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Microarray analysis of microRNA expression in bone marrow-derived progenitor cells from mice with type 2 diabetes

Bone-marrow derived vascular precursors are an important endogenous repair reservoir for vascular repair and neovascularization [1]. Therapies of stem/progenitor cells targeting on angiogenesis are considered hopeful solutions for tissue repair and regeneration. However, the dysfunction of patient-d...

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Detalles Bibliográficos
Autores principales: Wang, Jie-Mei, Zhang, Kezhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4778603/
https://www.ncbi.nlm.nih.gov/pubmed/26981370
http://dx.doi.org/10.1016/j.gdata.2015.11.020
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author Wang, Jie-Mei
Zhang, Kezhong
author_facet Wang, Jie-Mei
Zhang, Kezhong
author_sort Wang, Jie-Mei
collection PubMed
description Bone-marrow derived vascular precursors are an important endogenous repair reservoir for vascular repair and neovascularization [1]. Therapies of stem/progenitor cells targeting on angiogenesis are considered hopeful solutions for tissue repair and regeneration. However, the dysfunction of patient-derived progenitor cells has been implicated in diabetes [2], which limited the efficacy of autologous cell therapies in the clinic [3,4]. MicroRNAs are important gene regulators whose functions remain largely unknown. In this project we reported the different microRNA expression profiles in bone marrow-derived progenitor cells from type 2 diabetic mice and their normal controls using microRNA array analysis. All microarray data are available at the Gene Expression Omnibus (GEO) at NCBI (http://www.ncbi.nlm.nih.gov/geo), under accession number GSE72616.
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spelling pubmed-47786032016-03-15 Microarray analysis of microRNA expression in bone marrow-derived progenitor cells from mice with type 2 diabetes Wang, Jie-Mei Zhang, Kezhong Genom Data Data in Brief Bone-marrow derived vascular precursors are an important endogenous repair reservoir for vascular repair and neovascularization [1]. Therapies of stem/progenitor cells targeting on angiogenesis are considered hopeful solutions for tissue repair and regeneration. However, the dysfunction of patient-derived progenitor cells has been implicated in diabetes [2], which limited the efficacy of autologous cell therapies in the clinic [3,4]. MicroRNAs are important gene regulators whose functions remain largely unknown. In this project we reported the different microRNA expression profiles in bone marrow-derived progenitor cells from type 2 diabetic mice and their normal controls using microRNA array analysis. All microarray data are available at the Gene Expression Omnibus (GEO) at NCBI (http://www.ncbi.nlm.nih.gov/geo), under accession number GSE72616. Elsevier 2015-11-23 /pmc/articles/PMC4778603/ /pubmed/26981370 http://dx.doi.org/10.1016/j.gdata.2015.11.020 Text en © 2015 Published by Elsevier Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Data in Brief
Wang, Jie-Mei
Zhang, Kezhong
Microarray analysis of microRNA expression in bone marrow-derived progenitor cells from mice with type 2 diabetes
title Microarray analysis of microRNA expression in bone marrow-derived progenitor cells from mice with type 2 diabetes
title_full Microarray analysis of microRNA expression in bone marrow-derived progenitor cells from mice with type 2 diabetes
title_fullStr Microarray analysis of microRNA expression in bone marrow-derived progenitor cells from mice with type 2 diabetes
title_full_unstemmed Microarray analysis of microRNA expression in bone marrow-derived progenitor cells from mice with type 2 diabetes
title_short Microarray analysis of microRNA expression in bone marrow-derived progenitor cells from mice with type 2 diabetes
title_sort microarray analysis of microrna expression in bone marrow-derived progenitor cells from mice with type 2 diabetes
topic Data in Brief
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4778603/
https://www.ncbi.nlm.nih.gov/pubmed/26981370
http://dx.doi.org/10.1016/j.gdata.2015.11.020
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