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[Biochemistry](https://durgical.com/en/biochemistry/) · Topic

# Lipoprotein metabolism

Lipoproteins carry fat in the blood: the exogenous pathway delivers dietary fat, the endogenous pathway liver fat, and HDL returns cholesterol to the liver.

Updated 2026-11-01

## Key facts

- Exogenous: the gut builds chylomicrons (ApoB-48); LPL removes their triglyceride and the liver takes up remnants via ApoE.
- Endogenous: the liver secretes VLDL (ApoB-100); LPL turns it into IDL and then LDL, which the LDL receptor clears.
- Reverse transport: HDL picks up tissue cholesterol via ABCA1, LCAT esterifies it, and it reaches the liver via SR-BI or, through CETP, in ApoB particles.
- Key apos: B-48 (chylomicron), B-100 (VLDL/LDL, binds the receptor), C-II (activates LPL), E (remnant uptake), A-I (HDL, activates LCAT).

## In detail

- In the enterocyte, MTP loads triglyceride, cholesterol and phospholipid onto ApoB-48: the chylomicron is born and leaves through the lymph (thoracic duct), bypassing the liver.
- In blood, HDL gives it ApoC-II and ApoE. In muscle and fat capillaries, LPL (activated by ApoC-II) releases the fatty acids.
- The shrunken chylomicron returns ApoC-II to HDL and becomes a cholesterol-rich remnant that the liver takes up via ApoE.
- The liver packs triglyceride made from surplus carbohydrate into VLDL with ApoB-100; LPL empties it, leaving IDL.
- Some IDL returns to the liver via ApoE; the rest loses more triglyceride to hepatic lipase and becomes cholesteryl-ester-rich LDL.
- LDL delivers cholesterol to tissues and liver via the LDL receptor; if it lingers in blood, it is oxidised in the artery wall and taken up by macrophages (foam cells).
- Nascent HDL (lipid-poor ApoA-I) takes cholesterol and phospholipid from cells via ABCA1; LCAT esterifies it and the particle becomes spherical.
- HDL hands cholesteryl ester to the liver via SR-BI, or CETP passes it to VLDL and LDL for triglyceride; the liver excretes it in bile.

## Clinical notes

- A lipid panel measures total cholesterol, HDL and triglycerides; LDL is usually calculated (Friedewald), unreliable when triglycerides are very high.
- Fredrickson classes: I (chylomicrons), IIa (LDL), IIb (LDL and VLDL), III (remnants), IV (VLDL), V (VLDL and chylomicrons).
- Statins, ezetimibe and PCSK9 inhibitors lower LDL; fibrates activate PPAR-α and raise LPL activity.

## Related conditions

- [Atherosclerosis and dyslipidaemia](https://durgical.com/en/conditions/atherosclerosis-and-dyslipidaemia/)
- [Familial hypercholesterolemia](https://durgical.com/en/conditions/familial-hypercholesterolemia/)
- [Familial chylomicronemia syndrome (lipoprotein lipase deficiency)](https://durgical.com/en/conditions/familial-chylomicronemia-syndrome/)
- [Abetalipoproteinemia (Bassen–Kornzweig syndrome)](https://durgical.com/en/conditions/abetalipoproteinemia/)
- [Familial dysbetalipoproteinemia (type III hyperlipoproteinemia)](https://durgical.com/en/conditions/familial-dysbetalipoproteinemia/)
- [Tangier disease](https://durgical.com/en/conditions/tangier-disease/)
- [Acute pancreatitis](https://durgical.com/en/conditions/acute-pancreatitis/)

## Related

- [Chylomicron](https://durgical.com/en/biochemistry/topics/chylomicron/)
- [VLDL (very-low-density lipoprotein)](https://durgical.com/en/biochemistry/topics/vldl/)
- [LDL (low-density lipoprotein)](https://durgical.com/en/biochemistry/topics/ldl/)
- [HDL (high-density lipoprotein)](https://durgical.com/en/biochemistry/topics/hdl/)
- [Lipoprotein lipase (LPL)](https://durgical.com/en/biochemistry/enzymes/lipoprotein-lipase/)
- [LCAT (lecithin–cholesterol acyltransferase)](https://durgical.com/en/biochemistry/enzymes/lcat/)
- [CETP (cholesteryl ester transfer protein)](https://durgical.com/en/biochemistry/enzymes/cetp/)
- [LDL receptor](https://durgical.com/en/biochemistry/enzymes/ldl-receptor/)
- [PCSK9](https://durgical.com/en/biochemistry/enzymes/pcsk9/)
- [Apolipoprotein B (ApoB-100 and ApoB-48)](https://durgical.com/en/biochemistry/enzymes/apolipoprotein-b/)
- [Apolipoprotein E (ApoE)](https://durgical.com/en/biochemistry/enzymes/apolipoprotein-e/)
- [Cholesterol](https://durgical.com/en/biochemistry/molecules/cholesterol/)
- [Bile acid synthesis](https://durgical.com/en/biochemistry/topics/bile-acid-synthesis/)
- [Cholesterol synthesis (mevalonate pathway)](https://durgical.com/en/biochemistry/pathways/cholesterol-synthesis/)

## Test yourself

Think of the answer, then tap the question to see it.

## Which apolipoprotein defines the chylomicron, and which LDL?

ApoB-48 on chylomicrons; ApoB-100 on VLDL, IDL and LDL.

## Why do chylomicrons reach the blood without passing through the liver?

They are too large for gut capillaries: they travel through lymphatics and the thoracic duct.

## Which steps make up reverse cholesterol transport?

Efflux through ABCA1 to ApoA-I, esterification by LCAT and delivery to the liver (SR-BI or via CETP), which sends it to bile.

## Which Fredrickson type is remnant accumulation?

Type III (dysbetalipoproteinaemia).

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Educational information, not medical advice. For any symptom, see a health professional.

Sources: [Plasma lipoprotein assembly, remodeling, and clearance (R-HSA-174824)](https://reactome.org/PathwayBrowser/#/R-HSA-174824) (Reactome, 2026); [Cholesterol | High Cholesterol | MedlinePlus](https://medlineplus.gov/cholesterol.html) (MedlinePlus, US National Library of Medicine, 2026); [Triglycerides | MedlinePlus](https://medlineplus.gov/triglycerides.html) (MedlinePlus, US National Library of Medicine, 2026); Textbook of Biochemistry for Medical Students, 6th ed. (Jaypee Brothers Medical Publishers (Vasudevan DM, Sreekumari S, Vaidyanathan K), 2011).

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