Functional implications of long non-coding RNAs in the pancreatic islets of Langerhans

Type-2 diabetes (T2D) is a complex disease characterized by insulin resistance in target tissues and impaired insulin release from pancreatic beta cells. As central tissue of glucose homeostasis, the pancreatic islet continues to be an important focus of research to understand the pathophysiology of...

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Main Authors: Lena eEliasson, Jonathan Lou S. Esguerra
Format: Article
Language:English
Published: Frontiers Media S.A. 2014-07-01
Series:Frontiers in Genetics
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fgene.2014.00209/full
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author Lena eEliasson
Jonathan Lou S. Esguerra
author_facet Lena eEliasson
Jonathan Lou S. Esguerra
author_sort Lena eEliasson
collection DOAJ
description Type-2 diabetes (T2D) is a complex disease characterized by insulin resistance in target tissues and impaired insulin release from pancreatic beta cells. As central tissue of glucose homeostasis, the pancreatic islet continues to be an important focus of research to understand the pathophysiology of the disease. The increased access to human pancreatic islets has resulted in improved knowledge of islet function, and together with advances in RNA sequencing and related technologies, revealed the transcriptional and epigenetic landscape of human islet cells. The discovery of thousands of long non-coding RNA (lncRNA) transcripts highly enriched in the pancreatic islet and/or specifically-expressed in the beta-cells, points to yet another layer of gene regulation of many hitherto unknown mechanistic principles governing islet cell functions. Here we review fundamental islet physiology and propose functional implications of the lncRNAs in islet development and endocrine cell functions. We also take into account important differences between rodent and human islets in terms of morphology and function, and suggest how species-specific lncRNAs may partly influence gene regulation to define the unique phenotypic identity of an organism and the functions of its constituent cells. The implication of primate-specific lncRNAs in diabetes will be far-reaching in all aspects of diabetes research, but most importantly in the identification and development of novel targets to improve pancreatic islet cell functions as a therapeutic approach to treat T2D.
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spelling doaj.art-93a8c437b95a4353a21d4a534e3fa3dd2022-12-21T23:34:40ZengFrontiers Media S.A.Frontiers in Genetics1664-80212014-07-01510.3389/fgene.2014.0020998846Functional implications of long non-coding RNAs in the pancreatic islets of LangerhansLena eEliasson0Jonathan Lou S. Esguerra1Lund UniversityLund UniversityType-2 diabetes (T2D) is a complex disease characterized by insulin resistance in target tissues and impaired insulin release from pancreatic beta cells. As central tissue of glucose homeostasis, the pancreatic islet continues to be an important focus of research to understand the pathophysiology of the disease. The increased access to human pancreatic islets has resulted in improved knowledge of islet function, and together with advances in RNA sequencing and related technologies, revealed the transcriptional and epigenetic landscape of human islet cells. The discovery of thousands of long non-coding RNA (lncRNA) transcripts highly enriched in the pancreatic islet and/or specifically-expressed in the beta-cells, points to yet another layer of gene regulation of many hitherto unknown mechanistic principles governing islet cell functions. Here we review fundamental islet physiology and propose functional implications of the lncRNAs in islet development and endocrine cell functions. We also take into account important differences between rodent and human islets in terms of morphology and function, and suggest how species-specific lncRNAs may partly influence gene regulation to define the unique phenotypic identity of an organism and the functions of its constituent cells. The implication of primate-specific lncRNAs in diabetes will be far-reaching in all aspects of diabetes research, but most importantly in the identification and development of novel targets to improve pancreatic islet cell functions as a therapeutic approach to treat T2D.http://journal.frontiersin.org/Journal/10.3389/fgene.2014.00209/fullGlucagonInsulinlong non-coding RNAbeta-cellspancreatic isletstype-2 diabetes
spellingShingle Lena eEliasson
Jonathan Lou S. Esguerra
Functional implications of long non-coding RNAs in the pancreatic islets of Langerhans
Frontiers in Genetics
Glucagon
Insulin
long non-coding RNA
beta-cells
pancreatic islets
type-2 diabetes
title Functional implications of long non-coding RNAs in the pancreatic islets of Langerhans
title_full Functional implications of long non-coding RNAs in the pancreatic islets of Langerhans
title_fullStr Functional implications of long non-coding RNAs in the pancreatic islets of Langerhans
title_full_unstemmed Functional implications of long non-coding RNAs in the pancreatic islets of Langerhans
title_short Functional implications of long non-coding RNAs in the pancreatic islets of Langerhans
title_sort functional implications of long non coding rnas in the pancreatic islets of langerhans
topic Glucagon
Insulin
long non-coding RNA
beta-cells
pancreatic islets
type-2 diabetes
url http://journal.frontiersin.org/Journal/10.3389/fgene.2014.00209/full
work_keys_str_mv AT lenaeeliasson functionalimplicationsoflongnoncodingrnasinthepancreaticisletsoflangerhans
AT jonathanlousesguerra functionalimplicationsoflongnoncodingrnasinthepancreaticisletsoflangerhans