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Colony stimulating factor 1 receptor

 
Wikipedia: Colony stimulating factor 1 receptor
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Colony stimulating factor 1 receptor, formerly McDonough feline sarcoma viral (v-fms) oncogene homolog
Identifiers
Symbols CSF1R; C-FMS; CD115; CSFR; FIM2; FMS
External IDs OMIM: 164770 MGI1339758 HomoloGene3817
RNA expression pattern

More reference expression data

Orthologs
Human Mouse
Entrez 1436 12978
Ensembl ENSG00000182578 ENSMUSG00000024621
Uniprot P07333 Q0P635
Refseq NM_005211 (mRNA)
NP_005202 (protein)
NM_001037859 (mRNA)
NP_001032948 (protein)
Location Chr 5: 149.41 - 149.47 Mb Chr 18: 61.23 - 61.26 Mb
Pubmed search [1] [2]

Colony stimulating factor 1 receptor (CSF1R), also known as macrophage colony-stimulating factor receptor (M-CFSR), and CD115 (Cluster of Differentiation 115), is a cell-surface protein encoded, in humans, by the CSF1R gene.[1][2] It is a receptor for a cytokine called colony stimulating factor 1.

Contents

Function

The protein encoded by the CSFR1 gene is the receptor for colony stimulating factor 1, a cytokine which controls the production, differentiation, and function of macrophages. This receptor mediates most, if not all, of the biological effects of this cytokine. Ligand binding activates CSFR1 through a process of oligomerization and transphosphorylation. The encoded protein is a tyrosine kinase transmembrane receptor and member of the CSF1/PDGF receptor family of tyrosine-protein kinases. The first intron of the CSFR1 gene contains a transcriptionally inactive ribosomal protein L7 processed pseudogene, oriented in the opposite direction to the CSFR1 gene.[1]

Clinical significance

Mutations in CSF1R are associated with chronic myelomonocytic leukemia and type M4 acute myeloblastic leukemia.[3] Increased levels of CSF1R1 are found in microglia in Alzheimer's disease and after brain injuries. The increased receptor expression causes microglia to become more active.[4]

Interactions

Colony stimulating factor 1 receptor has been shown to interact with FYN,[5] Suppressor of cytokine signaling 1,[6] Grb2[7] and Cbl gene.[8]

See also

References

  1. ^ a b "Entrez Gene: CSF1R colony stimulating factor 1 receptor, formerly McDonough feline sarcoma viral (v-fms) oncogene homolog". http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=1436. 
  2. ^ Galland F, Stefanova M, Lafage M, Birnbaum D (1992). "Localization of the 5' end of the MCF2 oncogene to human chromosome 15q15----q23". Cytogenet. Cell Genet. 60 (2): 114–6. doi:10.1159/000133316. PMID 1611909. 
  3. ^ Ridge SA, Worwood M, Oscier D, Jacobs A, Padua RA (February 1990). "FMS mutations in myelodysplastic, leukemic, and normal subjects". Proc. Natl. Acad. Sci. U.S.A. 87 (4): 1377–80. doi:10.1073/pnas.87.4.1377. PMID 2406720. PMC: 53478. http://www.pnas.org/cgi/pmidlookup?view=long&pmid=2406720. 
  4. ^ Mitrasinovic OM, Grattan A, Robinson CC, Lapustea NB, Poon C, Ryan H, Phong C, Murphy GM (April 2005). "Microglia overexpressing the macrophage colony-stimulating factor receptor are neuroprotective in a microglial-hippocampal organotypic coculture system". J. Neurosci. 25 (17): 4442–51. doi:10.1523/JNEUROSCI.0514-05.2005. PMID 15858070. 
  5. ^ Courtneidge, S A; Dhand R, Pilat D, Twamley G M, Waterfield M D, Roussel M F (Mar. 1993). "Activation of Src family kinases by colony stimulating factor-1, and their association with its receptor". EMBO J. (ENGLAND) 12 (3): 943-50. ISSN 0261-4189. PMID 7681396. 
  6. ^ Bourette, R P; De Sepulveda P, Arnaud S, Dubreuil P, Rottapel R, Mouchiroud G (Jun. 2001). "Suppressor of cytokine signaling 1 interacts with the macrophage colony-stimulating factor receptor and negatively regulates its proliferation signal". J. Biol. Chem. (United States) 276 (25): 22133-9. doi:10.1074/jbc.M101878200. ISSN 0021-9258. PMID 11297560. 
  7. ^ Mancini, A; Niedenthal R, Joos H, Koch A, Trouliaris S, Niemann H, Tamura T (Sep. 1997). "Identification of a second Grb2 binding site in the v-Fms tyrosine kinase". Oncogene (ENGLAND) 15 (13): 1565-72. doi:10.1038/sj.onc.1201518. ISSN 0950-9232. PMID 9380408. 
  8. ^ Mancini, Annalisa; Koch Alexandra, Wilms Regina, Tamura Teruko (Apr. 2002). "c-Cbl associates directly with the C-terminal tail of the receptor for the macrophage colony-stimulating factor, c-Fms, and down-modulates this receptor but not the viral oncogene v-Fms". J. Biol. Chem. (United States) 277 (17): 14635-40. doi:10.1074/jbc.M109214200. ISSN 0021-9258. PMID 11847211. 

Further reading

  • Rettenmier CW, Roussel MF, Sherr CJ (1989). "The colony-stimulating factor 1 (CSF-1) receptor (c-fms proto-oncogene product) and its ligand.". J. Cell Sci. Suppl. 9: 27–44. PMID 2978516. 
  • Stanley ER, Berg KL, Einstein DB, et al. (1997). "Biology and action of colony--stimulating factor-1.". Mol. Reprod. Dev. 46 (1): 4–10. doi:10.1002/(SICI)1098-2795(199701)46:1<4::AID-MRD2>3.0.CO;2-V. PMID 8981357. 
  • Gout I, Dhand R, Panayotou G, et al. (1993). "Expression and characterization of the p85 subunit of the phosphatidylinositol 3-kinase complex and a related p85 beta protein by using the baculovirus expression system.". Biochem. J. 288 ( Pt 2): 395–405. PMID 1334406. 
  • Galland F, Stefanova M, Lafage M, Birnbaum D (1992). "Localization of the 5' end of the MCF2 oncogene to human chromosome 15q15----q23.". Cytogenet. Cell Genet. 60 (2): 114–6. doi:10.1159/000133316. PMID 1611909. 
  • Boultwood J, Rack K, Kelly S, et al. (1991). "Loss of both CSF1R (FMS) alleles in patients with myelodysplasia and a chromosome 5 deletion.". Proc. Natl. Acad. Sci. U.S.A. 88 (14): 6176–80. doi:10.1073/pnas.88.14.6176. PMID 1829836. 
  • Roussel MF, Cleveland JL, Shurtleff SA, Sherr CJ (1991). "Myc rescue of a mutant CSF-1 receptor impaired in mitogenic signalling.". Nature 353 (6342): 361–3. doi:10.1038/353361a0. PMID 1833648. 
  • Reedijk M, Liu XQ, Pawson T (1990). "Interactions of phosphatidylinositol kinase, GTPase-activating protein (GAP), and GAP-associated proteins with the colony-stimulating factor 1 receptor.". Mol. Cell. Biol. 10 (11): 5601–8. PMID 2172781. 
  • Ridge SA, Worwood M, Oscier D, et al. (1990). "FMS mutations in myelodysplastic, leukemic, and normal subjects.". Proc. Natl. Acad. Sci. U.S.A. 87 (4): 1377–80. doi:10.1073/pnas.87.4.1377. PMID 2406720. 
  • Sherr CJ, Rettenmier CW, Sacca R, et al. (1985). "The c-fms proto-oncogene product is related to the receptor for the mononuclear phagocyte growth factor, CSF-1.". Cell 41 (3): 665–76. doi:10.1016/S0092-8674(85)80047-7. PMID 2408759. 
  • Coussens L, Van Beveren C, Smith D, et al. (1986). "Structural alteration of viral homologue of receptor proto-oncogene fms at carboxyl terminus.". Nature 320 (6059): 277–80. doi:10.1038/320277a0. PMID 2421165. 
  • Hampe A, Shamoon BM, Gobet M, et al. (1989). "Nucleotide sequence and structural organization of the human FMS proto-oncogene.". Oncogene Res. 4 (1): 9–17. PMID 2524025. 
  • Visvader J, Verma IM (1989). "Differential transcription of exon 1 of the human c-fms gene in placental trophoblasts and monocytes.". Mol. Cell. Biol. 9 (3): 1336–41. PMID 2524648. 
  • Roberts WM, Look AT, Roussel MF, Sherr CJ (1988). "Tandem linkage of human CSF-1 receptor (c-fms) and PDGF receptor genes.". Cell 55 (4): 655–61. doi:10.1016/0092-8674(88)90224-3. PMID 2846185. 
  • Xu DQ, Guilhot S, Galibert F (1985). "Restriction fragment length polymorphism of the human c-fms gene.". Proc. Natl. Acad. Sci. U.S.A. 82 (9): 2862–5. doi:10.1073/pnas.82.9.2862. PMID 2986142. 
  • Sherr CJ, Rettenmier CW (1987). "The fms gene and the CSF-1 receptor.". Cancer Surv. 5 (2): 221–32. PMID 3022923. 
  • Le Beau MM, Westbrook CA, Diaz MO, et al. (1986). "Evidence for the involvement of GM-CSF and FMS in the deletion (5q) in myeloid disorders.". Science 231 (4741): 984–7. doi:10.1126/science.3484837. PMID 3484837. 
  • Wheeler EF, Roussel MF, Hampe A, et al. (1986). "The amino-terminal domain of the v-fms oncogene product includes a functional signal peptide that directs synthesis of a transforming glycoprotein in the absence of feline leukemia virus gag sequences.". J. Virol. 59 (2): 224–33. PMID 3525854. 
  • Browning PJ, Bunn HF, Cline A, et al. (1986). ""Replacement" of COOH-terminal truncation of v-fms with c-fms sequences markedly reduces transformation potential.". Proc. Natl. Acad. Sci. U.S.A. 83 (20): 7800–4. doi:10.1073/pnas.83.20.7800. PMID 3532121. 
  • Verbeek JS, Roebroek AJ, van den Ouweland AM, et al. (1985). "Human c-fms proto-oncogene: comparative analysis with an abnormal allele.". Mol. Cell. Biol. 5 (2): 422–6. PMID 3974576. 

External links

This article incorporates text from the United States National Library of Medicine, which is in the public domain.



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