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PKA 信号驱动网状细胞分化和性别二态性肾上腺皮质更新。

PKA signaling drives reticularis differentiation and sexually dimorphic adrenal cortex renewal.

机构信息

GReD, Université Clermont Auvergne, CNRS, INSERM, Clermont-Ferrand, France.

Molecular Endocrinology and Rare Diseases, University Hospital, Claude Bernard Lyon 1 University, Bron, France.

出版信息

JCI Insight. 2018 Jan 25;3(2). doi: 10.1172/jci.insight.98394.

Abstract

The adrenal cortex undergoes remodeling during fetal and postnatal life. How zona reticularis emerges in the postnatal gland to support adrenarche, a process whereby higher primates increase prepubertal androgen secretion, is unknown. Using cell-fate mapping and gene deletion studies in mice, we show that activation of PKA has no effect on the fetal cortex, while it accelerates regeneration of the adult cortex, triggers zona fasciculata differentiation that is subsequently converted into a functional reticularis-like zone, and drives hypersecretion syndromes. Remarkably, PKA effects are influenced by sex. Indeed, testicular androgens increase WNT signaling that antagonizes PKA, leading to slower adrenocortical cell turnover and delayed phenotype whereas gonadectomy sensitizes males to hypercorticism and reticularis-like formation. Thus, reticularis results from ultimate centripetal conversion of adult cortex under the combined effects of PKA and cell turnover that dictate organ size. We show that PKA-induced progenitor recruitment is sexually dimorphic and may provide a paradigm for overrepresentation of women in adrenal diseases.

摘要

肾上腺皮质在胎儿期和出生后经历重塑。尚不清楚在出生后的腺体中,网状带如何出现以支持肾上腺皮质功能亢进,这是一种更高等灵长类动物增加青春期前雄激素分泌的过程。通过对小鼠的细胞谱系追踪和基因缺失研究,我们发现 PKA 的激活对胎儿皮质没有影响,而它加速了成年皮质的再生,触发了带细胞的分化,随后转化为具有功能的网状带样区域,并导致过度分泌综合征。值得注意的是,PKA 的作用受到性别的影响。事实上,睾丸雄激素增加 WNT 信号,拮抗 PKA,导致肾上腺皮质细胞更替速度减慢和表型延迟,而性腺切除术使雄性对皮质醇过多和网状带样形成更为敏感。因此,网状带是在 PKA 和细胞更替的综合作用下,从成年皮质的最终向心性转化而来的,这决定了器官的大小。我们表明,PKA 诱导的祖细胞募集存在性别二态性,可能为女性在肾上腺疾病中过度出现提供了一个范例。

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