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miR-294/302家族对上皮-间质转化和凋亡途径的抑制协同阻断了let-7诱导的胚胎干细胞自我更新沉默。

Suppression of epithelial-mesenchymal transition and apoptotic pathways by miR-294/302 family synergistically blocks let-7-induced silencing of self-renewal in embryonic stem cells.

作者信息

Guo W-T, Wang X-W, Yan Y-L, Li Y-P, Yin X, Zhang Q, Melton C, Shenoy A, Reyes N A, Oakes S A, Blelloch R, Wang Y

机构信息

Peking-Tsinghua Center for Life Sciences, Institute of Molecular Medicine, Peking University, Beijing, China.

Department of Urology, Center of Reproductive Sciences, and the Eli and Edythe Broad Center for Regeneration Medicine and Stem Cell Research, University of California, San Francisco, CA, USA.

出版信息

Cell Death Differ. 2015 Jul;22(7):1158-69. doi: 10.1038/cdd.2014.205. Epub 2014 Dec 12.

Abstract

The embryonic stem cell (ESC)-enriched miR-294/302 family and the somatic cell-enriched let-7 family stabilizes the self-renewing and differentiated cell fates, respectively. The mechanisms underlying these processes remain unknown. Here we show that among many pathways regulated by miR-294/302, the combinatorial suppression of epithelial-mesenchymal transition (EMT) and apoptotic pathways is sufficient in maintaining the self-renewal of ESCs. The silencing of ESC self-renewal by let-7 was accompanied by the upregulation of several EMT regulators and the induction of apoptosis. The ectopic activation of either EMT or apoptotic program is sufficient in silencing ESC self-renewal. However, only combined but not separate suppression of the two programs inhibited the silencing of ESC self-renewal by let-7 and several other differentiation-inducing miRNAs. These findings demonstrate that combined repression of the EMT and apoptotic pathways by miR-294/302 imposes a synergistic barrier to the silencing of ESC self-renewal, supporting a model whereby miRNAs regulate complicated cellular processes through synergistic repression of multiple targets or pathways.

摘要

富含胚胎干细胞(ESC)的miR-294/302家族和富含体细胞的let-7家族分别稳定自我更新和分化的细胞命运。这些过程背后的机制仍然未知。在这里,我们表明,在由miR-294/302调控的众多途径中,上皮-间质转化(EMT)和凋亡途径的组合抑制足以维持ESC的自我更新。let-7对ESC自我更新的沉默伴随着几种EMT调节因子的上调和凋亡的诱导。EMT或凋亡程序的异位激活足以沉默ESC的自我更新。然而,只有联合而非单独抑制这两个程序才能抑制let-7和其他几种诱导分化的miRNA对ESC自我更新的沉默。这些发现表明,miR-294/302对EMT和凋亡途径的联合抑制对ESC自我更新的沉默形成了协同障碍,支持了一种模型,即miRNA通过对多个靶标或途径的协同抑制来调节复杂的细胞过程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd13/4572863/9ff79cc5b89b/cdd2014205f1.jpg

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