Lipoprotein receptors in the liver. Control signals for plasma cholesterol traffic.
Open accessAbstract
A decade of intense investigation has established a central role for lipoprotein receptors in regulating plasma cholesterol traffic. These receptors bind cholesterol-carrying lipoproteins and transport them into cells by receptor-mediated endocytosis. The receptor for low density lipoprotein (LDL) was the first discovered; it has been purified and its structure characterized. The LDL receptor was described in cultured human fibroblasts; identical receptors are now known to function in liver as well as in extrahepatic tissues. Operationally, the LDL/LDL receptor system can be considered the primary transport mechanism for endogenous cholesterol. Dietary cholesterol, on the other hand, is transported from the intestine in chylomicron remnants, which enter hepatocytes via distinct chylomicron remnant receptors. The chylomicron remnant/remnant receptor system is to exogenous cholesterol transport as the LDL/LDL receptor system is to endogenous cholesterol transport. In this article, we review recent developments in this rapidly advancing field.
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LDL biology is mostly relevant for peripheral diseases.
“While LDL biology is mostly relevant for peripheral diseases32,54,55”
From Decreased lipidated ApoE‐receptor interactions confer protection against pathogenicity of ApoE and its lipid cargoes in lysosomes (2025) · cites this paper as [54]
The paper emphasizes hepatic LDL receptors rather than presenting LDL biology as mostly peripheral. In “Control Signals for Plasma Cholesterol Traffic” (pp. 1–2), it says that more than half of LDL receptors are in the liver and that changes in hepatic receptor activity alter plasma LDL levels. It also discusses extrahepatic tissues and atherosclerosis, but does not characterize LDL biology as mostly relevant to peripheral diseases. (LLM, conf=0.75)
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- Authors
- Brown, M. S., & Goldstein, J. L.
- ORCID
- Goldstein, J L
- Venue
- Journal of Clinical Investigation
- Published
- 1983-09-01
- Volume
- 72
- Issue
- 3
- Pages
- 743-747
- ISSN
- 0021-9738 (ISSN-L)
- PMC
- PMC1129238
- OpenAlex
- W2137716547
- Cited by
- 545
- References
- 48
- Citations by year
- 2026: 3 · 2025: 1 · 2024: 4 · 2023: 4 · 2022: 2 · 2021: 5 · 2020: 9 · 2019: 8 · 2018: 3 · 2017: 3 · 2016: 1 · 2015: 6 · 2014: 9 · 2013: 5 · 2012: 13
- FWCI
- 66.68
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Journal of Clinical Investigation (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (HL20948)
- Topics
- Health Sciences › Medicine › Surgery › Cholesterol and Lipid Metabolism
- Health Sciences › Medicine › Surgery › Lipoproteins and Cardiovascular Health
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Lipid metabolism and disorders
- Keywords
- lipoprotein receptors, liver, LDL receptor, receptor-mediated endocytosis, chylomicron remnants, dietary cholesterol, hepatocytes
- MeSH terms
- Animals, Apolipoproteins, Apolipoproteins E, Apoproteins, Binding, Competitive, Cholesterol, Cyclohexanones, Dogs, Guinea Pigs, Cricetinae, Humans, Hyperlipoproteinemia Type II, Liver, Macaca mulatta, Molecular Weight, Rabbits, Receptors, Cell Surface, Receptors, LDL, Receptors, Lipoprotein, Rats
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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