H.N. Ginsberg, W.V. Brown. Arterioscler Thromb Vasc Biol 2011;31:

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H.N. Ginsberg, W.V. Brown. Arterioscler Thromb Vasc Biol 2011;31:471-473

Under normal conditions, apoCIII gene expression and synthesis are regulated by several factors, including PPAR, PPARγ, Rev-erbα, farnesoid X receptor, insulin, glucose Under normal conditions, apoCIII gene expression and synthesis are regulated by several factors, including PPAR, PPARγ, Rev-erbα, farnesoid X receptor, insulin, glucose All are inhibitory except for glucose, which stimulates apoCIII expression. Plasma free fatty acids (FFA) stimulate apoCIII secretion, but it is not known whether this occurs at the transcriptional or posttranslational level. ApoCIII in plasma inhibits lipoprotein lipase–mediated catabolism of VLDL (and chylomicrons) and inhibits the uptake of VLDL (and chylomicron) remnants by the liver. In addition, apoCIII may increase VLDL assembly and secretion. B, In states of insulin resistance, any inhibitory role of insulin on apoCIII expression may be lost, whereas higher glucose levels, particularly in patients with type 2 diabetes mellitus, would further stimulate apoCIII expression. Increased plasma FFA delivery to the liver would exacerbate this problem. The results of dysregulated apoCIII synthesis and secretion would be defective lipoprotein lipase–mediated lipolysis of triglyceride-rich lipoproteins and reduced remnant lipoprotein clearance. Thus, dysregulated apoCIII synthesis and secretion could play a major role in the genesis of the diabetic, insulin-resistant dyslipidemia. In addition, accumulation of apo-CIII rich apoB-containing lipoproteins might have direct atherogenic consequences. H.N. Ginsberg, W.V. Brown. Arterioscler Thromb Vasc Biol 2011;31:471-473