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Regulation of PPAR[gamma] and CIDEC expression by adenovirus 36 in adipocyte differentiation

This study is to investigate the role of adenovirus 36 (Ad36) in regulating expression of peroxisome proliferator-activated receptor [gamma] (PPAR[gamma]) and cell death-inducing DFFA-like effector c (CIDEC) in Ad36-induced adipocyte differentiation. Human adipose-derived mesenchymal stem cells (hAM...

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Published in:Molecular and cellular biochemistry 2017-04, Vol.428 (1-2), p.1
Main Authors: Jiao, Yi, Aisa, Yiliyasi, Liang, Xiaodi, Nuermaimaiti, Nuerbiye, Gong, Xian, Zhang, Zhaoxia, Guan, Yaqun
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container_title Molecular and cellular biochemistry
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Aisa, Yiliyasi
Liang, Xiaodi
Nuermaimaiti, Nuerbiye
Gong, Xian
Zhang, Zhaoxia
Guan, Yaqun
description This study is to investigate the role of adenovirus 36 (Ad36) in regulating expression of peroxisome proliferator-activated receptor [gamma] (PPAR[gamma]) and cell death-inducing DFFA-like effector c (CIDEC) in Ad36-induced adipocyte differentiation. Human adipose-derived mesenchymal stem cells (hAMSCs) were isolated and cultured, and then infected with Ad36. Ad36-induced adipocytes were identified using quantitative real-time PCR and Oil red O staining. The expression levels of PPAR[gamma] and CIDEC in Ad36-induced adipocytes were determined by quantitative real-time PCR and Western blot analysis. Glucose uptake and intracellular triglyceride content were also determined in these induced cells. Our results from the Oil red O staining showed that Ad36 induced the differentiation of hAMSCs into human adipocytes in vitro. Moreover, the medium glucose concentration was significantly decreased, while the intracellular triglyceride content was significantly increased, in the Ad36-induced adipocytes, compared with the control group. Furthermore, our results showed that, the mRNA and protein expression levels of PPAR[gamma] and CIDEC were significantly upregulated in Ad36-induced adipocytes, in a time-dependent manner. On the other hand, compared with the control group, the CIDEC expression was downregulated when the Ad36-induced adipocytes were treated with the PPAR[gamma] inhibitor, GW9662. Ad36 could upregulate the expression level of CIDEC through increasing PPAR[gamma] expression during the adipocyte differentiation process.
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Human adipose-derived mesenchymal stem cells (hAMSCs) were isolated and cultured, and then infected with Ad36. Ad36-induced adipocytes were identified using quantitative real-time PCR and Oil red O staining. The expression levels of PPAR[gamma] and CIDEC in Ad36-induced adipocytes were determined by quantitative real-time PCR and Western blot analysis. Glucose uptake and intracellular triglyceride content were also determined in these induced cells. Our results from the Oil red O staining showed that Ad36 induced the differentiation of hAMSCs into human adipocytes in vitro. Moreover, the medium glucose concentration was significantly decreased, while the intracellular triglyceride content was significantly increased, in the Ad36-induced adipocytes, compared with the control group. Furthermore, our results showed that, the mRNA and protein expression levels of PPAR[gamma] and CIDEC were significantly upregulated in Ad36-induced adipocytes, in a time-dependent manner. 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subjects Adenoviruses
Adipocytes
Cell death
Glucose
Glucose metabolism
Protein expression
RNA
Stem cells
Triglycerides
title Regulation of PPAR[gamma] and CIDEC expression by adenovirus 36 in adipocyte differentiation
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