Insights into β-cell biology and type 2 diabetes pathogenesis from studies of the islet transcriptome

Human β-cells play a pivotal role in the pathogenesis of type 2 diabetes (T2D). Consequently, improved understanding of the molecular and cellular processes critical to the normal function of these cells, and the ways in which these processes are disturbed during disease development, is central to e...

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Main Authors: Van De Bunt, M, Morán, I, Ferrer, J, McCarthy, M
Format: Journal article
Language:English
Published: S. Karger AG 2014
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author Van De Bunt, M
Morán, I
Ferrer, J
McCarthy, M
author_facet Van De Bunt, M
Morán, I
Ferrer, J
McCarthy, M
author_sort Van De Bunt, M
collection OXFORD
description Human β-cells play a pivotal role in the pathogenesis of type 2 diabetes (T2D). Consequently, improved understanding of the molecular and cellular processes critical to the normal function of these cells, and the ways in which these processes are disturbed during disease development, is central to efforts to develop novel therapeutic strategies. Detailed exploration of the transcriptomic, proteomic and metabolomic composition of islet cells provides a platform for defining cellular function. The recent advent of next-generation sequencing approaches is enabling ever more complete inventories of the islet transcriptome, and these data are already providing important insights into islet biology. For example, transcriptome data have contributed to: (a) definition of transcript candidacy at T2D-associated loci; (b) identification of novel disease biomarkers; (c) characterisation of novel regulatory mechanisms (such as those involving non-coding RNAs), and (d) discovery of factors of potential relevance to β-cell reprogramming efforts.
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spelling oxford-uuid:ab07193f-745c-4750-b1b5-ee36b571b2652022-03-27T03:19:15ZInsights into β-cell biology and type 2 diabetes pathogenesis from studies of the islet transcriptomeJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:ab07193f-745c-4750-b1b5-ee36b571b265EnglishSymplectic Elements at OxfordS. Karger AG2014Van De Bunt, MMorán, IFerrer, JMcCarthy, MHuman β-cells play a pivotal role in the pathogenesis of type 2 diabetes (T2D). Consequently, improved understanding of the molecular and cellular processes critical to the normal function of these cells, and the ways in which these processes are disturbed during disease development, is central to efforts to develop novel therapeutic strategies. Detailed exploration of the transcriptomic, proteomic and metabolomic composition of islet cells provides a platform for defining cellular function. The recent advent of next-generation sequencing approaches is enabling ever more complete inventories of the islet transcriptome, and these data are already providing important insights into islet biology. For example, transcriptome data have contributed to: (a) definition of transcript candidacy at T2D-associated loci; (b) identification of novel disease biomarkers; (c) characterisation of novel regulatory mechanisms (such as those involving non-coding RNAs), and (d) discovery of factors of potential relevance to β-cell reprogramming efforts.
spellingShingle Van De Bunt, M
Morán, I
Ferrer, J
McCarthy, M
Insights into β-cell biology and type 2 diabetes pathogenesis from studies of the islet transcriptome
title Insights into β-cell biology and type 2 diabetes pathogenesis from studies of the islet transcriptome
title_full Insights into β-cell biology and type 2 diabetes pathogenesis from studies of the islet transcriptome
title_fullStr Insights into β-cell biology and type 2 diabetes pathogenesis from studies of the islet transcriptome
title_full_unstemmed Insights into β-cell biology and type 2 diabetes pathogenesis from studies of the islet transcriptome
title_short Insights into β-cell biology and type 2 diabetes pathogenesis from studies of the islet transcriptome
title_sort insights into β cell biology and type 2 diabetes pathogenesis from studies of the islet transcriptome
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AT mccarthym insightsintobcellbiologyandtype2diabetespathogenesisfromstudiesoftheislettranscriptome