CCL17

edit
Hemokin (C-C motiv) ligand 17

PDB prikaz baziran na 1nr2.
Dostupne strukture
1nr2, 1nr4
Identifikatori
SimboliCCL17; A-152E5.3; ABCD-2; MGC138271; MGC138273; SCYA17; TARC
Vanjski IDOMIM: 601520 MGI: 1329039 HomoloGene: 2246 GeneCards: CCL17 Gene
Ontologija gena
Molekularna funkcija • hemokinska aktivnost
Celularna komponenta • ekstracelularni region
• ekstracelularni prostor
Biološki proces • hemotaksa
• inflamatorni odgovor
• imunski odgovor
• G-protein spregnuti receptor proteinski signalni put
• interćelijska signalizacija
• razvoj multicelularnih organizama
Pregled RNK izražavanja
podaci
Ortolozi
VrstaČovekMiš
Entrez636120295
EnsemblENSG00000102970ENSMUSG00000031780
UniProtQ92583n/a
RefSeq (mRNA)NM_002987NM_011332
RefSeq (protein)NP_002978NP_035462
Lokacija (UCSC)Chr 16:
56.01 - 56.01 Mb		Chr 8:
97.7 - 97.7 Mb
PubMed pretraga[1][2]

CCL17, hemokin (C-C motiv) ligand 17, je mali citokin iz CC hemokin familije koji je takođe poznat kao timusom i activacijom regulisani hemokin (TARC). CCL17 je izražen konstitutivno u timusu, ali samo tranzijentno u fitohemaglutinin-stimulisanim perifernim krvnim mononuklearnim ćelijama.[1] Ovaj hemokin se specifično vezuje i indukuje hemotaksu u T ćelijama. On dejstvuje putem interakcija sa hemokin receptorom CCR4.[1][2] Gen za CCL17 je lociran na hromozomu 16 kod ljudi, zajedno sa hemokinima CCL22 i CX3CL1.[3][4][5]

Reference

  1. ↑ 1,0 1,1 Imai T, Yoshida T, Baba M, Nishimura M, Kakizaki M, Yoshie O (1996). „Molecular cloning of a novel T cell-directed CC chemokine expressed in thymus by signal sequence trap using Epstein-Barr virus vector”. J. Biol. Chem. 271 (35): 21514–21. DOI:10.1074/jbc.271.35.21514. PMID 8702936. 
  2. ↑ Imai T, Baba M, Nishimura M, Kakizaki M, Takagi S, Yoshie O (1997). „The T cell-directed CC chemokine TARC is a highly specific biological ligand for CC chemokine receptor 4”. J. Biol. Chem. 272 (23): 15036–42. DOI:10.1074/jbc.272.23.15036. PMID 9169480. 
  3. ↑ Nomiyama H, Imai T, Kusuda J, Miura R, Callen DF, Yoshie O (1997). „Assignment of the human CC chemokine gene TARC (SCYA17) to chromosome 16q13”. Genomics 40 (1): 211–3. DOI:10.1006/geno.1996.4552. PMID 9070951. 
  4. ↑ Nomiyama H, Imai T, Kusuda J, Miura R, Callen DF, Yoshie O (1998). „Human chemokines fractalkine (SCYD1), MDC (SCYA22) and TARC (SCYA17) are clustered on chromosome 16q13”. Cytogenet. Cell Genet. 81 (1): 10–1. DOI:10.1159/000015000. PMID 9691168. 
  5. ↑ Mire-Sluis, Anthony R.; Thorpe, Robin, ur. (1998). Cytokines (Handbook of Immunopharmacology). Boston: Academic Press. ISBN 0-12-498340-5. 

Literatura

  • Saeki H, Tamaki K (2006). „Thymus and activation regulated chemokine (TARC)/CCL17 and skin diseases.”. J. Dermatol. Sci. 43 (2): 75–84. DOI:10.1016/j.jdermsci.2006.06.002. PMID 16859899. 
  • Imai T, Yoshida T, Baba M, et al. (1996). „Molecular cloning of a novel T cell-directed CC chemokine expressed in thymus by signal sequence trap using Epstein-Barr virus vector.”. J. Biol. Chem. 271 (35): 21514–21. DOI:10.1074/jbc.271.35.21514. PMID 8702936. 
  • Nomiyama H, Imai T, Kusuda J, et al. (1997). „Assignment of the human CC chemokine gene TARC (SCYA17) to chromosome 16q13.”. Genomics 40 (1): 211–3. DOI:10.1006/geno.1996.4552. PMID 9070951. 
  • Imai T, Baba M, Nishimura M, et al. (1997). „The T cell-directed CC chemokine TARC is a highly specific biological ligand for CC chemokine receptor 4.”. J. Biol. Chem. 272 (23): 15036–42. DOI:10.1074/jbc.272.23.15036. PMID 9169480. 
  • Imai T, Chantry D, Raport CJ, et al. (1998). „Macrophage-derived chemokine is a functional ligand for the CC chemokine receptor 4.”. J. Biol. Chem. 273 (3): 1764–8. DOI:10.1074/jbc.273.3.1764. PMID 9430724. 
  • Bernardini G, Hedrick J, Sozzani S, et al. (1998). „Identification of the CC chemokines TARC and macrophage inflammatory protein-1 beta as novel functional ligands for the CCR8 receptor.”. Eur. J. Immunol. 28 (2): 582–8. DOI:10.1002/(SICI)1521-4141(199802)28:02<582::AID-IMMU582>3.0.CO;2-A. PMID 9521068. 
  • Nomiyama H, Imai T, Kusuda J, et al. (1998). „Human chemokines fractalkine (SCYD1), MDC (SCYA22) and TARC (SCYA17) are clustered on chromosome 16q13.”. Cytogenet. Cell Genet. 81 (1): 10–1. DOI:10.1159/000015000. PMID 9691168. 
  • Struyf S, Proost P, Sozzani S, et al. (1998). „Enhanced anti-HIV-1 activity and altered chemotactic potency of NH2-terminally processed macrophage-derived chemokine (MDC) imply an additional MDC receptor.”. J. Immunol. 161 (6): 2672–5. PMID 9743322. 
  • Loftus BJ, Kim UJ, Sneddon VP, et al. (1999). „Genome duplications and other features in 12 Mb of DNA sequence from human chromosome 16p and 16q.”. Genomics 60 (3): 295–308. DOI:10.1006/geno.1999.5927. PMID 10493829. 
  • Garlisi CG, Xiao H, Tian F, et al. (1999). „The assignment of chemokine-chemokine receptor pairs: TARC and MIP-1 beta are not ligands for human CC-chemokine receptor 8.”. Eur. J. Immunol. 29 (10): 3210–5. DOI:10.1002/(SICI)1521-4141(199910)29:10<3210::AID-IMMU3210>3.0.CO;2-W. PMID 10540332. 
  • Dias Neto E, Correa RG, Verjovski-Almeida S, et al. (2000). „Shotgun sequencing of the human transcriptome with ORF expressed sequence tags.”. Proc. Natl. Acad. Sci. U.S.A. 97 (7): 3491–6. DOI:10.1073/pnas.97.7.3491. PMC 16267. PMID 10737800. 
  • Ghia P, Transidico P, Veiga JP, et al. (2001). „Chemoattractants MDC and TARC are secreted by malignant B-cell precursors following CD40 ligation and support the migration of leukemia-specific T cells.”. Blood 98 (3): 533–40. DOI:10.1182/blood.V98.3.533. PMID 11468146. 
  • Morita A, Kikuoka S, Horikawa T, et al. (2002). „Evaluation of human thymus and activation-regulated chemokine concentrations in blood using a new sandwich ELISA based on monoclonal antibodies.”. Clin. Chim. Acta 322 (1-2): 67–75. DOI:10.1016/S0009-8981(02)00131-6. PMID 12104083. 
  • Basu S, Schaefer TM, Ghosh M, et al. (2003). „Molecular cloning and sequencing of 25 different rhesus macaque chemokine cDNAs reveals evolutionary conservation among C, CC, CXC, AND CX3C families of chemokines.”. Cytokine 18 (3): 140–8. DOI:10.1006/cyto.2002.0875. PMID 12126650. 
  • D'Ambrosio D, Albanesi C, Lang R, et al. (2002). „Quantitative differences in chemokine receptor engagement generate diversity in integrin-dependent lymphocyte adhesion.”. J. Immunol. 169 (5): 2303–12. PMID 12193695. 
  • Matsumoto N, Mukae H, Nakamura-Uchiyama F, et al. (2002). „Elevated levels of thymus and activation-regulated chemokine (TARC) in pleural effusion samples from patients infested with Paragonimus westermani.”. Clin. Exp. Immunol. 130 (2): 314–8. DOI:10.1046/j.1365-2249.2002.01985.x. PMC 1906524. PMID 12390321. 
  • Zheng X, Nakamura K, Tojo M, et al. (2003). „TGF-beta1-mediated regulation of thymus and activation-regulated chemokine (TARC/CCL17) synthesis and secretion by HaCaT cells co-stimulated with TNF-alpha and IFN-gamma.”. J. Dermatol. Sci. 30 (2): 154–60. DOI:10.1016/S0923-1811(02)00071-3. PMID 12413771. 
  • Kakinuma T, Nakamura K, Wakugawa M, et al. (2003). „IL-4, but not IL-13, modulates TARC (thymus and activation-regulated chemokine)/CCL17 and IP-10 (interferon-induced protein of 10kDA)/CXCL10 release by TNF-alpha and IFN-gamma in HaCaT cell line.”. Cytokine 20 (1): 1–6. DOI:10.1006/cyto.2002.1965. PMID 12441140. 
  • Uchida T, Suto H, Ra C, et al. (2003). „Preferential expression of T(h)2-type chemokine and its receptor in atopic dermatitis.”. Int. Immunol. 14 (12): 1431–8. DOI:10.1093/intimm/dxf109. PMID 12456591. 
  • Strausberg RL, Feingold EA, Grouse LH, et al. (2003). „Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.”. Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. DOI:10.1073/pnas.242603899. PMC 139241. PMID 12477932.