Inhibition of YAP/TAZ-TEAD activity induces cytotrophoblast differentiation into syncytiotrophoblast in human trophoblast.

IF 3.6 2区 医学 Q2 DEVELOPMENTAL BIOLOGY
Tetsuya Mizutani, Makoto Orisaka, Yumiko Miyazaki, Ririko Morichika, Miki Uesaka, Kaoru Miyamoto, Yoshio Yoshida
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引用次数: 2

Abstract

During placentation, placental cytotrophoblast (CT) cells differentiate into syncytiotrophoblast (ST) cells and extravillous trophoblast (EVT) cells. In the placenta, the expression of various genes is regulated by the Hippo pathway through a transcription complex, Yes-associated protein (YAP)/transcriptional coactivator with PDZ-binding motif (TAZ)-TEA domain transcription factor (TEAD) (YAP/TAZ-TEAD) activity. YAP/TAZ-TEAD activity is controlled by multiple factors and signaling, such as cAMP signaling. cAMP signaling is believed to be involved in the regulation of trophoblast function but is not yet fully understood. Here we showed that YAP/TAZ-TEAD expressions and their activities were altered by cAMP stimulation in BeWo cells, a human choriocarcinoma cell line. The repression of YAP/TAZ-TEAD activity induced the expression of ST-specific genes without cAMP stimulation, and transduction of constitutively active YAP, i.e. YAP-5SA, resulted in the repression of 8Br-cAMP-induced expressions of ST-specific genes in a TEAD-dependent manner. We also investigated the role of YAP/TAZ-TEAD in maintaining CT cells and their differentiation into ST and EVT cells using human trophoblast stem (TS) cells. YAP/TAZ-TEAD activity was involved in maintaining the stemness of TS cells. Induction or repression of YAP/TAZ-TEAD activity resulted in marked changes in the expression of ST-specific genes. Using primary CT cells, which spontaneously differentiate into ST-like cells, the effects of YAP-5SA transduction were investigated, and the expression of ST-specific genes was found to be repressed. These results indicate that the inhibition of YAP/TAZ-TEAD activity, with or without cAMP stimulation, is essential for the differentiation of CT cells into ST cells.

抑制YAP/TAZ-TEAD活性诱导人滋养细胞向合胞滋养细胞分化。
在胎盘形成过程中,胎盘细胞滋养层细胞(CT)分化为合胞滋养层细胞(ST)和胞外滋养层细胞(EVT)。在胎盘中,Hippo通路通过转录复合体、yes相关蛋白(YAP)/带pdz结合基序的转录辅激活因子(TAZ)-TEA结构域转录因子(TEAD) (YAP/TAZ-TEAD)活性调控各种基因的表达。YAP/TAZ-TEAD活性受多种因素和信号控制,如cAMP信号。cAMP信号被认为参与滋养细胞功能的调节,但尚未完全了解。在人绒毛膜癌细胞系BeWo细胞中,我们发现cAMP刺激改变了YAP/TAZ-TEAD的表达及其活性。YAP/TAZ-TEAD活性的抑制在没有cAMP刺激的情况下诱导了st特异性基因的表达,而组成型活性YAP(即YAP- 5sa)的转导导致8br -cAMP诱导的st特异性基因的表达以依赖于cAMP的方式受到抑制。我们还利用人滋养细胞干细胞研究了YAP/TAZ-TEAD在维持CT细胞并使其分化为ST和EVT细胞中的作用。YAP/TAZ-TEAD活性参与维持TS细胞的干性。诱导或抑制YAP/TAZ-TEAD活性导致st特异性基因的表达发生显著变化。利用自发分化为st样细胞的原代CT细胞,研究了YAP-5SA转导的影响,发现st特异性基因的表达受到抑制。这些结果表明,抑制YAP/TAZ-TEAD活性,无论是否有cAMP刺激,对于CT细胞向ST细胞分化是必不可少的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Molecular human reproduction
Molecular human reproduction 生物-发育生物学
CiteScore
8.30
自引率
0.00%
发文量
37
审稿时长
6-12 weeks
期刊介绍: MHR publishes original research reports, commentaries and reviews on topics in the basic science of reproduction, including: reproductive tract physiology and pathology; gonad function and gametogenesis; fertilization; embryo development; implantation; and pregnancy and parturition. Irrespective of the study subject, research papers should have a mechanistic aspect.
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