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The Role of Proton-Coupled Amino Acid Transporter 2 (SLC36A2) in Cold-Induced Thermogenesis of Mice

Brown adipocytes mainly utilize glucose and fatty acids to produce energy, which play key roles in thermogenesis. Furthermore, brown adipocytes also utilize other substrates, such as amino acids, for energy expenditure in various conditions. Here, we report the new physiological roles of proton-coup...

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Autores principales: Shu, Hui, Zhang, Jie, Cheng, Dawei, Zhao, Xiaorui, Ma, Yue, Zhang, Chi, Zhang, Yong, Jia, Zhihao, Liu, Zhiwei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10458080/
https://www.ncbi.nlm.nih.gov/pubmed/37630739
http://dx.doi.org/10.3390/nu15163552
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author Shu, Hui
Zhang, Jie
Cheng, Dawei
Zhao, Xiaorui
Ma, Yue
Zhang, Chi
Zhang, Yong
Jia, Zhihao
Liu, Zhiwei
author_facet Shu, Hui
Zhang, Jie
Cheng, Dawei
Zhao, Xiaorui
Ma, Yue
Zhang, Chi
Zhang, Yong
Jia, Zhihao
Liu, Zhiwei
author_sort Shu, Hui
collection PubMed
description Brown adipocytes mainly utilize glucose and fatty acids to produce energy, which play key roles in thermogenesis. Furthermore, brown adipocytes also utilize other substrates, such as amino acids, for energy expenditure in various conditions. Here, we report the new physiological roles of proton-coupled amino acid transporters, SLC36A2 and SLC36A3, on global energy metabolism. The relative mRNA expression levels of both Slc36a2 and Slc36a3 were all highest in brown adipose tissue. We then generated global Slc36a2 and Slc36a3 knockout mice to investigate their functions in metabolism. Neither loss of Slc36a2 nor Slc36a3 affected the body weight and body composition of the mice. Slc36a2 knockout mice exhibited increased oxygen consumption during the daytime. After cold treatment, inhibition of Slc36a2 significantly decreased the mass of brown adipose tissue compared to wildtype mice, while it lowered the expression level of Cpt1a. Moreover, the serum lipid levels and liver mass were also decreased in Slc36a2 knockout mice after cold treatment. On the contrary, Slc36a3 knockout impaired glucose tolerance and up-regulated serum LDL-cholesterol concentration. Thus, SLC36A2 and SLC36A3 play central and different roles in the energy metabolism of the mice.
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spelling pubmed-104580802023-08-27 The Role of Proton-Coupled Amino Acid Transporter 2 (SLC36A2) in Cold-Induced Thermogenesis of Mice Shu, Hui Zhang, Jie Cheng, Dawei Zhao, Xiaorui Ma, Yue Zhang, Chi Zhang, Yong Jia, Zhihao Liu, Zhiwei Nutrients Article Brown adipocytes mainly utilize glucose and fatty acids to produce energy, which play key roles in thermogenesis. Furthermore, brown adipocytes also utilize other substrates, such as amino acids, for energy expenditure in various conditions. Here, we report the new physiological roles of proton-coupled amino acid transporters, SLC36A2 and SLC36A3, on global energy metabolism. The relative mRNA expression levels of both Slc36a2 and Slc36a3 were all highest in brown adipose tissue. We then generated global Slc36a2 and Slc36a3 knockout mice to investigate their functions in metabolism. Neither loss of Slc36a2 nor Slc36a3 affected the body weight and body composition of the mice. Slc36a2 knockout mice exhibited increased oxygen consumption during the daytime. After cold treatment, inhibition of Slc36a2 significantly decreased the mass of brown adipose tissue compared to wildtype mice, while it lowered the expression level of Cpt1a. Moreover, the serum lipid levels and liver mass were also decreased in Slc36a2 knockout mice after cold treatment. On the contrary, Slc36a3 knockout impaired glucose tolerance and up-regulated serum LDL-cholesterol concentration. Thus, SLC36A2 and SLC36A3 play central and different roles in the energy metabolism of the mice. MDPI 2023-08-11 /pmc/articles/PMC10458080/ /pubmed/37630739 http://dx.doi.org/10.3390/nu15163552 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Shu, Hui
Zhang, Jie
Cheng, Dawei
Zhao, Xiaorui
Ma, Yue
Zhang, Chi
Zhang, Yong
Jia, Zhihao
Liu, Zhiwei
The Role of Proton-Coupled Amino Acid Transporter 2 (SLC36A2) in Cold-Induced Thermogenesis of Mice
title The Role of Proton-Coupled Amino Acid Transporter 2 (SLC36A2) in Cold-Induced Thermogenesis of Mice
title_full The Role of Proton-Coupled Amino Acid Transporter 2 (SLC36A2) in Cold-Induced Thermogenesis of Mice
title_fullStr The Role of Proton-Coupled Amino Acid Transporter 2 (SLC36A2) in Cold-Induced Thermogenesis of Mice
title_full_unstemmed The Role of Proton-Coupled Amino Acid Transporter 2 (SLC36A2) in Cold-Induced Thermogenesis of Mice
title_short The Role of Proton-Coupled Amino Acid Transporter 2 (SLC36A2) in Cold-Induced Thermogenesis of Mice
title_sort role of proton-coupled amino acid transporter 2 (slc36a2) in cold-induced thermogenesis of mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10458080/
https://www.ncbi.nlm.nih.gov/pubmed/37630739
http://dx.doi.org/10.3390/nu15163552
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