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      Adrenocortical Zonation, Renewal, and Remodeling

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          Abstract

          The adrenal cortex is divided into concentric zones. In humans the major cortical zones are the zona glomerulosa, zona fasciculata, and zona reticularis. The adrenal cortex is a dynamic organ in which senescent cells are replaced by newly differentiated ones. This constant renewal facilitates organ remodeling in response to physiological demand for steroids. Cortical zones can reversibly expand, contract, or alter their biochemical profiles to accommodate needs. Pools of stem/progenitor cells in the adrenal capsule, subcapsular region, and juxtamedullary region can differentiate to repopulate or expand zones. Some of these pools appear to be activated only during specific developmental windows or in response to extreme physiological demand. Senescent cells can also be replenished through direct lineage conversion; for example, cells in the zona glomerulosa can transform into cells of the zona fasciculata. Adrenocortical cell differentiation, renewal, and function are regulated by a variety of endocrine/paracrine factors including adrenocorticotropin, angiotensin II, insulin-related growth hormones, luteinizing hormone, activin, and inhibin. Additionally, zonation and regeneration of the adrenal cortex are controlled by developmental signaling pathways, such as the sonic hedgehog, delta-like homolog 1, fibroblast growth factor, and WNT/β-catenin pathways. The mechanisms involved in adrenocortical remodeling are complex and redundant so as to fulfill the offsetting goals of organ homeostasis and stress adaptation.

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          Most cited references99

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          Integrated genomic characterization of adrenocortical carcinoma.

          Adrenocortical carcinomas (ACCs) are aggressive cancers originating in the cortex of the adrenal gland. Despite overall poor prognosis, ACC outcome is heterogeneous. We performed exome sequencing and SNP array analysis of 45 ACCs and identified recurrent alterations in known driver genes (CTNNB1, TP53, CDKN2A, RB1 and MEN1) and in genes not previously reported in ACC (ZNRF3, DAXX, TERT and MED12), which we validated in an independent cohort of 77 ACCs. ZNRF3, encoding a cell surface E3 ubiquitin ligase, was the most frequently altered gene (21%) and is a potential new tumor suppressor gene related to the β-catenin pathway. Our integrated genomic analyses further identified two distinct molecular subgroups with opposite outcome. The C1A group of ACCs with poor outcome displayed numerous mutations and DNA methylation alterations, whereas the C1B group of ACCs with good prognosis displayed specific deregulation of two microRNA clusters. Thus, aggressive and indolent ACCs correspond to two distinct molecular entities driven by different oncogenic alterations.
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            A Gata6-Wnt pathway required for epithelial stem cell development and airway regeneration.

            Epithelial organs, including the lung, are known to possess regenerative abilities through activation of endogenous stem cell populations, but the molecular pathways regulating stem cell expansion and regeneration are not well understood. Here we show that Gata6 regulates the temporal appearance and number of bronchioalveolar stem cells (BASCs) in the lung, its absence in Gata6-null lung epithelium leading to the precocious appearance of BASCs and concurrent loss in epithelial differentiation. This expansion of BASCs was the result of a pronounced increase in canonical Wnt signaling in lung epithelium upon loss of Gata6. Expression of the noncanonical Wnt receptor Fzd2 was downregulated in Gata6 mutants and increased Fzd2 or decreased beta-catenin expression rescued, in part, the lung epithelial defects in Gata6 mutants. During lung epithelial regeneration, canonical Wnt signaling was activated in the niche containing BASCs and forced activation of Wnt signaling led to a large increase in BASC numbers. Moreover, Gata6 was required for proper lung epithelial regeneration, and postnatal loss of Gata6 led to increased BASC expansion and decreased differentiation. Together, these data demonstrate that Gata6-regulated Wnt signaling controls the balance between progenitor expansion and epithelial differentiation required for both lung development and regeneration.
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              Constitutive beta-catenin activation induces adrenal hyperplasia and promotes adrenal cancer development.

              Adrenocortical carcinoma is a rare but aggressive cancer with unknown aetiology. Constitutive activation of beta-catenin is the most frequent alteration in benign and malignant adrenocortical tumours in patients. Here, we show that constitutive activation of beta-catenin in the adrenal cortex of transgenic mice resulted in progressive steroidogenic and undifferentiated spindle-shaped cells hyperplasia as well as dysplasia of the cortex and medulla. Over a 17 months time course, transgenic adrenals developed malignant characteristics such as uncontrolled neovascularization and loco-regional metastatic invasion. These oncogenic events were accompanied by ectopic differentiation of glomerulosa at the expense of fasciculata cells, which caused primary hyperaldosteronism. Altogether these observations demonstrate that constitutively active beta-catenin is an adrenal oncogene which triggers benign aldosterone-secreting tumour development and promotes malignancy.
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                Author and article information

                Contributors
                URI : http://frontiersin.org/people/u/207281
                URI : http://frontiersin.org/people/u/203282
                URI : http://frontiersin.org/people/u/181055
                Journal
                Front Endocrinol (Lausanne)
                Front Endocrinol (Lausanne)
                Front. Endocrinol.
                Frontiers in Endocrinology
                Frontiers Media S.A.
                1664-2392
                05 March 2015
                2015
                : 6
                : 27
                Affiliations
                [1] 1Helsinki University Central Hospital, Children’s Hospital, University of Helsinki , Helsinki, Finland
                [2] 2Hochschule Mannheim – University of Applied Sciences , Mannheim, Germany
                [3] 3St. Louis Children’s Hospital, Washington University School of Medicine , St. Louis, MO, USA
                Author notes

                Edited by: Pierre Val, Centre National de la Recherche Scientifique, France

                Reviewed by: David Breault, Boston Children’s Hospital, USA; Gary Hammer, University of Michigan, USA

                *Correspondence: David B. Wilson, Washington University School of Medicine, Box 8208, 660 South Euclid Avenue, St. Louis, MO 63110, USA e-mail: wilson_d@ 123456wustl.edu

                This article was submitted to Cellular Endocrinology, a section of the journal Frontiers in Endocrinology.

                Article
                10.3389/fendo.2015.00027
                4350438
                25798129
                821b5c39-24f7-4a1d-b62e-8de09ca0f97f
                Copyright © 2015 Pihlajoki, Dörner, Cochran, Heikinheimo and Wilson.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 18 December 2014
                : 16 February 2015
                Page count
                Figures: 10, Tables: 5, Equations: 0, References: 114, Pages: 14, Words: 10582
                Funding
                Funded by: American Heart Association
                Award ID: 13GRNT16850031
                Funded by: DOD
                Award ID: PC141008
                Funded by: NIH
                Award ID: DK52574
                Funded by: Washington University, Sigrid Jusélius Foundation
                Funded by: Academy of Finland
                Categories
                Endocrinology
                Review Article

                Endocrinology & Diabetes
                adrenal cortex,hormone,plasticity,stem cell,steroid,steroidogenesis
                Endocrinology & Diabetes
                adrenal cortex, hormone, plasticity, stem cell, steroid, steroidogenesis

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