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MicroRNA Expression in Human Omental and Subcutaneous Adipose Tissue

MicroRNAs (miRNAs) are small non-coding RNAs, that play important regulatory roles in a variety of biological processes, including development, differentiation, apoptosis, and metabolism. In mammals, miRNAs have been shown to modulate adipocyte differentiation. Therefore, we performed a global miRNA...

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Autores principales: Klöting, Nora, Berthold, Susan, Kovacs, Peter, Schön, Michael R., Fasshauer, Mathias, Ruschke, Karen, Stumvoll, Michael, Blüher, Matthias
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2649537/
https://www.ncbi.nlm.nih.gov/pubmed/19259271
http://dx.doi.org/10.1371/journal.pone.0004699
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author Klöting, Nora
Berthold, Susan
Kovacs, Peter
Schön, Michael R.
Fasshauer, Mathias
Ruschke, Karen
Stumvoll, Michael
Blüher, Matthias
author_facet Klöting, Nora
Berthold, Susan
Kovacs, Peter
Schön, Michael R.
Fasshauer, Mathias
Ruschke, Karen
Stumvoll, Michael
Blüher, Matthias
author_sort Klöting, Nora
collection PubMed
description MicroRNAs (miRNAs) are small non-coding RNAs, that play important regulatory roles in a variety of biological processes, including development, differentiation, apoptosis, and metabolism. In mammals, miRNAs have been shown to modulate adipocyte differentiation. Therefore, we performed a global miRNA gene expression assay in different fat depots of overweight and obese individuals to investigate whether miRNA expression in human adipose tissue is fat-depot specific and associated with parameters of obesity and glucose metabolism. Paired samples of abdominal subcutaneous (SC) and intraabdominal omental adipose tissue were obtained from fifteen individuals with either normal glucose tolerance (NGT, n = 9) or newly diagnosed type 2 diabetes (T2D, n = 6). Expression of 155 miRNAs was carried out using the TaqMan®MicroRNA Assays Human Panel Early Access Kit (Applied Biosystems, Darmstadt, Germany). We identified expression of 106 (68%) miRNAs in human omental and SC adipose tissue. There was no miRNA exclusively expressed in either fat depot, suggesting common developmental origin of both fat depots. Sixteen miRNAs (4 in NGT, 12 in T2D group) showed a significant fat depot specific expression pattern. We identified significant correlations between the expression of miRNA-17-5p, -132, -99a, -134, 181a, -145, -197 and both adipose tissue morphology and key metabolic parameters, including visceral fat area, HbA(1c), fasting plasma glucose, and circulating leptin, adiponectin, interleukin-6. In conclusion, microRNA expression differences may contribute to intrinsic differences between omental and subcutaneous adipose tissue. In addition, human adipose tissue miRNA expression correlates with adipocyte phenotype, parameters of obesity and glucose metabolism.
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spelling pubmed-26495372009-03-04 MicroRNA Expression in Human Omental and Subcutaneous Adipose Tissue Klöting, Nora Berthold, Susan Kovacs, Peter Schön, Michael R. Fasshauer, Mathias Ruschke, Karen Stumvoll, Michael Blüher, Matthias PLoS One Research Article MicroRNAs (miRNAs) are small non-coding RNAs, that play important regulatory roles in a variety of biological processes, including development, differentiation, apoptosis, and metabolism. In mammals, miRNAs have been shown to modulate adipocyte differentiation. Therefore, we performed a global miRNA gene expression assay in different fat depots of overweight and obese individuals to investigate whether miRNA expression in human adipose tissue is fat-depot specific and associated with parameters of obesity and glucose metabolism. Paired samples of abdominal subcutaneous (SC) and intraabdominal omental adipose tissue were obtained from fifteen individuals with either normal glucose tolerance (NGT, n = 9) or newly diagnosed type 2 diabetes (T2D, n = 6). Expression of 155 miRNAs was carried out using the TaqMan®MicroRNA Assays Human Panel Early Access Kit (Applied Biosystems, Darmstadt, Germany). We identified expression of 106 (68%) miRNAs in human omental and SC adipose tissue. There was no miRNA exclusively expressed in either fat depot, suggesting common developmental origin of both fat depots. Sixteen miRNAs (4 in NGT, 12 in T2D group) showed a significant fat depot specific expression pattern. We identified significant correlations between the expression of miRNA-17-5p, -132, -99a, -134, 181a, -145, -197 and both adipose tissue morphology and key metabolic parameters, including visceral fat area, HbA(1c), fasting plasma glucose, and circulating leptin, adiponectin, interleukin-6. In conclusion, microRNA expression differences may contribute to intrinsic differences between omental and subcutaneous adipose tissue. In addition, human adipose tissue miRNA expression correlates with adipocyte phenotype, parameters of obesity and glucose metabolism. Public Library of Science 2009-03-04 /pmc/articles/PMC2649537/ /pubmed/19259271 http://dx.doi.org/10.1371/journal.pone.0004699 Text en Klöting et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Klöting, Nora
Berthold, Susan
Kovacs, Peter
Schön, Michael R.
Fasshauer, Mathias
Ruschke, Karen
Stumvoll, Michael
Blüher, Matthias
MicroRNA Expression in Human Omental and Subcutaneous Adipose Tissue
title MicroRNA Expression in Human Omental and Subcutaneous Adipose Tissue
title_full MicroRNA Expression in Human Omental and Subcutaneous Adipose Tissue
title_fullStr MicroRNA Expression in Human Omental and Subcutaneous Adipose Tissue
title_full_unstemmed MicroRNA Expression in Human Omental and Subcutaneous Adipose Tissue
title_short MicroRNA Expression in Human Omental and Subcutaneous Adipose Tissue
title_sort microrna expression in human omental and subcutaneous adipose tissue
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2649537/
https://www.ncbi.nlm.nih.gov/pubmed/19259271
http://dx.doi.org/10.1371/journal.pone.0004699
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