Involvement of circRNAs in Proinflammatory Cytokines-Mediated β-Cell Dysfunction

Aim. During the initial stage of type 1 diabetes, prolonged exposure of pancreatic β-cell to proinflammatory cytokines such as IL-1β, TNF-α, and IFN-γ results in a decreased capacity to produce and release insulin, as well as cell loss by apoptosis. Circular RNAs (circRNAs) are a new class of endoge...

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Main Authors: Zhen Wang, Chao Deng, Ying Zheng
Format: Article
Language:English
Published: Wiley 2021-01-01
Series:Mediators of Inflammation
Online Access:http://dx.doi.org/10.1155/2021/5566453
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author Zhen Wang
Chao Deng
Ying Zheng
author_facet Zhen Wang
Chao Deng
Ying Zheng
author_sort Zhen Wang
collection DOAJ
description Aim. During the initial stage of type 1 diabetes, prolonged exposure of pancreatic β-cell to proinflammatory cytokines such as IL-1β, TNF-α, and IFN-γ results in a decreased capacity to produce and release insulin, as well as cell loss by apoptosis. Circular RNAs (circRNAs) are a new class of endogenous noncoding RNAs (ncRNAs) with closed loop with no free ends. circRNAs have been reported to be participated in the development of many diseases. As little is known about their role in insulin-secreting cells, this study is aimed at evaluating their contribution in the process of inflammation-induced β-cell damage. Methods. circRNA expression profile of MIN6 cells stimulated with a mix of cytokines, including IL-1β, IFN-γ, and TNF-α, was detected by circRNA microarrays. Four dysregulated circRNAs were validated by qRT-PCR. The involvement of the selected circRNAs in β-cell dysfunction was tested after their inhibition in MIN6 cells. MicroRNA target prediction software and multiple bioinformatic approaches were used to predict the targeting genes of circRNAs and analyze possible functions of the circRNAs. Results. 1020 upregulated and 902 downregulated circRNAs were identified in cytokines-treated β-cells. Inhibition of circRNAs 000286 and 017277 in β-cells could promote β-cell apoptosis and affect insulin biosynthesis and secretion. GO analysis enriched terms such as regulation of transcription and regulation of gene expression and KEGG analysis enriched top pathways included TGF-β and MAPK signaling pathways. Conclusions. The data shows that circRNAs may be involved in proinflammatory cytokines-mediated β-cell dysfunction and suggests the involvement of circRNAs in the development of type 1 diabetes.
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spelling doaj-art-a5e93561e33541a1911aa029abae3c772025-02-03T06:43:42ZengWileyMediators of Inflammation0962-93511466-18612021-01-01202110.1155/2021/55664535566453Involvement of circRNAs in Proinflammatory Cytokines-Mediated β-Cell DysfunctionZhen Wang0Chao Deng1Ying Zheng2Department of Metabolism and Endocrinology, The Second Xiangya Hospital, Central South University, Changsha, 410011 Hunan, ChinaDepartment of Metabolism and Endocrinology, The Second Xiangya Hospital, Central South University, Changsha, 410011 Hunan, ChinaCenter for Medical Research, The Second Xiangya Hospital, Central South University, Changsha, 410011 Hunan, ChinaAim. During the initial stage of type 1 diabetes, prolonged exposure of pancreatic β-cell to proinflammatory cytokines such as IL-1β, TNF-α, and IFN-γ results in a decreased capacity to produce and release insulin, as well as cell loss by apoptosis. Circular RNAs (circRNAs) are a new class of endogenous noncoding RNAs (ncRNAs) with closed loop with no free ends. circRNAs have been reported to be participated in the development of many diseases. As little is known about their role in insulin-secreting cells, this study is aimed at evaluating their contribution in the process of inflammation-induced β-cell damage. Methods. circRNA expression profile of MIN6 cells stimulated with a mix of cytokines, including IL-1β, IFN-γ, and TNF-α, was detected by circRNA microarrays. Four dysregulated circRNAs were validated by qRT-PCR. The involvement of the selected circRNAs in β-cell dysfunction was tested after their inhibition in MIN6 cells. MicroRNA target prediction software and multiple bioinformatic approaches were used to predict the targeting genes of circRNAs and analyze possible functions of the circRNAs. Results. 1020 upregulated and 902 downregulated circRNAs were identified in cytokines-treated β-cells. Inhibition of circRNAs 000286 and 017277 in β-cells could promote β-cell apoptosis and affect insulin biosynthesis and secretion. GO analysis enriched terms such as regulation of transcription and regulation of gene expression and KEGG analysis enriched top pathways included TGF-β and MAPK signaling pathways. Conclusions. The data shows that circRNAs may be involved in proinflammatory cytokines-mediated β-cell dysfunction and suggests the involvement of circRNAs in the development of type 1 diabetes.http://dx.doi.org/10.1155/2021/5566453
spellingShingle Zhen Wang
Chao Deng
Ying Zheng
Involvement of circRNAs in Proinflammatory Cytokines-Mediated β-Cell Dysfunction
Mediators of Inflammation
title Involvement of circRNAs in Proinflammatory Cytokines-Mediated β-Cell Dysfunction
title_full Involvement of circRNAs in Proinflammatory Cytokines-Mediated β-Cell Dysfunction
title_fullStr Involvement of circRNAs in Proinflammatory Cytokines-Mediated β-Cell Dysfunction
title_full_unstemmed Involvement of circRNAs in Proinflammatory Cytokines-Mediated β-Cell Dysfunction
title_short Involvement of circRNAs in Proinflammatory Cytokines-Mediated β-Cell Dysfunction
title_sort involvement of circrnas in proinflammatory cytokines mediated β cell dysfunction
url http://dx.doi.org/10.1155/2021/5566453
work_keys_str_mv AT zhenwang involvementofcircrnasinproinflammatorycytokinesmediatedbcelldysfunction
AT chaodeng involvementofcircrnasinproinflammatorycytokinesmediatedbcelldysfunction
AT yingzheng involvementofcircrnasinproinflammatorycytokinesmediatedbcelldysfunction