OLR1

Oxidized low-density lipoprotein receptor 1 (Ox-LDL receptor 1) also known as lectin-type oxidized LDL receptor 1 (LOX-1) is a protein that in humans is encoded by the OLR1 gene.[5][6]

OLR1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesOLR1, CLEC8A, LOX1, LOXIN, SCARE1, SLOX1, oxidized low density lipoprotein receptor 1
External IDsOMIM: 602601 MGI: 1261434 HomoloGene: 1910 GeneCards: OLR1
Gene location (Human)
Chr.Chromosome 12 (human)[1]
Band12p13.2Start10,158,301 bp[1]
End10,172,138 bp[1]
RNA expression pattern
More reference expression data
Orthologs
SpeciesHumanMouse
Entrez

4973

108078

Ensembl

ENSG00000173391

ENSMUSG00000030162

UniProt

P78380

Q9EQ09

RefSeq (mRNA)

NM_001172632
NM_001172633
NM_002543

NM_001301094
NM_001301096
NM_138648

RefSeq (protein)

NP_001166103
NP_001166104
NP_002534

NP_001288023
NP_001288025
NP_619589

Location (UCSC)Chr 12: 10.16 – 10.17 MbChr 6: 129.49 – 129.51 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

LOX-1 is the main receptor for oxidized LDL on endothelial cells, macrophages, smooth muscle cells,[7] and other cell types.[8] But minimally oxidized LDL is more readily recognized by the TLR4 receptor, and highly oxidized LDL is more readily recognized by the CD36 receptor.[9]

Function

LOX-1 is a receptor protein which belongs to the C-type lectin superfamily. Its gene is regulated through the cyclic AMP signaling pathway. The protein binds, internalizes and degrades oxidized low-density lipoprotein.

Normally, LOX-1 expression on endothelial cells is low, but tumor necrosis factor alpha, oxidized LDL, blood vessel sheer stress, and other atherosclerotic stimuli substantially increase LOX-1 expression.[8][10]

LOX-1 may be involved in the regulation of Fas-induced apoptosis. Oxidized LDL induces endothelial cell apoptosis through LOX-1 binding.[7] Other ligands for LOX-1 include oxidized high-density lipoprotein, advanced glycation end-products, platelets, and apoptotic cells.[7][10] The binding of platelets to LOX-1 causes a release of vasoconstrictive endothelin, which induces endothelial dysfunction.[10]

This protein may play a role as a scavenger receptor.[6]

Clinical significance

Binding of oxidized LDL to LOX-1 activates NF-κB, leading to monocyte adhesion to enthothelial cells (a pre-requisite for the macrophage foam cell formation of atherosclerosis).[8] Macrophage affinity for unmodified LDL particles is low, but is greatly increased when the LDL particles are oxidized.[11] LDL oxidation occurs in the sub-endothelial space, rather than in the circulation.[11] But oxidized cholesterol from foods cooked at high temperature can also be a source of oxysterols.[9]

Mutations of the OLR1 gene have been associated with atherosclerosis, risk of myocardial infarction, and may modify the risk of Alzheimer's disease.[6] When applied to human macrophage-derived foam cells in vitro, the dietary supplement berberine inhibits the expression of the ORL1 gene in response to oxidized low-density lipoprotein cholesterol,[12] but this has not yet been demonstrated in a living animal or human.

gollark: The average person really does not want to do anything remotely complicated with a computer, which is problematic, and it doesn't really *help* that a bunch of stuff (down to the balance of upload/download speeds available on home network connections) on the internet is set up now to encourage using big walled gardens and discourage running your own stuff.
gollark: Well, you can't easily, which is the problem.
gollark: Because it's run by a bunch of individuals or smaller groups and can be networked together.
gollark: Which is why I like self-hostable/federated stuff.
gollark: It's not hard technologically. It's hard to make people move.

References
  1. GRCh38: Ensembl release 89: ENSG00000173391 - Ensembl, May 2017
  2. GRCm38: Ensembl release 89: ENSMUSG00000030162 - Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. Li X, Bouzyk MM, Wang X (Nov 1998). "Assignment of the human oxidized low-density lipoprotein receptor gene (OLR1) to chromosome 12p13.1→p12.3, and identification of a polymorphic CA-repeat marker in the OLR1 gene". Cytogenet Cell Genet. 82 (1–2): 34–6. doi:10.1159/000015059. PMID 9763655.
  6. "Entrez Gene: OLR1 oxidized low density lipoprotein (lectin-like) receptor 1".
  7. Pirillo A, Norata GD, Catapano AL (2013). "LOX-1, OxLDL, and atherosclerosis". Mediators of Inflammation. 2013: 1–12. doi:10.1155/2013/152786. PMC 3723318. PMID 23935243.
  8. Xu S, Ogura S, Chen J, Little PJ, Moss J, Liu P (2013). "LOX-1 in atherosclerosis: biological functions and pharmacological modifiers". Cellular and Molecular Life Sciences. 70 (16): 2859–2872. doi:10.1007/s00018-012-1194-z. PMC 4142049. PMID 23124189.
  9. Zmysłowski A, Szterk A (2017). "Current knowledge on the mechanism of atherosclerosis and pro-atherosclerotic properties of oxysterols". Lipids in Health and Disease. 16 (1): 188. doi:10.1186/s12944-017-0579-2. PMC 5625595. PMID 28969682.
  10. Kakutani M, Masaki T, Sawamura T (2000). "A platelet-endothelium interaction mediated by lectin-like oxidized low-density lipoprotein receptor-1". Proceedings of the National Academy of Sciences of the United States of America. 97 (1): 360–364. Bibcode:2000PNAS...97..360K. doi:10.1016/j.biochi.2016.10.010. PMC 26668. PMID 10618423.
  11. Brites F, Martin M, Guillas I, Kontush A (2017). "Antioxidative activity of high-density lipoprotein (HDL): Mechanistic insights into potential clinical benefit". BBA Clinical. 8: 66–77. doi:10.1016/j.bbacli.2017.07.002. PMC 5597817. PMID 28936395.
  12. Guan S, Wang B, Li W, Guan J, Fang X (2010). "Effects of berberine on expression of LOX-1 and SR-BI in human macrophage-derived foam cells induced by ox-LDL". Am J Chin Med. 38 (6): 1161–9. doi:10.1142/s0192415x10008548. PMID 21061468.

Further reading
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.