How Triglycerdies are Broken Down in Your Circulation
One way your body can clear excess fat blobs out of your circulatory system - assuming you give it the chance to do so.
Study Title:GPIHBP1 Is Responsible for the Entry of Lipoprotein Lipase into Capillaries
The lipolytic processing of triglyceride-rich lipoproteins by lipoprotein lipase (LPL) is the central event in plasma lipid metabolism, providing lipids for storage in adipose tissue and fuel for vital organs such as the heart. LPL is synthesized and secreted by myocytes and adipocytes, but then finds its way into the lumen of capillaries, where it hydrolyzes lipoprotein triglycerides. The mechanism by which LPL reaches the lumen of capillaries has remained an unresolved problem of plasma lipid metabolism. Here, we show that GPIHBP1 is responsible for the transport of LPL into capillaries. In Gpihbp1-deficient mice, LPL is mislocalized to the interstitial spaces surrounding myocytes and adipocytes. Also, we show that GPIHBP1 is located at the basolateral surface of capillary endothelial cells and actively transports LPL across endothelial cells. Our experiments define the function of GPIHBP1 in triglyceride metabolism and provide a mechanism for the transport of LPL into capillaries.
From press release:
New findings reported in the July issue of Cell Metabolism, are offering new leads as to why some people might suffer from high levels of triglycerides. High triglycerides are a risk factor for atherosclerosis and cardiovascular disease. They can also lead to inflammation of the pancreas, the researchers said.
The team led by Loren Fong and Stephen Young of the University of California, Los Angeles, has identified the component responsible for bringing a key triglyceride-processing enzyme (called lipoprotein lipase or LPL for short) into the capillaries, where it does its work.
“LPL is required for normal metabolism of triglycerides in blood,” Fong said. “If there is no LPL, triglycerides accumulate.”
Scientists have known for decades that the LPL enzyme is produced in fat and muscle before it makes its way into blood vessels. What they didn’t know until now was how it got there.
It seems that a protein known as GPIHBP1 is the key. Mice lacking that protein end up with LPL built up outside of their muscle and fat tissue instead of where it belongs in capillaries. They show that GPIHBP1 normally sits on the surface of capillary cells, where it actively transports LPL.
The new findings offer an explanation for what had been a surprising finding; Gpihbp1-deficient mice develop severe hypertriglyceridemia, even when they eat a normal diet of mouse chow. Very recently, other researchers have also shown that some people with elevated triglyceride levels carry mutations in their GPIHBP1 gene.
Fong and Young say they don’t yet know exactly how GPIHBP1 does its job of transporting LPL into capillaries. It’s likely that other as-yet unknown players are involved. Their team also suspects that GPIHBP1 may influence triglyceride metabolism in other ways, aside from its transport function.
There is also much left to learn about how the process is regulated in response to diet or other factors. For instance, “if you eat a fatty meal with more lipids, does this transport go faster?” Fong asked.
The findings may help sort out the causes of hypertriglyceridemia, which in many instances remain unclear.
“In humans, mechanisms for severe cases of hypercholesterolemia have come into focus, but the same cannot be said for many cases of severe hypertriglyceridemia,” the researchers wrote. Many patients with very high triglyceride levels don’t have mutations in any of the genes with known links to the condition and some have no obvious abnormalities in LPL levels either.
“It seems possible that defective transport of LPL into the capillaries could underlie at least some cases of hypertriglyceridemia in humans,” they said.
1.Brandon S.J. Davies, Anne P. Beigneux, Richard H. Barnes, Yiping Tu, Peter Gin, Michael M. Weinstein, Chika Nobumori, Rakel Nyrén, Ira Goldberg, Gunilla Olivecrona, André Bensadoun, Stephen G. Young, Loren G. Fong. GPIHBP1 Is Responsible for the Entry of Lipoprotein Lipase into Capillaries Cell Metabolism 2010 July
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