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FGF signalling through Fgfr2 isoform IIIb regulates adrenal cortex development

Guasti, L; Candy Sze, WC; McKay, T; Grose, R; King, PJ (2013) FGF signalling through Fgfr2 isoform IIIb regulates adrenal cortex development. MOLECULAR AND CELLULAR ENDOCRINOLOGY, 371 (1-2). 182 - 188. ISSN 0303-7207 https://doi.org/10.1016/j.mce.2013.01.014
SGUL Authors: McKay, Tristan Rowntree

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Abstract

Developmental signalling pathways are implicated in the formation and maintenance of the adrenal gland, but their roles are currently not well defined. In recent years it has emerged that Sonic hedgehog (Shh) and Wnt/β catenin signalling are crucial for the growth and development of the adrenal cortex. Here we demonstrate that Fibroblast growth factor receptor (Fgfr) 2 isoforms IIIb and IIIc are expressed mainly in the adrenal subcapsule during embryogenesis and that specific deletion of the Fgfr2 IIIb isoform impairs adrenal development, causing reduced adrenal growth and impaired expression of SF1 and steroidogenic enzymes. The hypoplastic adrenals also have thicker, disorganised capsules which retain Gli1 expression but no longer express Dlk1. Fgfr2 ligands were detected in both the capsule and the cortex, suggesting the importance of signalling between the capsule and the cortex in adrenal development.

Item Type: Article
Additional Information: Copyright © 2013 Elsevier Ireland Ltd. Open access under CC BY license.
Keywords: Science & Technology, Life Sciences & Biomedicine, Cell Biology, Endocrinology & Metabolism, Adrenal, Development, FGF, FGFR2, Shh, SONIC-HEDGEHOG, TARGETED DISRUPTION, BETA-CATENIN, LIMB BUD, GROWTH, CELLS, RECEPTOR, DIFFERENTIATION, EXPRESSION, PROTEIN
SGUL Research Institute / Research Centre: Academic Structure > Molecular and Clinical Sciences Research Institute (MCS)
Academic Structure > Molecular and Clinical Sciences Research Institute (MCS) > Cell Sciences (INCCCS)
Journal or Publication Title: MOLECULAR AND CELLULAR ENDOCRINOLOGY
ISSN: 0303-7207
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Dates:
DateEvent
22 May 2013Published
Web of Science ID: WOS:000319096600024
Download EPMC Full text (HTML)
URI: https://openaccess.sgul.ac.uk/id/eprint/102367
Publisher's version: https://doi.org/10.1016/j.mce.2013.01.014

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