Lipoprotein metabolism – Very-low-density lipoproteins (VLDLs) are synthesized predominantly in which organ?
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ABlood (circulating plasma)
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BLiver (hepatocytes)
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CIntestine (enterocytes)
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DPancreas (acinar cells)
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EAdipose tissue (adipocytes)
Answer
Correct Answer: Liver (hepatocytes)
Explanation
Introduction / Context:Lipoproteins transport lipids through the aqueous bloodstream. Each class has a distinct site of assembly and apolipoprotein composition. VLDLs carry endogenously synthesized triacylglycerols from the liver to peripheral tissues. Identifying their origin is core to dyslipidemia and cardiovascular biochemistry.
Given Data / Assumptions:
- VLDLs contain ApoB-100, ApoE, and ApoCs.
- Chylomicrons are of intestinal origin and carry dietary lipids.
- The liver exports endogenous triacylglycerols and cholesterol via VLDL.
Concept / Approach:Hepatocytes assemble VLDL particles in the endoplasmic reticulum, requiring microsomal triglyceride transfer protein for ApoB-100 lipidation. Secreted VLDL matures in plasma by acquiring ApoC-II and ApoE from HDL and is progressively lipolyzed by lipoprotein lipase, yielding IDL and LDL.
Step-by-Step Solution:
Differentiate exogenous (chylomicron) vs endogenous (VLDL) pathways.Identify ApoB isoform: ApoB-100 indicates hepatic origin.Conclude that VLDL is synthesized in the liver.Verification / Alternative check:Clinical markers link hepatic overproduction of VLDL with hypertriglyceridemia; genetic defects in MTP impair VLDL secretion, causing abetalipoproteinemia.
Why Other Options Are Wrong:
- Intestine produces chylomicrons (ApoB-48), not VLDL.
- Blood is a transport medium, not a site of synthesis.
- Pancreas/adipose do not assemble VLDL particles.
Common Pitfalls:Confusing chylomicron and VLDL origins because both carry triacylglycerols.
Final Answer:Liver (hepatocytes)