The ANGPTL3-4-8 model, a molecular mechanism for triglyceride trafficking

R Zhang - Open biology, 2016 - royalsocietypublishing.org
Open biology, 2016royalsocietypublishing.org
Lipoprotein lipase (LPL) is a rate-limiting enzyme for hydrolysing circulating triglycerides
(TG) into free fatty acids that are taken up by peripheral tissues. Postprandial LPL activity
rises in white adipose tissue (WAT), but declines in the heart and skeletal muscle, thereby
directing circulating TG to WAT for storage; the reverse is true during fasting. However, the
mechanism for the tissue-specific regulation of LPL activity during the fed–fast cycle has
been elusive. Recent identification of lipasin/angiopoietin-like 8 (Angptl8), a feeding …
Lipoprotein lipase (LPL) is a rate-limiting enzyme for hydrolysing circulating triglycerides (TG) into free fatty acids that are taken up by peripheral tissues. Postprandial LPL activity rises in white adipose tissue (WAT), but declines in the heart and skeletal muscle, thereby directing circulating TG to WAT for storage; the reverse is true during fasting. However, the mechanism for the tissue-specific regulation of LPL activity during the fed–fast cycle has been elusive. Recent identification of lipasin/angiopoietin-like 8 (Angptl8), a feeding-induced hepatokine, together with Angptl3 and Angptl4, provides intriguing, yet puzzling, insights, because all the three Angptl members are LPL inhibitors, and the deficiency (overexpression) of any one causes hypotriglyceridaemia (hypertriglyceridaemia). Then, why does nature need all of the three? Our recent data that Angptl8 negatively regulates LPL activity specifically in cardiac and skeletal muscles suggest an Angptl3-4-8 model: feeding induces Angptl8, activating the Angptl8–Angptl3 pathway, which inhibits LPL in cardiac and skeletal muscles, thereby making circulating TG available for uptake by WAT, in which LPL activity is elevated owing to diminished Angptl4; the reverse is true during fasting, which suppresses Angptl8 but induces Angptl4, thereby directing TG to muscles. The model suggests a general framework for how TG trafficking is regulated.
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