Abstract

Endothelial lipase (EL) is synthetized by endothelial cells and its main substrates are lipoprotein phospholipids. Over expression of EL reduces high density lipoprotein (HDL) cholesterol and phospholipids, in vivo and in vitro. Inhibition of the enzyme achieves the opposite effects. The synthesis of the enzyme is regulated by interleukin 1 and tumor necrosis factor a. These inflammatory cytokines play a role in diabetes and vascular disease. An increase in vascular mechanical forces, that play a role in atherogenesis, also increase the synthesis of EL. There is expression of EL in endothelial cells, macrophages and muscle cells of atherosclerotic lesions of coronary arteries of humans. This evidence leads to the suspicion that EL plays a role in atherogenesis. There are also higher plasma levels of EL in subjects with type 2 diabetes, who are especially susceptible to the development of vascular lesions. Therefore the inhibition of EL could play an important role in HDL metabolism and could be a new therapeutic strategy for the prevention of atherosclerosis.

Highlights

  • lipasa endotelial (LE) es una enzima de 482 aminoácidos que se identificó inicialmente en cultivo de células endoteliales de cordón umbilical humano (HUVEC) y en líneas celulares de macrófagos humanos THP-1 expuestos a LDL oxidadas[2,3]

  • Paradis M, Badellino, K, Rader D, Deshaies Y, Couture P, Archer W, et al Endothelial lipase is associated with inflammation in humans

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Summary

The role of endothelial lipase in atherogenesis

Endothelial lipase (EL) is synthetized by endothelial cells and its main substrates are lipoprotein phospholipids. The synthesis of the enzyme is regulated by interleukin 1 and tumor necrosis factor These inflammatory cytokines play a role in diabetes and vascular disease. Otro estudio realizado en niños sanos en edad escolar, mostró que la presencia de distintos polimorfismos en el gen de LE se asocia a variaciones en los niveles plasmáticos de c-HDL, lo que sugiere que las alteraciones genéticas de esta enzima podrían ser una de las determinantes en las variaciones del c-HDL14. Estudios in vitro han demostrado que LE actuaría remodelando las partículas de HDL, transformándolas en estructuras más pequeñas por pérdida de fosfolípidos, sin que exista disociación de apo A-I16, lo que la diferencia de LH, que produce una disociación de la apoproteína teniendo esta

Lugar de síntesis
Findings
Factores que modulan la actividad de LE
Full Text
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