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MicroRNA-378 Regulates Adiponectin Expression in Adipose Tissue: A New Plausible Mechanism

AIMS: Mechanisms regulating adiponectin expression have not been fully clarified. MicroRNAs (miRNAs), small non-coding RNAs that regulate gene expression, are involved in biological processes, including obesity and insulin resistance. We evaluated whether the miRNA-378 pathway is involved in regulat...

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Autores principales: Ishida, Masayoshi, Shimabukuro, Michio, Yagi, Shusuke, Nishimoto, Sachiko, Kozuka, Chisayo, Fukuda, Daiju, Soeki, Takeshi, Masuzaki, Hiroaki, Tsutsui, Masato, Sata, Masataka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4224402/
https://www.ncbi.nlm.nih.gov/pubmed/25379946
http://dx.doi.org/10.1371/journal.pone.0111537
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author Ishida, Masayoshi
Shimabukuro, Michio
Yagi, Shusuke
Nishimoto, Sachiko
Kozuka, Chisayo
Fukuda, Daiju
Soeki, Takeshi
Masuzaki, Hiroaki
Tsutsui, Masato
Sata, Masataka
author_facet Ishida, Masayoshi
Shimabukuro, Michio
Yagi, Shusuke
Nishimoto, Sachiko
Kozuka, Chisayo
Fukuda, Daiju
Soeki, Takeshi
Masuzaki, Hiroaki
Tsutsui, Masato
Sata, Masataka
author_sort Ishida, Masayoshi
collection PubMed
description AIMS: Mechanisms regulating adiponectin expression have not been fully clarified. MicroRNAs (miRNAs), small non-coding RNAs that regulate gene expression, are involved in biological processes, including obesity and insulin resistance. We evaluated whether the miRNA-378 pathway is involved in regulating adiponectin expression. METHODS AND RESULTS: First, we determined a putative target site for miRNA-378 in the 3 prime untranslated region (3'UTR) of the adiponectin gene by in silico analysis. The levels of adiponectin mRNA and protein were decreased in 3T3-L1 cells overexpressing the mimic of miRNA-378. Luminescence activity in HEK293T cells expressing a renilla-luciferase-adiponectin-3'UTR sequence was inhibited by overexpressing the mimic of miRNA-378, and the decrease was reversed by adding the inhibitor of miRNA-378. Moreover, we confirmed the inhibitory effects of the mimic were cancelled in a deleted mutant of the miR-378 3′-UTR binding site. Addition of tumor necrosis factor-α (TNFα) led a upregulation of miR-378 and downregulation of adiponectin at mRNA and protein levels in 3T3-L1 cells. Level of miR-378 was higher and mRNA level of adiponectin was lower in diabetic ob/ob mice than those of normal C57BL/6 mice and levels of miR378 and adiponectin were negatively well correlated (r = −0.624, p = 0.004). CONCLUSIONS: We found that levels of miRNA-378 could modulate adiponectin expression via the 3'UTR sequence-binding site. Our findings warrant further investigations into the role of miRNAs in regulating the adiponectin expression.
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spelling pubmed-42244022014-11-18 MicroRNA-378 Regulates Adiponectin Expression in Adipose Tissue: A New Plausible Mechanism Ishida, Masayoshi Shimabukuro, Michio Yagi, Shusuke Nishimoto, Sachiko Kozuka, Chisayo Fukuda, Daiju Soeki, Takeshi Masuzaki, Hiroaki Tsutsui, Masato Sata, Masataka PLoS One Research Article AIMS: Mechanisms regulating adiponectin expression have not been fully clarified. MicroRNAs (miRNAs), small non-coding RNAs that regulate gene expression, are involved in biological processes, including obesity and insulin resistance. We evaluated whether the miRNA-378 pathway is involved in regulating adiponectin expression. METHODS AND RESULTS: First, we determined a putative target site for miRNA-378 in the 3 prime untranslated region (3'UTR) of the adiponectin gene by in silico analysis. The levels of adiponectin mRNA and protein were decreased in 3T3-L1 cells overexpressing the mimic of miRNA-378. Luminescence activity in HEK293T cells expressing a renilla-luciferase-adiponectin-3'UTR sequence was inhibited by overexpressing the mimic of miRNA-378, and the decrease was reversed by adding the inhibitor of miRNA-378. Moreover, we confirmed the inhibitory effects of the mimic were cancelled in a deleted mutant of the miR-378 3′-UTR binding site. Addition of tumor necrosis factor-α (TNFα) led a upregulation of miR-378 and downregulation of adiponectin at mRNA and protein levels in 3T3-L1 cells. Level of miR-378 was higher and mRNA level of adiponectin was lower in diabetic ob/ob mice than those of normal C57BL/6 mice and levels of miR378 and adiponectin were negatively well correlated (r = −0.624, p = 0.004). CONCLUSIONS: We found that levels of miRNA-378 could modulate adiponectin expression via the 3'UTR sequence-binding site. Our findings warrant further investigations into the role of miRNAs in regulating the adiponectin expression. Public Library of Science 2014-11-07 /pmc/articles/PMC4224402/ /pubmed/25379946 http://dx.doi.org/10.1371/journal.pone.0111537 Text en © 2014 Ishida 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
Ishida, Masayoshi
Shimabukuro, Michio
Yagi, Shusuke
Nishimoto, Sachiko
Kozuka, Chisayo
Fukuda, Daiju
Soeki, Takeshi
Masuzaki, Hiroaki
Tsutsui, Masato
Sata, Masataka
MicroRNA-378 Regulates Adiponectin Expression in Adipose Tissue: A New Plausible Mechanism
title MicroRNA-378 Regulates Adiponectin Expression in Adipose Tissue: A New Plausible Mechanism
title_full MicroRNA-378 Regulates Adiponectin Expression in Adipose Tissue: A New Plausible Mechanism
title_fullStr MicroRNA-378 Regulates Adiponectin Expression in Adipose Tissue: A New Plausible Mechanism
title_full_unstemmed MicroRNA-378 Regulates Adiponectin Expression in Adipose Tissue: A New Plausible Mechanism
title_short MicroRNA-378 Regulates Adiponectin Expression in Adipose Tissue: A New Plausible Mechanism
title_sort microrna-378 regulates adiponectin expression in adipose tissue: a new plausible mechanism
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4224402/
https://www.ncbi.nlm.nih.gov/pubmed/25379946
http://dx.doi.org/10.1371/journal.pone.0111537
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