Adipose triglyceride lipase
Lua error in Module:Infobox_gene at line 53: attempt to index field 'wikibase' (a nil value). Adipose triglyceride lipase, also known as patatin-like phospholipase domain-containing protein 2 and ATGL, is an enzyme that in humans is encoded by the PNPLA2 gene.[1][2][3] ATGL catalyses the first reaction of lipolysis,[4] where triacylglycerols are hydrolysed to diacylglycerols.[5]
Properties
[edit | edit source]ATGL has very high substrate specificity for triacylglycerols.[6] It contains a catalytic dyad using serine-aspartic acid.[5]
Function
[edit | edit source]ATGL catalyses the first reaction of lipolysis.[4] It hydrolysis triacylglycerols to diacylglycerols[5] by attacking the fatty acid attached to carbon-3 of glycerol.
ATGL acts as a control mechanism of lipolysis, as variations in diacylglycerol concentration impact enzymes in later stages of lipolysis.[7]
Clinical significance
[edit | edit source]Defects in ATGL can cause problems in lipolysis, leading to neutral lipid storage disease.[8] As triacylglycerols are not hydrolysed to diacylglycerols, there is a build-up of triacylglycerol droplets in granulocytes.[8]
ATGL is regulated by insulin, and is similar to structure with adiponutrin, a protein that is regulated by nutrition. When there is a lack of insulin, there is an increased expression of the ATGL protein. Because adipose tissue triglyceride is a major form of energy storage, the study of how ATGL regulation and dysregulation can lead to potential problems will increase understanding of the pathophysiology behind metabolic disorders.[9] ATGL is also the key enzyme that would be able to maintain a balance between mobilization and lipid storage. Lipolytic breakdown performed by ATGL would impact regulatory functions including but not limited to cell death, growth, signaling, metabolism, and gene expression.[10][11]
Regulation
[edit | edit source]There must be mechanisms set to maintain the balance between energy storage, and energy release; a dysregulation in the equilibrium result in metabolic disorder, a prime one being diabetes.[9] Adipose Triglyceride Lipase (ATGL) can undergo activation through two different pathways: transcriptionally and through post-translational modification. Through the transcriptional pathway, Beta-adrenergic, a receptor that can form a complex with agonist such as epinephrine, results in the signal transduction pathway activation of Adipose Triglyceride Lipase (ATGL). The alternative pathway is through a post-translational modification specifically phosphorylation of a serine 406 residue located on the enzyme by a kinase known as AMP activated protein kinase (AMPK). Both pathways facilitate the activation of the enzyme, resulting in the breakdown of triglyceride.[12]
Insulin is a hormone that regulates the enzyme ATGL, it inhibits the enzyme, favoring lipid storage over lipolysis.[9] One pathway of inhibition of ATGL when insulin is present is the activation of SIRT1, which inhibits FoxO1.[12][13] Specifically, FoxO1 is repressed from localizing to the nucleus by deacetylation in adipocytes.[12][14]
References
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Further reading
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External links
[edit | edit source]- Human PNPLA2 genome location and PNPLA2 gene details page in the UCSC Genome Browser.