出版社：American Society for Biochemistry and Molecular Biology
摘要：Acylation stimulating protein (ASP) is a 76 amino acid fragment of the third component of complement (C3) which is generated by the interaction of adipsin and factor B with C3. In vitro studies have shown that ASP can markedly increase triglyceride synthesis in adipocytes. To test the ASP pathway in vivo, C3-deficient mice, and therefore ASP-deficient mice, were generated and oral fat loads were conducted in wild-type (C3+/+) and mutant (C3–/–) animals. The principal results were: 1 ) postprandial triglyceride clearance was significantly delayed in mutant compared to wild-type mice; 2 ) this difference was more pronounced in males compared to females; 3 ) in both males and females, the differences were more pronounced in the second half of the postprandial period; 4 ) fasting and postprandial free fatty acid (FFA) were higher in C3(–/–) than in C3(+/+) males; and 5 ) intraperitoneal administration of ASP accelerated triglyceride clearance in C3(–/–) males. The data are consistent therefore, with the hypothesis that the ASP pathway is an important physiologic determinant of normal postprandial triglyceride clearance. —Murray, I., A. D. Sniderman, and K. Cianflone. Mice lacking acylation stimulating protein (ASP) have delayed postprandial triglyceride clearance. J. Lipid Res. 1999. 40: 1671–1676.
