CCL4

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Hemokin (C-C motiv) ligand 4

PDB prikaz baziran na 1hum.
Dostupne strukture
1hum, 1hun, 1je4, 2ffk, 2fin
Identifikatori
SimboliCCL4; SCYA4; ACT2; AT744.1; G-26; LAG1; MGC104418; MGC126025; MGC126026; MIP-1-beta; MIP1B
Vanjski IDOMIM: 182284 MGI: 98261 HomoloGene: 48153 GeneCards: CCL4 Gene
Ontologija gena
Molekularna funkcija aktivnost receptor signalne protein tyrozin kinaze
hemokinska aktivnost
Celularna komponenta ekstracelularni region
ekstracelularni prostor
Biološki proces ćelijska pokretljivost
hemotaksa
inflamatorni respons
imunski respons
ćelijska adhezija
uspostavljanje i/ili održavanje ćelijske polarnosti
prenos signala
interćelijska signalizacija
respons na viruse
replikacija viralnog genoma
Pregled RNK izražavanja
podaci
Ortolozi
VrstaČovekMiš
Entrez635120303
EnsemblENSG00000129277ENSMUSG00000018930
UniProtP13236Q5QNV9
RefSeq (mRNA)NM_002984NM_013652
RefSeq (protein)NP_002975NP_038680
Lokacija (UCSC)Chr 17:
31.46 - 31.46 Mb
Chr 11:
83.48 - 83.48 Mb
PubMed pretraga[1][2]

CCL4, hemokin (C-C motiv) ligand 4, je protein koji je kod ljudi kodiran CCL4 genom.[1][2]

Funkcija

CCL4 je CC chemokin koji je specifičan za CCR5 receptore. On je hemoatraktant za NK ćelije, monocite i niz drugih imunskih ćelija.[3]

CCL4 je značajan HIV-supresujući faktor koji proizvode CD8+ T ćelije.[4] Perforin memorijske CD8+ T ćelije normalno sintetišu MIP-1-beta.[5]

Interakcije

Za CCL4 je bilo pokazano da interaguje sa CCL3.[6]

Vidi još

  • Macrofag inflamatorni protein

Reference

  1. Irving SG, Zipfel PF, Balke J, McBride OW, Morton CC, Burd PR, Siebenlist U, Kelly K (June 1990). „Two inflammatory mediator cytokine genes are closely linked and variably amplified on chromosome 17q”. Nucleic Acids Res. 18 (11): 3261–70. DOI:10.1093/nar/18.11.3261. PMC 330932. PMID 1972563. 
  2. Mire-Sluis, Anthony R.; Thorpe, Robin, ur. (1998). Cytokines (Handbook of Immunopharmacology). Boston: Academic Press. ISBN 0-12-498340-5. 
  3. Bystry RS, Aluvihare V, Welch KA, Kallikourdis M, Betz AG (December 2001). „B cells and professional APCs recruit regulatory T cells via CCL4”. Nat. Immunol. 2 (12): 1126–32. DOI:10.1038/ni735. PMID 11702067. 
  4. Cocchi F, DeVico AL, Garzino-Demo A, Arya SK, Gallo RC, Lusso P (December 1995). „Identification of RANTES, MIP-1 alpha, and MIP-1 beta as the major HIV-suppressive factors produced by CD8+ T cells”. Science (journal) 270 (5243): 1811–5. PMID 8525373. 
  5. Kamin-Lewis R, Abdelwahab SF, Trang C, Baker A, DeVico AL, Gallo RC, Lewis GK (July 2001). „Perforin-low memory CD8+ cells are the predominant T cells in normal humans that synthesize the beta -chemokine macrophage inflammatory protein-1beta”. Proc. Natl. Acad. Sci. U.S.A. 98 (16): 9283–8. DOI:10.1073/pnas.161298998. PMC 55412. PMID 11470920. 
  6. Guan, E; Wang J, Norcross M A (April 2001). „Identification of human macrophage inflammatory proteins 1alpha and 1beta as a native secreted heterodimer”. J. Biol. Chem. (United States) 276 (15): 12404–9. DOI:10.1074/jbc.M006327200. ISSN 0021-9258. PMID 11278300. 

Literatura

  • Menten P, Wuyts A, Van Damme J (2002). „Macrophage inflammatory protein-1.”. Cytokine Growth Factor Rev. 13 (6): 455–81. DOI:10.1016/S1359-6101(02)00045-X. PMID 12401480. 
  • Muthumani K, Desai BM, Hwang DS, et al. (2004). „HIV-1 Vpr and anti-inflammatory activity.”. DNA Cell Biol. 23 (4): 239–47. DOI:10.1089/104454904773819824. PMID 15142381. 
  • Conti L, Fantuzzi L, Del Cornò M, et al. (2005). „Immunomodulatory effects of the HIV-1 gp120 protein on antigen presenting cells: implications for AIDS pathogenesis.”. Immunobiology 209 (1-2): 99–115. DOI:10.1016/j.imbio.2004.02.008. PMID 15481145. 
  • Joseph AM, Kumar M, Mitra D (2005). „Nef: "necessary and enforcing factor" in HIV infection.”. Curr. HIV Res. 3 (1): 87–94. DOI:10.2174/1570162052773013. PMID 15638726. 
  • Zhao RY, Elder RT (2005). „Viral infections and cell cycle G2/M regulation.”. Cell Res. 15 (3): 143–9. DOI:10.1038/sj.cr.7290279. PMID 15780175. 
  • Zhao RY, Bukrinsky M, Elder RT (2005). „HIV-1 viral protein R (Vpr) & host cellular responses.”. Indian J. Med. Res. 121 (4): 270–86. PMID 15817944. 
  • Li L, Li HS, Pauza CD, et al. (2006). „Roles of HIV-1 auxiliary proteins in viral pathogenesis and host-pathogen interactions.”. Cell Res. 15 (11-12): 923–34. DOI:10.1038/sj.cr.7290370. PMID 16354571. 
  • King JE, Eugenin EA, Buckner CM, Berman JW (2006). „HIV tat and neurotoxicity.”. Microbes Infect. 8 (5): 1347–57. DOI:10.1016/j.micinf.2005.11.014. PMID 16697675. 
  • Napolitano M, Modi WS, Cevario SJ, et al. (1991). „The gene encoding the Act-2 cytokine. Genomic structure, HTLV-I/Tax responsiveness of 5' upstream sequences, and chromosomal localization.”. J. Biol. Chem. 266 (26): 17531–6. PMID 1894635. 
  • Irving SG, Zipfel PF, Balke J, et al. (1990). „Two inflammatory mediator cytokine genes are closely linked and variably amplified on chromosome 17q.”. Nucleic Acids Res. 18 (11): 3261–70. DOI:10.1093/nar/18.11.3261. PMC 330932. PMID 1972563. 
  • Baixeras E, Roman-Roman S, Jitsukawa S, et al. (1991). „Cloning and expression of a lymphocyte activation gene (LAG-1).”. Mol. Immunol. 27 (11): 1091–102. DOI:10.1016/0161-5890(90)90097-J. PMID 2247088. 
  • Lipes MA, Napolitano M, Jeang KT, et al. (1989). „Identification, cloning, and characterization of an immune activation gene.”. Proc. Natl. Acad. Sci. U.S.A. 85 (24): 9704–8. DOI:10.1073/pnas.85.24.9704. PMC 282843. PMID 2462251. 
  • Brown KD, Zurawski SM, Mosmann TR, Zurawski G (1989). „A family of small inducible proteins secreted by leukocytes are members of a new superfamily that includes leukocyte and fibroblast-derived inflammatory agents, growth factors, and indicators of various activation processes.”. J. Immunol. 142 (2): 679–87. PMID 2521353. 
  • Zipfel PF, Balke J, Irving SG, et al. (1989). „Mitogenic activation of human T cells induces two closely related genes which share structural similarities with a new family of secreted factors.”. J. Immunol. 142 (5): 1582–90. PMID 2521882. 
  • Chang HC, Reinherz EL (1989). „Isolation and characterization of a cDNA encoding a putative cytokine which is induced by stimulation via the CD2 structure on human T lymphocytes.”. Eur. J. Immunol. 19 (6): 1045–51. DOI:10.1002/eji.1830190614. PMID 2568930. 
  • Miller MD, Hata S, De Waal Malefyt R, Krangel MS (1989). „A novel polypeptide secreted by activated human T lymphocytes.”. J. Immunol. 143 (9): 2907–16. PMID 2809212. 
  • Adams MD, Kerlavage AR, Fleischmann RD, et al. (1995). „Initial assessment of human gene diversity and expression patterns based upon 83 million nucleotides of cDNA sequence.”. Nature 377 (6547 Suppl): 3–174. PMID 7566098. 
  • Post TW, Bozic CR, Rothenberg ME, et al. (1995). „Molecular characterization of two murine eosinophil beta chemokine receptors.”. J. Immunol. 155 (11): 5299–305. PMID 7594543. 
  • Combadiere C, Ahuja SK, Murphy PM (1995). „Cloning and functional expression of a human eosinophil CC chemokine receptor.”. J. Biol. Chem. 270 (28): 16491–4. DOI:10.1074/jbc.270.28.16491. PMID 7622448. 
  • Paolini JF, Willard D, Consler T, et al. (1994). „The chemokines IL-8, monocyte chemoattractant protein-1, and I-309 are monomers at physiologically relevant concentrations.”. J. Immunol. 153 (6): 2704–17. PMID 8077676. 

Spoljašnje veze

  • CCL4 GeneCard
  • p
  • r
  • u
PDB Galerija
Šablon:PDB Galerija/6351
  • p
  • r
  • u
Po familiji
IL-1 superfamilija
1 (1Ra) • 18 • 33
poput IL-6/gp130 koristeći
IL-10 familija
10 • 19 • 20 • 22 • 24 • 26
28 • 29
2/15 • 3 • 4 • 7 • 9 • 13 • 21
IL-12 familija
12 (B) • 23 • 27 • 35
Drugi
5 • 8 • 14 • 16 • 17/25 (A) • 32  • 34
CCL
1 • 2 • 3 • 4 • 5 • 6 • 7 • 8 • 9 • 10 • 11 • 12 • 13 • 14 • 15 • 16 • 17 • 18 • 19 • 20 • 21 • 22 • 23 • 24 • 25 • 26 • 27 • 28
CXCL
1 • 2 • 3 • 4 • 5 • 6 • 7 • 8 • 9 • 10 • 11 • 12 • 13 • 14 • 15 • 16 • 17
CX3CL
XCL
1 • 2
Glavni
TNF (ligand) superfamilija
CD70 • CD153 • CD154
alfa ( Pegilirani 2a, Pegilirani 2b), beta (1a, 1b)
Drugi
Po funkciji
B trdu: peptidi (nrpl/grfl/cytl/horl), receptori (lgic, enzr, gprc, igsr, intg, nrpr/grfr/cytr), itra (adap, gbpr, mapk), calc, lipd, signalni putevi (hedp, wntp, tgfp+mapp, notp, jakp, fsap, hipp, tlrp)