Mice lacking lipid droplet-associated hydrolase, a gene linked to human prostate cancer, have normal cholesterol ester metabolism

Autor(en): Kory, Nora
Grond, Susanne
Kamat, Siddhesh S.
Li, Zhihuan
Krahmer, Natalie
Chitraju, Chandramohan
Zhou, Ping
Frohlich, Florian 
Semova, Ivana
Ejsing, Christer
Zechner, Rudolf
Cravatt, Benjamin F.
Farese, Jr., Robert V.
Walther, Tobias C.
Stichwörter: ACCUMULATION; ACTIVATION; animal models; Biochemistry & Molecular Biology; BREAST; cholesterol efflux; ENZYMES; EXPRESSION; HORMONE-SENSITIVE LIPASE; lipase; lipoprotein metabolism; LOCI; PROTEINS; RISK VARIANTS; triglycerides
Erscheinungsdatum: 2017
Herausgeber: AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
Journal: JOURNAL OF LIPID RESEARCH
Volumen: 58
Ausgabe: 1
Startseite: 226
Seitenende: 235
Zusammenfassung: 
Variations in the gene LDAH (C2ORF43), which encodes lipid droplet-associated hydrolase (LDAH), are among few loci associated with human prostate cancer. Homologs of LDAH have been identified as proteins of lipid droplets (LDs). LDs are cellular organelles that store neutral lipids, such as triacylglycerols and sterol esters, as precursors for membrane components and as reservoirs of metabolic energy. LDAH is reported to hydrolyze cholesterol esters and to be important in macrophage cholesterol ester metabolism. Here, we confirm that LDAH is localized to LDs in several model systems. We generated a murine model in which Ldah is disrupted but found no evidence for a major function of LDAH in cholesterol ester or triacylglycerol metabolism in vivo, nor a role in energy or glucose metabolism.(Jlr) Our data suggest that LDAH is not a major cholesterol ester hydrolase, and an alternative metabolic function may be responsible for its possible effect on development of prostate cancer.
ISSN: 00222275
DOI: 10.1194/jlr.M072538

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