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MSR1

From Wikipedia, the free encyclopedia
Protein-coding gene in the species Homo sapiens
MSR1
Identifiers
AliasesMSR1, CD204, SCARA1, SR-A, SRA, phSR1, phSR2, macrophage scavenger receptor 1, SR-AI, SR-AII, SR-AIII
External IDsOMIM:153622;MGI:98257;HomoloGene:12822;GeneCards:MSR1;OMA:MSR1 - orthologs
Gene location (Human)
Chromosome 8 (human)
Chr.Chromosome 8 (human)[1]
Chromosome 8 (human)
Genomic location for MSR1
Genomic location for MSR1
Band8p22Start16,107,878bp[1]
End16,567,490bp[1]
Gene location (Mouse)
Chromosome 8 (mouse)
Chr.Chromosome 8 (mouse)[2]
Chromosome 8 (mouse)
Genomic location for MSR1
Genomic location for MSR1
Band8 A4|8 23.89 cMStart40,034,726bp[2]
End40,095,714bp[2]
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • right lung

  • upper lobe of left lung

  • gallbladder

  • Achilles tendon

  • right coronary artery

  • visceral pleura

  • Descending thoracic aorta

  • monocyte

  • testicle

  • ascending aorta
Top expressed in
  • stroma of bone marrow

  • spermatid

  • molar

  • mesenteric lymph nodes

  • gastrula

  • liver

  • seminiferous tubule

  • left lobe of liver

  • submandibular gland

  • sciatic nerve
More reference expression data
BioGPS




More reference expression data
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo /QuickGO
Orthologs
SpeciesHumanMouse
Entrez

4481

20288

Ensembl

ENSG00000038945

ENSMUSG00000025044

UniProt

P21757

P30204

RefSeq (mRNA)

NM_138716
NM_002445
NM_138715
NM_001363744

NM_001113326
NM_031195

RefSeq (protein)

NP_002436
NP_619729
NP_619730
NP_001350673

NP_001106797
NP_112472

Location (UCSC)Chr 8: 16.11 – 16.57 MbChr 8: 40.03 – 40.1 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Macrophage scavenger receptor 1, also known asMSR1, is aprotein which in humans is encoded by theMSR1gene.[5][6] MSR1 has also been designatedCD204 (cluster of differentiation 204).

Function

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This gene encodes the class Amacrophagescavenger receptors, which include three different types (1, 2, 3) generated by alternative splicing of this gene. These receptors or isoforms are trimeric integral membraneglycoproteins and have been implicated in many macrophage-associated physiological and pathological processes including atherosclerosis,Alzheimer's disease, and host defense. They were thought to be expressed macrophage-specific, but recently shown to be present on different dendritic cells classes, too.[7]

The isoforms type 1 and type 2 are functional receptors and are able to mediate the endocytosis of modifiedlow density lipoproteins (LDLs). The isoform type 3 does not internalize modified LDL (acetyl-LDL) despite having the domain shown to mediate this function in the types 1 and 2 isoforms. It has an altered intracellular processing and is trapped within theendoplasmic reticulum, making it unable to performendocytosis. The isoform type 3 can inhibit the function of isoforms type 1 and type 2 when co-expressed, indicating a dominant negative effect and suggesting a mechanism for regulation of scavenger receptor activity in macrophages.[5]

Biotechnology application

[edit]

Macrophage scavenger receptor has been shown to mediate adhesion of macrophages and other cell lines to tissue culture plastic.[8]

Interactions

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MSR1 has been shown tointeract withHSPA1A.[9]

References

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  1. ^abcGRCh38: Ensembl release 89: ENSG00000038945Ensembl, May 2017
  2. ^abcGRCm38: Ensembl release 89: ENSMUSG00000025044Ensembl, 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. ^ab"Entrez Gene: MSR1 macrophage scavenger receptor 1".
  6. ^Matsumoto A, Naito M, Itakura H, Ikemoto S, Asaoka H, Hayakawa I, Kanamori H, Aburatani H, Takaku F, Suzuki H (December 1990)."Human macrophage scavenger receptors: primary structure, expression, and localization in atherosclerotic lesions".Proc. Natl. Acad. Sci. U.S.A.87 (23):9133–7.Bibcode:1990PNAS...87.9133M.doi:10.1073/pnas.87.23.9133.PMC 55118.PMID 2251254.
  7. ^Herber DL, Cao W, Nefedova Y, Novitskiy SV, Nagaraj S, Tyurin VA, Corzo A, Cho HI, Celis E, Lennox B, Knight SC, Padhya T, McCaffrey TV, McCaffrey JC, Antonia S, Fishman M, Ferris RL, Kagan VE, Gabrilovich DI (August 2010)."Lipid accumulation and dendritic cell dysfunction in cancer".Nat. Med.16 (8):880–6.doi:10.1038/nm.2172.PMC 2917488.PMID 20622859.
  8. ^Robbins AK, Horlick RA (August 1998)."Macrophage scavenger receptor confers an adherent phenotype to cells in culture".BioTechniques.25 (2):240–4.doi:10.2144/98252st04.PMID 9714883.
  9. ^Nakamura, Toshinobu; Hinagata Jun-ichi; Tanaka Toshiki; Imanishi Takeshi; Wada Youichiro; Kodama Tatsuhiko; Doi Takefumi (Jan 2002). "HSP90, HSP70, and GAPDH directly interact with the cytoplasmic domain of macrophage scavenger receptors".Biochem. Biophys. Res. Commun.290 (2). United States:858–64.Bibcode:2002BBRC..290..858N.doi:10.1006/bbrc.2001.6271.ISSN 0006-291X.PMID 11785981.

Further reading

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This article incorporates text from theUnited States National Library of Medicine, which is in thepublic domain.

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