Mammalian Triacylglycerol Metabolism: Synthesis, Lipolysis, and Signaling

被引:272
作者
Coleman, Rosalind A. [1 ]
Mashek, Douglas G. [2 ]
机构
[1] Univ N Carolina, Dept Nutr, Chapel Hill, NC 27599 USA
[2] Univ Minnesota, Dept Food Sci & Nutr, St Paul, MN 55108 USA
关键词
HORMONE-SENSITIVE LIPASE; ADIPOSE TRIGLYCERIDE LIPASE; LYSOPHOSPHATIDIC ACID ACYLTRANSFERASE; LIPID STORAGE DISEASE; ACTIVATED PROTEIN-KINASE; MITOCHONDRIAL GLYCEROL-3-PHOSPHATE ACYLTRANSFERASE-1; SN-GLYCEROL; 3-PHOSPHATE; FREE FATTY-ACIDS; INSULIN-STIMULATED PHOSPHORYLATION; COA-DIACYLGLYCEROL ACYLTRANSFERASE;
D O I
10.1021/cr100404w
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
An overview of TAG metabolism as a dynamic process that allows its lipid participants to play numerous inter-related roles within cells is presented. For most synthetic pathways each step is catalyzed by a single enzyme unless specific regulation is required. Yet, in the glycerol-3-phosphate pathway of TAG synthesis, investigators have confirmed four independent GPAT isoforms, three AGPAT isoforms, three PAP isoforms, and two DGAT isoforms. The non-backcrossed mice resist weight gain on a high-fat diet. Their subdermal fat depots are absent, and their gonadal and brown adipose fat pads and adipocytes are smaller. The differences in fat pad size are not solely due to absent GPAT4 activity within the tissue, because although NEM-sensitive GPAT activity in brown adipose is 50% lower than in wild-type brown adipose, gonadal NEM-sensitive GPAT activity is identical.
引用
收藏
页码:6359 / 6386
页数:28
相关论文
共 436 条
[1]
Evidence for triacylglycerol synthesis in the lumen of microsomes via a lipolysis-esterification pathway involving carnitine acyltransferases [J].
Abo-Hashema, KAH ;
Cake, MH ;
Power, GW ;
Clarke, D .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (50) :35577-35582
[2]
AGPAT2 is mutated in congenital generalized lipodystrophy linked to chromosome 9q34 [J].
Agarwal, AK ;
Arioglu, E ;
de Almeida, S ;
Akkoc, N ;
Taylor, SI ;
Bowcock, AM ;
Barnes, RI ;
Garg, A .
NATURE GENETICS, 2002, 31 (01) :21-23
[3]
Functional characterization of human 1-acylglycerol-3-phosphate-O-acyltransferase isoform 9:: cloning, tissue distribution, gene structure, and enzymatic activity [J].
Agarwal, Anil K. ;
Sukumaran, Suja ;
Bartz, Rene ;
Barnes, Robert I. ;
Garg, Abhimanyu .
JOURNAL OF ENDOCRINOLOGY, 2007, 193 (03) :445-457
[4]
Functional characterization of human 1-acylglycerol-3-phosphate acyltransferase isoform 8: Cloning, tissue distributions gene structure, and enzymatic activity [J].
Agarwal, Anil K. ;
Barnes, Robert I. ;
Garg, Abhimanyu .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2006, 449 (1-2) :64-76
[5]
Enzymatic activity of the human 1-acylglycerol-3-phosphate-O-acyltransferase isoform 11: upregulated in breast and cervical cancers [J].
Agarwal, Anil K. ;
Garg, Abhimanyu .
JOURNAL OF LIPID RESEARCH, 2010, 51 (08) :2143-2152
[6]
Adipose Overexpression of Desnutrin Promotes Fatty Acid Use and Attenuates Diet-Induced Obesity [J].
Ahmadian, Maryam ;
Duncan, Robin E. ;
Varady, Krista A. ;
Frasson, Danubia ;
Hellerstein, Marc K. ;
Birkenfeld, Andreas L. ;
Samuel, Varman T. ;
Shulman, Gerald I. ;
Wang, Yuhui ;
Kang, Chulho ;
Sul, Hei Sook .
DIABETES, 2009, 58 (04) :855-866
[7]
Truncation of CGI-58 protein causes malformation of lamellar granules resulting in ichthyosis in Dorfman-Chanarin syndrome [J].
Akiyama, M ;
Sawamura, D ;
Nomura, Y ;
Sugawara, M ;
Shimizu, H .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2003, 121 (05) :1029-1034
[8]
Novel duplication mutation in the patatin domain of adipose triglyceride lipase (PNPLA2) in neutral lipid storage disease with severe myopathy [J].
Akiyama, Masashi ;
Sakai, Kaori ;
Ogawa, Masaya ;
McMillan, James R. ;
Sawamura, Daisuke ;
Shimizu, Hiroshi .
MUSCLE & NERVE, 2007, 36 (06) :856-859
[9]
Neutral lipid storage disease with subclinical myopathy due to a retrotransposal insertion in the PNPLA2 gene [J].
Akman, Hasan O. ;
Davidzon, Guido ;
Tanji, Kurenai ;
MacDermott, Emma J. ;
Larsen, Louann ;
Davidson, Mercy M. ;
Haller, Ronald G. ;
Szczepaniak, Lidia S. ;
Lehman, Thomas J. A. ;
Hirano, Michio ;
DiMauro, Salvatore .
NEUROMUSCULAR DISORDERS, 2010, 20 (06) :397-402
[10]
A splice site mutation confirms the role of LPIN2 in Majeed syndrome [J].
Al-Mosawi, Zakiya S. ;
Al-Saad, Khulood K. ;
Ijadi-Maghsoodi, Roya ;
El-Shanti, Hatem I. ;
Ferguson, Polly J. .
ARTHRITIS AND RHEUMATISM, 2007, 56 (03) :960-964