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The diabetes gene Hhex maintains δ-cell differentiation and islet function

The homeodomain transcription factor HHEX (hematopoietically expressed homeobox) has been repeatedly linked to type 2 diabetes mellitus (T2DM) using genome-wide association studies. We report here that within the adult endocrine pancreas, Hhex is selectively expressed in the somatostatin-secreting δ...

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Detalles Bibliográficos
Autores principales: Zhang, Jia, McKenna, Lindsay B., Bogue, Clifford W., Kaestner, Klaus H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4003275/
https://www.ncbi.nlm.nih.gov/pubmed/24736842
http://dx.doi.org/10.1101/gad.235499.113
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author Zhang, Jia
McKenna, Lindsay B.
Bogue, Clifford W.
Kaestner, Klaus H.
author_facet Zhang, Jia
McKenna, Lindsay B.
Bogue, Clifford W.
Kaestner, Klaus H.
author_sort Zhang, Jia
collection PubMed
description The homeodomain transcription factor HHEX (hematopoietically expressed homeobox) has been repeatedly linked to type 2 diabetes mellitus (T2DM) using genome-wide association studies. We report here that within the adult endocrine pancreas, Hhex is selectively expressed in the somatostatin-secreting δ cell. Using two mouse models with Hhex deficiency in the endocrine pancreas, we show that Hhex is required for δ-cell differentiation. Decreased somatostatin levels in Hhex-deficient islets cause disrupted paracrine inhibition of insulin release from β cells. These findings identify Hhex as the first transcriptional regulator specifically required for islet δ cells and suggest compromised paracrine control as a contributor to T2DM.
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spelling pubmed-40032752014-10-15 The diabetes gene Hhex maintains δ-cell differentiation and islet function Zhang, Jia McKenna, Lindsay B. Bogue, Clifford W. Kaestner, Klaus H. Genes Dev Research Communication The homeodomain transcription factor HHEX (hematopoietically expressed homeobox) has been repeatedly linked to type 2 diabetes mellitus (T2DM) using genome-wide association studies. We report here that within the adult endocrine pancreas, Hhex is selectively expressed in the somatostatin-secreting δ cell. Using two mouse models with Hhex deficiency in the endocrine pancreas, we show that Hhex is required for δ-cell differentiation. Decreased somatostatin levels in Hhex-deficient islets cause disrupted paracrine inhibition of insulin release from β cells. These findings identify Hhex as the first transcriptional regulator specifically required for islet δ cells and suggest compromised paracrine control as a contributor to T2DM. Cold Spring Harbor Laboratory Press 2014-04-15 /pmc/articles/PMC4003275/ /pubmed/24736842 http://dx.doi.org/10.1101/gad.235499.113 Text en © 2014 Zhang et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genesdev.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Research Communication
Zhang, Jia
McKenna, Lindsay B.
Bogue, Clifford W.
Kaestner, Klaus H.
The diabetes gene Hhex maintains δ-cell differentiation and islet function
title The diabetes gene Hhex maintains δ-cell differentiation and islet function
title_full The diabetes gene Hhex maintains δ-cell differentiation and islet function
title_fullStr The diabetes gene Hhex maintains δ-cell differentiation and islet function
title_full_unstemmed The diabetes gene Hhex maintains δ-cell differentiation and islet function
title_short The diabetes gene Hhex maintains δ-cell differentiation and islet function
title_sort diabetes gene hhex maintains δ-cell differentiation and islet function
topic Research Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4003275/
https://www.ncbi.nlm.nih.gov/pubmed/24736842
http://dx.doi.org/10.1101/gad.235499.113
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