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Sonic hedgehog signaling during adrenal development
Authors:Laufer Ed  Kesper Dörthe  Vortkamp Andrea  King Peter
Affiliation:Department of Pathology and Cell Biology, Columbia University Medical Center, New York, NY 10032, USA. elaufer@columbia.edu
Abstract:It has been speculated for a number of years that Sonic hedgehog (Shh) signaling plays an important role in adrenal development. Over the past two years several reports have described the expression and function of Shh pathway genes in the adrenal cortex, using primarily mouse models. The key findings are that Shh signals produced by a population of partially differentiated cortical cells located in the outer cortex/zona glomerulosa are received by non-cortical mesenchymal cells located predominantly in the overlying capsule. This signal is required for growth of both the capsule and the cortex, but not for cortical zonation or steroidogenic cell differentiation. Using molecular genetic tools to define the adrenocortical cell lineages that are descended from both Shh signaling and receiving cells, both capsule and cortical cells were found to have properties of adrenocortical stem and/or progenitor cells. Here we place these observations within the context of prior studies on adrenal development, postnatal adrenal maintenance and adrenocortical stem/progenitor cell lineages.
Keywords:HPA, hypothalamic–pituitary–adrenal axis   RAS, renin angiotenin system   PHS, Pallister–Hall syndrome   AGP, adrenogonadal primordium   Shh/Ihh/Dhh, Sonic/Indian/Desert hedgehog   Ptch1, patched 1   Smo, smoothened   ZG, zona glomerulosa   ZF, zona fasciculata   POMC, proopiomelanocortin   ACTH, adrenocorticotropic hormone   scc, cholesterol side chain cleavage enzyme, Cyp11a1   Sf-1/Ad4BP, steroidogenic factor-1/adrenal-4-binding protein, NR5A1   TH, tyrosine hydroxylase   GFP/YFP, green/yellow fluorescent protein   LacZ, beta galactosidase   ORF, open reading frame   IRES, internal ribosome entry site   UTR, mRNA untranslated region   dpc, days post coitus
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