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Lipin 1 represses NFATc4 transcriptional activity in adipocytes to inhibit secretion of inflammatory factors.
- Source :
-
Molecular and cellular biology [Mol Cell Biol] 2010 Jun; Vol. 30 (12), pp. 3126-39. Date of Electronic Publication: 2010 Apr 12. - Publication Year :
- 2010
-
Abstract
- Lipin 1 is a bifunctional protein that regulates gene transcription and, as a Mg(2+)-dependent phosphatidic acid phosphatase (PAP), is a key enzyme in the biosynthesis of phospholipids and triacylglycerol. We describe here the functional interaction between lipin 1 and the nuclear factor of activated T cells c4 (NFATc4). Lipin 1 represses NFATc4 transcriptional activity through protein-protein interaction, and lipin 1 is present at the promoters of NFATc4 transcriptional targets in vivo. Catalytically active and inactive lipin 1 can suppress NFATc4 transcriptional activity, and this suppression may involve recruitment of histone deacetylases to target promoters. In fat pads from mice deficient for lipin 1 (fld mice) and in 3T3-L1 adipocytes depleted of lipin 1 there is increased expression of several NFAT target genes including tumor necrosis factor alpha, resistin, FABP4, and PPARgamma. Finally, both lipin 1 protein and total PAP activity are decreased with increasing adiposity in the visceral, but not subcutaneous, fat pads of ob/ob mice. These observations place lipin 1 as a potentially important link between triacylglycerol synthesis and adipose tissue inflammation.
- Subjects :
- 3T3-L1 Cells
Adipocytes drug effects
Aging metabolism
Animals
Calcium Signaling drug effects
DNA metabolism
Gene Expression Regulation drug effects
Histone Deacetylases metabolism
Hydroxamic Acids pharmacology
Mice
Nuclear Proteins deficiency
Nuclear Proteins genetics
Obesity genetics
PPAR alpha metabolism
Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha
Phosphatidate Phosphatase
Promoter Regions, Genetic genetics
Protein Binding drug effects
RNA, Messenger genetics
RNA, Messenger metabolism
Trans-Activators metabolism
Transcription Factors
Tumor Necrosis Factor-alpha genetics
Tumor Necrosis Factor-alpha metabolism
Adipocytes metabolism
Inflammation Mediators metabolism
NFATC Transcription Factors genetics
Nuclear Proteins metabolism
Repressor Proteins metabolism
Transcription, Genetic drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 1098-5549
- Volume :
- 30
- Issue :
- 12
- Database :
- MEDLINE
- Journal :
- Molecular and cellular biology
- Publication Type :
- Academic Journal
- Accession number :
- 20385772
- Full Text :
- https://doi.org/10.1128/MCB.01671-09