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miR-320 Regulates Glucose-Induced Gene Expression in Diabetes

miRNAs play an important role in several biological processes. Here, we investigated miR-320 in glucose-induced augmented production of vasoactive factors and extracellular matrix (ECM) proteins. High glucose exposure decreased the expression of microRNA 320 (miR-320) but increased the expression of...

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Detalles Bibliográficos
Autores principales: Feng, Biao, Chakrabarti, Subrata
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scholarly Research Network 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3415085/
https://www.ncbi.nlm.nih.gov/pubmed/22900199
http://dx.doi.org/10.5402/2012/549875
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author Feng, Biao
Chakrabarti, Subrata
author_facet Feng, Biao
Chakrabarti, Subrata
author_sort Feng, Biao
collection PubMed
description miRNAs play an important role in several biological processes. Here, we investigated miR-320 in glucose-induced augmented production of vasoactive factors and extracellular matrix (ECM) proteins. High glucose exposure decreased the expression of microRNA 320 (miR-320) but increased the expression of endothelin 1 (ET-1), vascular endothelial growth factor (VEGF), and fibronectin (FN) in human umbilical vein endothelial cells (HUVECs). Transfection of miR-320 mimics restored ET-1, VEGF and FN mRNA, and protein expression in HUVECs treated with high glucose. Furthermore, miR-320 mimic transfection reduced glucose-induced augmented production of ERK1/2. Data from this study indicates that miR-320 negatively regulates expression of ET-1, VEGF, and FN through ERK 1/2. Identification of such novel glucose-induced mechanism regulating gene expression may offer a new strategy for the treatment of diabetic complications.
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spelling pubmed-34150852012-08-16 miR-320 Regulates Glucose-Induced Gene Expression in Diabetes Feng, Biao Chakrabarti, Subrata ISRN Endocrinol Research Article miRNAs play an important role in several biological processes. Here, we investigated miR-320 in glucose-induced augmented production of vasoactive factors and extracellular matrix (ECM) proteins. High glucose exposure decreased the expression of microRNA 320 (miR-320) but increased the expression of endothelin 1 (ET-1), vascular endothelial growth factor (VEGF), and fibronectin (FN) in human umbilical vein endothelial cells (HUVECs). Transfection of miR-320 mimics restored ET-1, VEGF and FN mRNA, and protein expression in HUVECs treated with high glucose. Furthermore, miR-320 mimic transfection reduced glucose-induced augmented production of ERK1/2. Data from this study indicates that miR-320 negatively regulates expression of ET-1, VEGF, and FN through ERK 1/2. Identification of such novel glucose-induced mechanism regulating gene expression may offer a new strategy for the treatment of diabetic complications. International Scholarly Research Network 2012-07-31 /pmc/articles/PMC3415085/ /pubmed/22900199 http://dx.doi.org/10.5402/2012/549875 Text en Copyright © 2012 B. Feng and S. Chakrabarti. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Feng, Biao
Chakrabarti, Subrata
miR-320 Regulates Glucose-Induced Gene Expression in Diabetes
title miR-320 Regulates Glucose-Induced Gene Expression in Diabetes
title_full miR-320 Regulates Glucose-Induced Gene Expression in Diabetes
title_fullStr miR-320 Regulates Glucose-Induced Gene Expression in Diabetes
title_full_unstemmed miR-320 Regulates Glucose-Induced Gene Expression in Diabetes
title_short miR-320 Regulates Glucose-Induced Gene Expression in Diabetes
title_sort mir-320 regulates glucose-induced gene expression in diabetes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3415085/
https://www.ncbi.nlm.nih.gov/pubmed/22900199
http://dx.doi.org/10.5402/2012/549875
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