The adipsin-acylation stimulating protein system and regulation of intracellular triglyceride synthesis.

Article Details

Citation

Baldo A, Sniderman AD, St-Luce S, Avramoglu RK, Maslowska M, Hoang B, Monge JC, Bell A, Mulay S, Cianflone K

The adipsin-acylation stimulating protein system and regulation of intracellular triglyceride synthesis.

J Clin Invest. 1993 Sep;92(3):1543-7.

PubMed ID
8376604 [ View in PubMed
]
Abstract

We have previously characterized an activity from human plasma that markedly stimulates triglyceride synthesis in cultured human skin fibroblasts and human adipocytes. Based on its in vitro activity we named the active component acylation stimulating protein (ASP). The molecular identity of the active serum component has now been determined. NH2-terminal sequence analysis, ion spray ionization mass spectroscopy, and amino acid composition analysis all indicate that the active purified protein is a fragment of the third component of plasma complement, C3a-desArg. As well, reconstitution experiments with complement factors B, D, and complement C3, the components necessary to generate C3a, have confirmed the identity of ASP as C3a. ASP appears to be the final effector molecule generated by a novel regulatory system that modulates the rate of triglyceride synthesis in adipocytes.

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Complement C3P01024Details