Lipoprotein lipase: Difference between revisions
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{{DISPLAYTITLE:Lipoprotein lipase}} | |||
== | == Lipoprotein Lipase == | ||
[[File:LPL_homodimer.jpg|thumb|right|300px|Structure of lipoprotein lipase homodimer.]] | |||
'''Lipoprotein lipase''' (LPL) is an enzyme crucial for the metabolism of [[lipids]] in the body. It is primarily responsible for the hydrolysis of [[triglycerides]] in [[chylomicrons]] and [[very low-density lipoproteins]] (VLDL) into [[free fatty acids]] and [[glycerol]]. These products are then available for uptake by tissues such as [[muscle]] and [[adipose tissue]]. | |||
== Structure == | |||
Lipoprotein lipase is a member of the [[lipase]] family of enzymes. It is a homodimer, meaning it consists of two identical subunits. Each subunit contains a catalytic domain and a lipid-binding domain. The enzyme is anchored to the [[endothelial cells]] of capillaries in tissues that utilize fatty acids. | |||
== | == Function == | ||
LPL plays a critical role in lipid metabolism by breaking down triglycerides in lipoproteins. This process is essential for the delivery of fatty acids to tissues, where they can be used for energy production or stored as fat. LPL activity is regulated by several factors, including [[insulin]], which enhances its activity, and [[apolipoprotein C-II]], which acts as a cofactor. | |||
== Regulation == | |||
The activity of lipoprotein lipase is tightly regulated by nutritional and hormonal signals. During the fed state, insulin levels rise, leading to increased LPL activity in adipose tissue, promoting fat storage. Conversely, during fasting, LPL activity in muscle tissue is upregulated to provide energy from fatty acids. | |||
== | == Clinical Significance == | ||
Deficiencies or mutations in the LPL gene can lead to disorders such as [[familial chylomicronemia syndrome]], characterized by elevated triglyceride levels and increased risk of [[pancreatitis]]. Understanding LPL function and regulation is important for developing treatments for [[hyperlipidemia]] and related cardiovascular diseases. | |||
== Related pages == | |||
* [[ | * [[Triglyceride]] | ||
* [[ | * [[Chylomicron]] | ||
* [[ | * [[Very low-density lipoprotein]] | ||
* [[ | * [[Apolipoprotein C-II]] | ||
* [[ | * [[Hyperlipidemia]] | ||
[[Category:Enzymes]] | [[Category:Enzymes]] | ||
[[Category:Lipid metabolism]] | [[Category:Lipid metabolism]] | ||
Latest revision as of 11:18, 15 February 2025
Lipoprotein Lipase[edit]
Lipoprotein lipase (LPL) is an enzyme crucial for the metabolism of lipids in the body. It is primarily responsible for the hydrolysis of triglycerides in chylomicrons and very low-density lipoproteins (VLDL) into free fatty acids and glycerol. These products are then available for uptake by tissues such as muscle and adipose tissue.
Structure[edit]
Lipoprotein lipase is a member of the lipase family of enzymes. It is a homodimer, meaning it consists of two identical subunits. Each subunit contains a catalytic domain and a lipid-binding domain. The enzyme is anchored to the endothelial cells of capillaries in tissues that utilize fatty acids.
Function[edit]
LPL plays a critical role in lipid metabolism by breaking down triglycerides in lipoproteins. This process is essential for the delivery of fatty acids to tissues, where they can be used for energy production or stored as fat. LPL activity is regulated by several factors, including insulin, which enhances its activity, and apolipoprotein C-II, which acts as a cofactor.
Regulation[edit]
The activity of lipoprotein lipase is tightly regulated by nutritional and hormonal signals. During the fed state, insulin levels rise, leading to increased LPL activity in adipose tissue, promoting fat storage. Conversely, during fasting, LPL activity in muscle tissue is upregulated to provide energy from fatty acids.
Clinical Significance[edit]
Deficiencies or mutations in the LPL gene can lead to disorders such as familial chylomicronemia syndrome, characterized by elevated triglyceride levels and increased risk of pancreatitis. Understanding LPL function and regulation is important for developing treatments for hyperlipidemia and related cardiovascular diseases.
