Copyright © 2016 Elsevier Inc. All rights reserved.

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Copyright © 2016 Elsevier Inc. All rights reserved. Chapter 26 Genetic Influences on Blood Lipids and Cardiovascular Disease Risk Copyright © 2016 Elsevier Inc. All rights reserved.

Copyright © 2016 Elsevier Inc. All rights reserved.

Copyright © 2016 Elsevier Inc. All rights reserved. FIGURE 26.1: The main lipids in lipoproteins are free and esterified cholesterol (C) and TG. The metabolism of TG, LDL cholesterol, and HDL cholesterol is shown. In TG metabolism, hydrolyzed dietary fats enter intestinal cells (enterocytes) via fatty acid (FA) transporters. Reconstituted TG is packaged with C ester and the apolipoprotein B (APOB) isoform B48 into chylomicrons (CMs) by microsomal TG-transfer protein (MTTP) through a vesicular pathway. CMs, secreted via the lymphatic system, enter the vena cava and circulate until they interact with LPL, the secretion of which depends on lipase-maturation factor 1 (not shown), and which is secured to endothelium by proteoglycans and glycosylphosphatidylinositol-anchored HDL-binding protein 1 (not shown). CMs contain apolipoproteins, including APOA5 (A5), APOC2 (C2), and APOC3 (C3). Released free FAs incompletely enter peripheral cells. In adipocytes, enzymes including acyl CoA:diacylglycerol acyltransferase (DGAT) resynthesize TG, which is hydrolyzed by adipose TG lipase (ATGL) and hormone sensitive lipase (HSL). CM remnants (CMRs) are taken up by hepatic LDL receptor (LDLR), in the absence of LDLR they are taken up by LDLR-related protein-1 (LRP1). In liver cells (hepatocytes), TG is packaged with cholesterol and the APOB isoform B100 into VLDL; the TG contained in VLDL is hydrolyzed by LPL, releasing FAs and VLDL remnants (IDL) that are hydrolyzed by hepatic lipase (HL), thereby yielding LDL. In LDL cholesterol metabolism, sterols in the intestinal lumen enter enterocytes via the Niemann-Pick C1-like 1 (NPC1L1) transporter and some are resecreted by heterodimeric ATP-binding cassette transporter G5/G8 (ABCG5/G8). In enterocytes, cholesterol is packaged with TG into CM. In hepatocytes, cholesterol is recycled or synthesized de novo, with 3-hydroxy-3-methylglutaryl coenzyme A reductase (HMGCR) being rate-limiting. LDL transports cholesterol from the liver to the periphery. LDL is endocytosed by peripheral cells and hepatocytes by LDLR, assisted by an adaptor protein (AP). Proprotein convertase subtilisin/kexin type 9 (PCSK9), when complexed to LDLR, short-circuits recycling of LDLR from the endosome, leading to its degradation (X). In HDL cholesterol metabolism, HDL, via APOA-I (A1), mediates reverse cholesterol transport by interacting with ATP-binding cassette A1 (ABCA1) and ABCG1 transporters on nonhepatic cells. LCAT esterifies cholesterol so it can be used in HDL cholesterol, which, after remodeling by CETP and by endothelial lipase (LIPG), enters hepatocytes via scavenger receptor class B type I (SRB1). Reprinted by permission from Macmillan Publishers Ltd. R.A. Hegele, Plasma lipoproteins: genetic influences and clinical implications, Nat. Rev. Genet. 10 (2009) 109121, copyright 2009. Copyright © 2016 Elsevier Inc. All rights reserved.