Expression of carboxylesterase and lipase genes in rat liver cell-types

• Published in: Biochemical and biophysical research communications 2008-09, Vol.374 (3), p.460-464
• Main Authors: Mello, Tommaso, Nakatsuka, Alice, Fears, Sharry, Davis, Wilhelmina, Tsukamoto, Hidekazu, Bosron, William F., Sanghani, Sonal P.
• Format: Article
• Language: English
• Subjects: Adipocytes triglyceride lipase; Animals; Carboxylesterases; Carboxylic Ester Hydrolases - genetics; Cell Separation; Cells, Cultured; Endothelial Cells - enzymology; Gene Expression; Hepatic stellate cells; Hepatocytes - enzymology; Kupffer Cells - enzymology; Lipase - genetics; Lipoprotein lipase; Lipoprotein Lipase - genetics; Liver - cytology; Liver - enzymology; Polymerase Chain Reaction; Rats; Real-time PCR; Retinyl palmitate; Vitamin A; Vitamin A - metabolism
• ISSN: 0006-291X; 1090-2104
• DOI: 10.1016/j.bbrc.2008.07.024

Approximately 80% of the body vitamin A is stored in liver stellate cells with in the lipid droplets as retinyl esters. In low vitamin A status or after liver injury, stellate cells are depleted of the stored retinyl esters by their hydrolysis to retinol. However, the identity of retinyl ester hydrolase(s) expressed in stellate cells is unknown. The expression of carboxylesterase and lipase genes in purified liver cell-types was investigated by real-time PCR. We found that six carboxylesterase and hepatic lipase genes were expressed in hepatocytes. Adipose triglyceride lipase was expressed in Kupffer cells, stellate cells and endothelial cells. Lipoprotein lipase expression was detected in Kupffer cells and stellate cells. As a function of stellate cell activation, expression of adipose triglyceride lipase decreased by twofold and lipoprotein lipase increased by 32-fold suggesting that it may play a role in retinol ester hydrolysis during stellate cell activation.