂,它特异性结合激活素受体样激酶受体ALK5、ALK4和ALK7的ATP结合结构域,从而特异性抑制Smad2/3激活并阻断TGF-β信号转导。SB维持小鼠胚胎干细胞的未分化状态。然而,SB维持小鼠胚胎干细胞未分化状态的方式仍不清楚。鉴于当白血病抑制因子撤除时SB无法维持胚胎干细胞多能性,我们试图确定SB在多能性维持方面的机制。通过微阵列和深度测序实验检测了受SB调控的转录本,包括信使RNA和小非编码RNA。经过检测、蛋白质免疫印迹分析和定量实时PCR验证,我们发现SB调控了与自我更新和分化相关的转录本表达。SB主要通过抑制分化发挥作用。关键多能因子的表达未受到SB的显著影响,而包括成纤维细胞生长因子家族成员在内的内在分化相关转录本则被SB显著下调。此外,SB可部分抑制小鼠胚胎干细胞对神经元分化的视黄酸反应。