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YAP/TAZ-TEAD 是大鼠颗粒细胞和 KGN 细胞中编码类固醇生成酶的基因的新型转录调节因子。

YAP/TAZ-TEAD is a novel transcriptional regulator of genes encoding steroidogenic enzymes in rat granulosa cells and KGN cells.

机构信息

Department of Nursing, Faculty of Nursing and Welfare Sciences, Fukui Prefectural University, Japan.

Department of Obstetrics and Gynecology, Faculty of Medical Sciences, University of Fukui, Japan.

出版信息

Mol Cell Endocrinol. 2023 Jan 1;559:111808. doi: 10.1016/j.mce.2022.111808. Epub 2022 Oct 26.

Abstract

Steroidogenesis in ovarian granulosa cells is regulated by the follicle-stimulating hormone (FSH) via transcriptional regulation of its related genes. We herein showed the involvement of the Hippo pathway in this regulation. In KGN granulosa cell, repression of YAP/TAZ activity induced the expression of CYP11A1, HSD3B2, and CYP19A1 in a TEAD-dependent manner without cAMP stimulation. A selective inhibitor of p38 MAP kinase, suppressed YAP/TAZ knockdown-indued the expression of these genes, suggesting this signal could be involved. The expression of these genes was induced by 8Br-cAMP, whereas that of CYR61 and ADATS1, typical YAP/TAZ-TEAD target genes, was suppressed, suggesting that the cellular signaling of cAMP reduced YAP/TAZ-TEAD activity. The constitutively active mutant YAP canceled the FSH- and 8Br-cAMP-mediated induction of these genes in primary rat granulosa and KGN cells, respectively. Moreover, regulation of steroidogenesis-related genes by YAP/TAZ-TEAD was independent of steroidogenic factor 1, a master gene regulator of steroidogenesis. These results suggest that YAP/TAZ-TEAD is a negative regulator of steroidogenesis and that suppression of YAP/TAZ-TEAD activity by FSH is involved in ovarian steroidogenesis.

摘要

卵巢颗粒细胞中的类固醇生成受卵泡刺激素 (FSH) 通过其相关基因的转录调控。我们在此表明 Hippo 通路参与了这种调控。在 KGN 颗粒细胞中,YAP/TAZ 活性的抑制以依赖于 TEAD 的方式诱导 CYP11A1、HSD3B2 和 CYP19A1 的表达,而无需 cAMP 刺激。p38 MAP 激酶的选择性抑制剂抑制了 YAP/TAZ 敲低诱导这些基因的表达,表明该信号可能参与其中。这些基因的表达被 8Br-cAMP 诱导,而典型的 YAP/TAZ-TEAD 靶基因 CYR61 和 ADATS1 的表达被抑制,表明 cAMP 的细胞信号降低了 YAP/TAZ-TEAD 活性。组成型激活的突变 YAP 分别取消了 FSH 和 8Br-cAMP 对原代大鼠颗粒细胞和 KGN 细胞中这些基因的介导诱导。此外,YAP/TAZ-TEAD 对类固醇生成相关基因的调节独立于类固醇生成因子 1,后者是类固醇生成的主要基因调节剂。这些结果表明 YAP/TAZ-TEAD 是类固醇生成的负调节剂,FSH 抑制 YAP/TAZ-TEAD 活性参与卵巢类固醇生成。

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