Hepatic lipase

Hepatic lipase falls under a class of enzymes known as hydrolases. Its function is to hydrolyze triacylglycerol to diacylglycerol and carboxylate (free fatty acids) with the addition of water.[10] The substrate, triacylglycerol, comes from IDL (intermediate-density lipoprotein) and the release of free fatty acids converts IDL into LDL (low-density lipoprotein).[7] These remaining remnants of LDL can be sent back to the liver, where it can be stored for later use or broken down to harness its energy. It can also be sent to peripheral cells for its cholesterol and used in anabolic pathways to build molecules that the cell needs such as hormones that include a cholesterol backbone.[11]

To prevent the build-up of plaque (also referred to as a lipid pool), nascent HDL molecules which are low in triglycerides, take off free fatty acids from the plaques through the help of ABCL1 proteins. These proteins help transfer free fatty acids from plaques in the arteries to HDL.[8] This process creates HDL3 (High density lipoprotein 3), a mature HDL molecule that has been esterified by another enzyme known as LCAT.[11] More free fatty acids can be taken up from the plaque by SR-B1 receptors, which convert HDL3 to HDL2 which contains higher concentrations of free fatty acids.[7] HDL2 can then interact with LDL and IDL by transferring over fatty acids that have accumulated in the plaque. Hepatic lipase can then catalyze the conversion of IDL to LDL by breaking down triacylglycerides in IDL and release free fatty acids to be used by other cells with low concentrations of cholesterol or stored in the liver for later use.[8]

The function of hepatic lipase in regulating the formation and degradation of plaque (lipid pools) in the arteries of an organism. Note that ABCL1 protein, by transferring fatty acids from the plaque to HDL, creates HDL3. The same process is followed by SRB1, converting HDL3 to HDL2.

The human body contains two inactive forms of HL. One inactive form is found on the liver bound to HSPG (heparin sulfate proteoglycans) and the second inactive form is found in the blood bound to HDL, inactivated by the proteins on the surface of the lipoprotein. The activation of HL occurs in two steps. First, HDL that makes its way to the liver, binds to HL thereby removing the heparan sulfate proteoglycan and freeing up the hepatic lipase into the bloodstream, but HL is still inactive due to the proteins on the surface of the lipoprotein. Second, HDL unbinds from HL to activate HL enzymes in the blood.[6]

HDL has been found to be regulated by electrostatic interactions with lipoproteins such as HDL. When HDL takes up free fatty acids from cells to prevent plaque build-up, it begins to increase its overall negative charge and instead stimulates HL to catalysis the triacylglycerides inside of VLDL (very low density lipoprotein). This is because the build-up of negative charge in HDL inhibits binding, but will allow HL to catalyze other lipoproteins. Other lipoproteins, such as ApoE, works in a similar way by inhibiting binding of HL and HDL but will allow HL to catalyze other lipoproteins.[8]

Other factors that contribute the regulation of HL are due to sex differences between women and men. It has been shown that women contain lower levels of ApoE along with an increased amount of free HL enzymes in their circulatory system when compared to men. The production of estrogen in women is also believed to reduce the activity of HL by serving as an inhibitor of gene transcription.[7]

Secretion of HDL from the liver into the circulatory system regulates the release of HL into the body's bloodstream. This is because factors that increase the release of HDL (such as fasting, leading to low levels of HDL) increases the amount of HL bound to HDL and released into the bloodstream. Another lipoprotein, ApoA-I, which increases release of HDL was shown to have a similar effect by mutating the gene that coded it. Mutated ApoA-I protein caused a decrease in HL release and thus decreased the amount of HL bound to HDL and released into the bloodstream.[7]

Hepatic lipase deficiency is a rare, autosomal recessive disorder that results in elevated high-density lipoprotein (HDL) cholesterol due to a mutation in the hepatic lipase gene. Clinical features are not well understood and there are no characteristic xanthomas. There is an association with a delay in atherosclerosis in an animal model.[6]

In many studies that have been conducted, hepatic lipase is also closely related to obesity. In one test, an experiment was created by Cedó et al. where mouse cells were created to have a mutated HL protein that has lost its function. They found that a build-up of triglyceride levels led to nonalcoholic fatty liver disease. This was due to HL's inability to convert the triacylglycerides in IDL, and thereby creating LDL. Thus, the inability of endothelial cells to take up free fatty acids becomes higher and more IDL gets stored in the liver. This deficiency in HL also leads to liver inflammation and obesity problems. In the experiment though, mouse HL is found unbound to heparan sulfate proteoglycans (HSPG) whereas human HL is found attached to heparan sulfate proteoglycans (HSPG), deactivating HL until bound to IDL. More experiments must be performed to determine the potential effects in humans.[8]

• hepatic+lipase,+human at the U.S. National Library of Medicine Medical Subject Headings (MeSH)