Institute for Reproductive Health and Regenerative Medicine, Department of Pathology and Laboratory Medicine, University of Kansas Medical Center, Kansas City, Kansas 66160, USA.
J Biol Chem. 2012 Jan 13;287(3):2257-68. doi: 10.1074/jbc.M111.287128. Epub 2011 Nov 28.
The morphogenesis of the hemochorial placenta is dependent upon the precise expansion and differentiation of trophoblast stem (TS) cells. SATB homeobox 1 (SATB1) and SATB2 are related proteins that have been implicated as regulators of some stem cell populations. SATB1 is highly expressed in TS cells, which prompted an investigation of SATB1 and the related SATB2 as regulators of TS cells. SATB1 and SATB2 were highly expressed in rat TS cells maintained in the stem state and rapidly declined following induction of differentiation. SATB proteins were also present within the rat placenta during early stages of its morphogenesis and disappeared as gestation advanced. Silencing Satb1 or Satb2 expression decreased TS cell self-renewal and increased differentiation, whereas ectopic expression of SATB proteins promoted TS cell expansion and blunted differentiation. Eomes, a key transcriptional regulator of TS cells, was identified as a target for SATB proteins. SATB knockdown decreased Eomes transcript levels and promoter activity, whereas SATB ectopic expression increased Eomes transcript levels and promoter activity. Electrophoretic mobility shift assay as well as chromatin immunoprecipitation analyses demonstrated that SATB proteins physically associate with a regulatory site within the Eomes promoter. We conclude that SATB proteins promote TS cell renewal and inhibit differentiation. These actions are mediated in part by regulating the expression of the TS cell stem-associated transcription factor, EOMES.
合胞体胎盘的形态发生依赖于滋养层干细胞 (TS) 细胞的精确扩张和分化。SATB 同源盒 1 (SATB1) 和 SATB2 是相关蛋白,它们被认为是一些干细胞群体的调节因子。SATB1 在 TS 细胞中高度表达,这促使我们研究 SATB1 和相关的 SATB2 作为 TS 细胞的调节因子。SATB1 和 SATB2 在维持干细胞状态的大鼠 TS 细胞中高度表达,在诱导分化后迅速下降。SATB 蛋白也存在于大鼠胎盘的早期形态发生过程中,并随着妊娠的进展而消失。沉默 Satb1 或 Satb2 的表达会降低 TS 细胞的自我更新能力并增加分化,而 SATB 蛋白的异位表达则促进 TS 细胞的扩增并减弱分化。Eomes 是 TS 细胞的关键转录调节因子,被鉴定为 SATB 蛋白的靶标。SATB 敲低降低了 Eomes 转录本水平和启动子活性,而 SATB 异位表达增加了 Eomes 转录本水平和启动子活性。电泳迁移率变动分析和染色质免疫沉淀分析表明,SATB 蛋白与 Eomes 启动子内的一个调节位点发生物理关联。我们得出结论,SATB 蛋白促进 TS 细胞更新并抑制分化。这些作用部分是通过调节 TS 细胞干细胞相关转录因子 EOMES 的表达来介导的。