CES3 hydrolyses CHEST to CHOL and LCFA(-)

Stable Identifier
R-HSA-8937442
Type
Reaction [transition]
Species
Homo sapiens
Compartment
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In macrophage foam cells, the hydrolysis of cholesteryl esters (CHESTs) is the rate-limiting step in the removal of free cholesterol (CHOL) from these cells. CHOL is transported via transport vesicles and can be used for cellular functions or removed from the cell by ABCA1 to create new HDL particles. Accumulation of CHESTs in macrophage foam cells is key to atherosclerotic plaque formation and occurs as a result of an imbalance between CHOL influx and efflux pathways. The main hydrolase that hydrolyses CE in macrophages is neutral cholesterol ester hydrolase 1 (NCEH1). Carboxylesterases (CESs), usually involved in the hydrolysis of drugs, can also hydrolyse CHESTs with CES1 responsible for >70% of the total CES hydrolytic activity in macrophages, thus playing an important antiatherogenic role. CES1 knockdown studies reveal a compensatory increase in the expression of CES3, expressed at <30% of the level of CES1 in human macrophages, which restores intracellular CHEST hydrolytic activity and CHOL efflux (Zhao et al. 2012). Human CES3 isoproteins are predicted to be either secreted or retained in the cytosol (Holmes et al. 2010) but the exact location is currently unknown.

Literature References
PubMed ID Title Journal Year
22700792 Identification of a novel intracellular cholesteryl ester hydrolase (carboxylesterase 3) in human macrophages: compensatory increase in its expression after carboxylesterase 1 silencing

Zhao, B, Bie, J, Wang, J, Marqueen, SA, Ghosh, S

Am. J. Physiol., Cell Physiol. 2012
20422440 Mammalian carboxylesterase 3: comparative genomics and proteomics

Holmes, RS, Cox, LA, VandeBerg, JL

Genetica 2010
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Catalyst Activity
Title
carboxylic ester hydrolase activity of CES3 [cytosol]
Physical Entity
Activity
Orthologous Events
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Created