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类固醇生成分化和 PKA 信号转导是由肾上腺皮质中的组蛋白甲基转移酶 EZH2 编程的。

Steroidogenic differentiation and PKA signaling are programmed by histone methyltransferase EZH2 in the adrenal cortex.

机构信息

Génétique Reproduction & Développement, CNRS UMR 6293, Inserm U1103, Université Clermont Auvergne, 63001 Clermont-Ferrand, France.

Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892-1103.

出版信息

Proc Natl Acad Sci U S A. 2018 Dec 26;115(52):E12265-E12274. doi: 10.1073/pnas.1809185115. Epub 2018 Dec 12.

Abstract

Adrenal cortex steroids are essential for body homeostasis, and adrenal insufficiency is a life-threatening condition. Adrenal endocrine activity is maintained through recruitment of subcapsular progenitor cells that follow a unidirectional differentiation path from zona glomerulosa to zona fasciculata (zF). Here, we show that this unidirectionality is ensured by the histone methyltransferase EZH2. Indeed, we demonstrate that EZH2 maintains adrenal steroidogenic cell differentiation by preventing expression of GATA4 and WT1 that cause abnormal dedifferentiation to a progenitor-like state in Ezh2 KO adrenals. EZH2 further ensures normal cortical differentiation by programming cells for optimal response to adrenocorticotrophic hormone (ACTH)/PKA signaling. This is achieved by repression of phosphodiesterases PDE1B, 3A, and 7A and of PRKAR1B. Consequently, EZH2 ablation results in blunted zF differentiation and primary glucocorticoid insufficiency. These data demonstrate an all-encompassing role for EZH2 in programming steroidogenic cells for optimal response to differentiation signals and in maintaining their differentiated state.

摘要

肾上腺皮质类固醇对于维持身体内环境稳定至关重要,而肾上腺功能不全是一种危及生命的状况。肾上腺内分泌活动通过募集位于肾上腺被膜下的祖细胞来维持,这些祖细胞沿着从肾小球带到束状带(zF)的单向分化途径分化。在这里,我们表明组蛋白甲基转移酶 EZH2 确保了这种单向性。事实上,我们证明 EZH2 通过防止 GATA4 和 WT1 的表达来维持肾上腺类固醇生成细胞的分化,这会导致 Ezh2 KO 肾上腺中祖细胞样状态的异常去分化。EZH2 还通过为细胞编程以最佳响应促肾上腺皮质激素(ACTH)/PKA 信号来确保正常的皮质分化。这是通过抑制磷酸二酯酶 PDE1B、3A 和 7A 以及 PRKAR1B 来实现的。因此,EZH2 缺失会导致 zF 分化减弱和原发性糖皮质激素不足。这些数据表明 EZH2 在编程类固醇生成细胞以最佳响应分化信号以及维持其分化状态方面发挥着全面的作用。

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