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Knockdown of LXRα Inhibits Goat Intramuscular Preadipocyte Differentiation

Goat intramuscular fat (IMF) content is mainly determined by the processes of intramuscular preadipocytes adipogenic differentiation and mature adipocyte lipid accumulation. However, the underlying regulators of these biological processes remain largely unknown. Here, we report that the expression o...

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Autores principales: Xiong, Yan, Xu, Qing, Lin, Sen, Wang, Yong, Lin, Yaqiu, Zhu, Jiangjiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6213902/
https://www.ncbi.nlm.nih.gov/pubmed/30301149
http://dx.doi.org/10.3390/ijms19103037
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author Xiong, Yan
Xu, Qing
Lin, Sen
Wang, Yong
Lin, Yaqiu
Zhu, Jiangjiang
author_facet Xiong, Yan
Xu, Qing
Lin, Sen
Wang, Yong
Lin, Yaqiu
Zhu, Jiangjiang
author_sort Xiong, Yan
collection PubMed
description Goat intramuscular fat (IMF) content is mainly determined by the processes of intramuscular preadipocytes adipogenic differentiation and mature adipocyte lipid accumulation. However, the underlying regulators of these biological processes remain largely unknown. Here, we report that the expression of Liver X receptor alpha (LXRα) reaches a peak at early stage and then gradually decreases during goat intramuscular adipogenesis. Knockdown of LXRα mediated by two independent siRNAs significantly inhibits intramuscular adipocytes lipid accumulation and upregulates preadipocytes marker- preadipocyte factor 1 (pref1) expression. Consistently, siRNA treatments robustly decrease mRNA level of adipogenic related genes, including CCAAT enhancer binding protein alpha (Cebpα), Peroxisome proliferator activated receptor gamma (Pparg), Sterol regulatory element binding protein isoform 1c (Srebp1c), Fatty acids binding protein (aP2) and Lipoprotein lipase (Lpl). Next, adenovirus overexpression of LXRα does not affect intramuscular adipocytes adipogenesis manifested by Oil Red O signal measurement and adipogenic specific genes detection. Mechanically, we found that both CCAAT enhancer binding protein beta (Cebpβ) and Kruppel like factor 8 (Klf8) are potential targets of LXRα, indicated by having putative binding sites of LXRα at the promoter of these genes and similar expression pattern during adipogenesis comparing to LXRα. Importantly, mRNA levels of Cebpβ and Klf8 are downregulated significantly in goat LXRα knockdown intramuscular adipocyte. These results demonstrate that loss function of LXRα inhibits intramuscular adipogenesis possibly through down-regulation of Cebpβ and Klf8. Our research will provide new insights into mechanical regulation of goat IMF deposition.
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spelling pubmed-62139022018-11-14 Knockdown of LXRα Inhibits Goat Intramuscular Preadipocyte Differentiation Xiong, Yan Xu, Qing Lin, Sen Wang, Yong Lin, Yaqiu Zhu, Jiangjiang Int J Mol Sci Article Goat intramuscular fat (IMF) content is mainly determined by the processes of intramuscular preadipocytes adipogenic differentiation and mature adipocyte lipid accumulation. However, the underlying regulators of these biological processes remain largely unknown. Here, we report that the expression of Liver X receptor alpha (LXRα) reaches a peak at early stage and then gradually decreases during goat intramuscular adipogenesis. Knockdown of LXRα mediated by two independent siRNAs significantly inhibits intramuscular adipocytes lipid accumulation and upregulates preadipocytes marker- preadipocyte factor 1 (pref1) expression. Consistently, siRNA treatments robustly decrease mRNA level of adipogenic related genes, including CCAAT enhancer binding protein alpha (Cebpα), Peroxisome proliferator activated receptor gamma (Pparg), Sterol regulatory element binding protein isoform 1c (Srebp1c), Fatty acids binding protein (aP2) and Lipoprotein lipase (Lpl). Next, adenovirus overexpression of LXRα does not affect intramuscular adipocytes adipogenesis manifested by Oil Red O signal measurement and adipogenic specific genes detection. Mechanically, we found that both CCAAT enhancer binding protein beta (Cebpβ) and Kruppel like factor 8 (Klf8) are potential targets of LXRα, indicated by having putative binding sites of LXRα at the promoter of these genes and similar expression pattern during adipogenesis comparing to LXRα. Importantly, mRNA levels of Cebpβ and Klf8 are downregulated significantly in goat LXRα knockdown intramuscular adipocyte. These results demonstrate that loss function of LXRα inhibits intramuscular adipogenesis possibly through down-regulation of Cebpβ and Klf8. Our research will provide new insights into mechanical regulation of goat IMF deposition. MDPI 2018-10-05 /pmc/articles/PMC6213902/ /pubmed/30301149 http://dx.doi.org/10.3390/ijms19103037 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Xiong, Yan
Xu, Qing
Lin, Sen
Wang, Yong
Lin, Yaqiu
Zhu, Jiangjiang
Knockdown of LXRα Inhibits Goat Intramuscular Preadipocyte Differentiation
title Knockdown of LXRα Inhibits Goat Intramuscular Preadipocyte Differentiation
title_full Knockdown of LXRα Inhibits Goat Intramuscular Preadipocyte Differentiation
title_fullStr Knockdown of LXRα Inhibits Goat Intramuscular Preadipocyte Differentiation
title_full_unstemmed Knockdown of LXRα Inhibits Goat Intramuscular Preadipocyte Differentiation
title_short Knockdown of LXRα Inhibits Goat Intramuscular Preadipocyte Differentiation
title_sort knockdown of lxrα inhibits goat intramuscular preadipocyte differentiation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6213902/
https://www.ncbi.nlm.nih.gov/pubmed/30301149
http://dx.doi.org/10.3390/ijms19103037
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