Diacylglycerol acyltransferase 2 links glucose utilization to fatty acid oxidation in the brown adipocytes

Irshad, Z, Dimitri, F, Christian, M ORCID logoORCID: https://orcid.org/0000-0002-1616-4179 and Zammit, VA, 2017. Diacylglycerol acyltransferase 2 links glucose utilization to fatty acid oxidation in the brown adipocytes. Journal of Lipid Research, 58 (1), pp. 15-30. ISSN 0022-2275

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Abstract

Brown adipose tissue uptake of glucose and fatty acids is very high during nonshivering thermogenesis. Adrenergic stimulation markedly increases glucose uptake, de novo lipogenesis, and FA oxidation simultaneously. The mechanism that enables this concerted response has hitherto been unknown. Here, we find that in primary brown adipocytes and brown adipocyte-derived cell line (IMBAT-1), acute inhibition and longer-term knockdown of DGAT2 links the increased de novo synthesis of fatty acids from glucose to a pool of TAG that is simultaneously hydrolyzed, providing FA for mitochondrial oxidation. DGAT1 does not contribute to this pathway, but uses exogenous FA and glycerol to synthesize a functionally distinct pool of TAG to which DGAT2 also contributes. The DGAT2-dependent channelling of 14C from glucose into TAG and CO2 was reproduced in β3-agonist-stimulated primary brown adipocytes. Knockdown of DGAT2 in IMBAT-1 affected the mRNA levels of UCP1 and genes important in FA activation and esterification. Therefore, in β3-agonist activated brown adipocytes, DGAT2 specifically enables channelling of de novo synthesized FA into a rapidly mobilized pool of TAG, which is simultaneously hydrolyzed to provide substrates for mitochondrial fatty acid oxidation

Item Type: Journal article
Publication Title: Journal of Lipid Research
Creators: Irshad, Z., Dimitri, F., Christian, M. and Zammit, V.A.
Publisher: American Society for Biochemistry and Molecular Biology
Date: January 2017
Volume: 58
Number: 1
ISSN: 0022-2275
Identifiers:
Number
Type
10.1194/jlr.m068197
DOI
Rights: Copyright © 2017 by the American Society for Biochemistry and Molecular Biology, Inc.
Divisions: Schools > School of Science and Technology
Record created by: Linda Sullivan
Date Added: 09 Aug 2019 10:20
Last Modified: 09 Aug 2019 10:20
URI: https://irep.ntu.ac.uk/id/eprint/37206

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