| Literature DB >> 30541888 |
Mickael Mathieu1, Coralie Drelon1, Stéphanie Rodriguez1, Houda Tabbal1, Amandine Septier1, Christelle Damon-Soubeyrand1, Typhanie Dumontet1, Annabel Berthon1,2, Isabelle Sahut-Barnola1, Cyril Djari1, Marie Batisse-Lignier1,3, Jean-Christophe Pointud1, Damien Richard4, Gwenneg Kerdivel5, Marie-Ange Calméjane5, Valentina Boeva5, Igor Tauveron1,3, Anne-Marie Lefrançois-Martinez1, Antoine Martinez1, Pierre Val6.
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.Entities:
Keywords: EZH2; PKA signaling; adrenal; differentiation; progenitors
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Year: 2018 PMID: 30541888 PMCID: PMC6310834 DOI: 10.1073/pnas.1809185115
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205