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This study provides the first evidence of functional compensation whereby increased expression of CES3 restores intracellular cholesteryl ester hydrolytic activity and free cholesterol efflux in CES1 (zeige CES1 Antikörper)-deficient cells.
Studies indicate that CES3 mRNA isoform expression in several tissues, particularly in colon, trachea and in brain.
CES3 seems to have a lower catalytic efficiency than the other two CESs for selected substrates.
pharmacogenomic characterization of human carboxylesterase 1A1 (zeige SLC45A2 Antikörper), 1A2, and 1A3 genes
Hepatic Ces3 modulates the hydrolysis of lipoprotein-delivered cholesterol esters and thereby regulates free cholesterol and bile acid secretion into the feces.
This gene encodes a member of the carboxylesterase large family. The family members are responsible for the hydrolysis or transesterification of various xenobiotics, such as cocaine and heroin, and endogenous substrates with ester, thioester, or amide bonds. They may participate in fatty acyl and cholesterol ester metabolism, and may play a role in the blood-brain barrier system. This gene is expressed in several tissues, particularly in colon, trachea and in brain, and the protein participates in colon and neural drug metabolism. Multiple alternatively spliced transcript variants encoding distinct isoforms have been reported, but the biological validity and/or full-length nature of some variants have not been determined.
, carboxylesterase 3 (brain)
, esterase 31
, liver carboxylesterase 31 homolog
, FAEE synthase
, carboxyesterase ES-10
, carboxylesterase 3
, fatty acid ethyl ester synthase
, liver carboxylesterase 10
, pI 6.1 esterase
, Es-male carboxylesterase
, liver carboxylesterase 31