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CXCR3

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维基百科,自由的百科全书
CXCR3
識別號
别名CXCR3;, CD183, CKR-L2, CMKAR3, GPR9, IP10-R, Mig-R, MigR, C-X-C motif chemokine receptor 3, CD182
外部IDOMIM300574 MGI1277207 HomoloGene1153 GeneCardsCXCR3
基因位置(人类
X染色體
染色体X染色體[1]
X染色體
CXCR3的基因位置
CXCR3的基因位置
基因座Xq13.1起始71,615,916 bp[1]
终止71,618,511 bp[1]
RNA表达模式


查阅更多表达数据
直系同源
物種人類小鼠
Entrez
Ensembl
UniProt
mRNA​序列

​NM_001142797
​NM_001504

NM_009910

蛋白序列

NP_001136269
​NP_001495

NP_034040

基因位置​(UCSC)Chr X: 71.62 – 71.62 MbChr X: 100.78 – 100.78 Mb
PubMed​查找[3][4]
維基數據
檢視/編輯人類檢視/編輯小鼠

趋化因子受体CXCR3是G蛋白偶连的七跨膜域受体,可选择性地与CXC趋化因子CXCL9CXCL10,和CXCL11)结合[5]。 CXCR3又称G蛋白偶联受体9(GPR9)和CD183。有两种变异的CXCR3受体。CXCR3-A与CXCL9, CXCL10,CXCL11结合;而CXCR3-B除了与CXCL9, CXCL10,CXCL11结合外还可以与CXCL4结合[6]

表达

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CXCR3主要表达在T细胞自然杀伤细胞活性上[7],有的上皮细胞和一些内皮细胞也表达CXCR3。 I型辅助T细胞(Th1)优先表达CXCR3及CCR5[7],而II型辅助T细胞(Th2)表达CCR3CCR4。 CXCR3与配体结合后在诱导I型辅助T细胞(Th1)迁移的同时又阻止II型辅助T细胞(Th2)的迁徙。从而增强T细胞的分化效应。

信号传递

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CXCR3与其配体CXCL9, CXCL10,CXCL11的结合,能引起细胞钙离子的内流,启动肌醇磷脂3-激酶和丝裂原活化蛋白激酶(MAPK)[8]。详细的信号通路尚未确立,但与其他的趋化因子受体的信号传递有类似的激酶。

功能

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CXCR3调节白细胞迁徙。CXCR3与配体相互作用引起I型辅助T细胞(Th1)的迁移,并促进I型辅助T细胞(Th1)成熟。

疾病

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CXCR3可能在下列疾病中起作用,包括动脉粥样硬化[9]多发性硬化[10]肺纤维化[11]、I型糖尿病[12]、重症肌无力、急性心脏移植排斥[13]。开发阻断CXCR3与其配体相互作用的药物可提供治疗这些疾病的新途径。

参见

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参考文献

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  1. ^ 1.0 1.1 1.2 GRCh38: Ensembl release 89: ENSG00000186810 - Ensembl, May 2017
  2. ^ 2.0 2.1 2.2 GRCm38: Ensembl release 89: ENSMUSG00000050232 - 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. ^ Clark-Lewis, Ian; Mattioli, Ivan; Gong, Jiang-Hong; Loetscher, Pius. Structure-function relationship between the human chemokine receptor CXCR3 and its ligands. The Journal of Biological Chemistry. 2003-01-03, 278 (1): 289–295. ISSN 0021-9258. PMID 12417585. doi:10.1074/jbc.M209470200可免费查阅. 
  6. ^ Lasagni, Laura; Francalanci, Michela; Annunziato, Francesco; Lazzeri, Elena; Giannini, Stefano; Cosmi, Lorenzo; Sagrinati, Costanza; Mazzinghi, Benedetta; Orlando, Claudio; Maggi, Enrico; Marra, Fabio; Romagnani, Sergio; Serio, Mario; Romagnani, Paola. An alternatively spliced variant of CXCR3 mediates the inhibition of endothelial cell growth induced by IP-10, Mig, and I-TAC, and acts as functional receptor for platelet factor 4. The Journal of Experimental Medicine. 2003-06-02, 197 (11): 1537–1549. ISSN 0022-1007. PMC 2193908可免费查阅. PMID 12782716. doi:10.1084/jem.20021897可免费查阅. 
  7. ^ 7.0 7.1 Qin, S.; Rottman, J. B.; Myers, P.; Kassam, N.; Weinblatt, M.; Loetscher, M.; Koch, A. E.; Moser, B.; Mackay, C. R. The chemokine receptors CXCR3 and CCR5 mark subsets of T cells associated with certain inflammatory reactions. The Journal of Clinical Investigation. 1998-02-15, 101 (4): 746–754. ISSN 0021-9738. PMC 508621可免费查阅. PMID 9466968. doi:10.1172/JCI1422可免费查阅. 
  8. ^ Smit, Martine J.; Verdijk, Pauline; van der Raaij-Helmer, Elisabeth M. H.; Navis, Marjon; Hensbergen, Paul J.; Leurs, Rob; Tensen, Cornelis P. CXCR3-mediated chemotaxis of human T cells is regulated by a Gi- and phospholipase C-dependent pathway and not via activation of MEK/p44/p42 MAPK nor Akt/PI-3 kinase. Blood. 2003-09-15, 102 (6): 1959–1965. ISSN 0006-4971. PMID 12750173. doi:10.1182/blood-2002-12-3945. 
  9. ^ Mach, F.; Sauty, A.; Iarossi, A. S.; Sukhova, G. K.; Neote, K.; Libby, P.; Luster, A. D. Differential expression of three T lymphocyte-activating CXC chemokines by human atheroma-associated cells. The Journal of Clinical Investigation. 1999, 104 (8): 1041–1050. ISSN 0021-9738. PMC 408576可免费查阅. PMID 10525042. doi:10.1172/JCI6993可免费查阅. 
  10. ^ Sørensen, T. L.; Tani, M.; Jensen, J.; Pierce, V.; Lucchinetti, C.; Folcik, V. A.; Qin, S.; Rottman, J.; Sellebjerg, F.; Strieter, R. M.; Frederiksen, J. L.; Ransohoff, R. M. Expression of specific chemokines and chemokine receptors in the central nervous system of multiple sclerosis patients. The Journal of Clinical Investigation. 1999, 103 (6): 807–815. ISSN 0021-9738. PMC 408141可免费查阅. PMID 10079101. doi:10.1172/JCI5150可免费查阅. 
  11. ^ Jiang, Dianhua; Liang, Jiurong; Hodge, Jennifer; Lu, Bao; Zhu, Zhou; Yu, Shuang; Fan, Juan; Gao, Yunfei; Yin, Zhinan; Homer, Robert; Gerard, Craig; Noble, Paul W. Regulation of pulmonary fibrosis by chemokine receptor CXCR3. The Journal of Clinical Investigation. 2004, 114 (2): 291–299. ISSN 0021-9738. PMC 449741可免费查阅. PMID 15254596. doi:10.1172/JCI16861可免费查阅. 
  12. ^ Frigerio, Simona; Junt, Tobias; Lu, Bao; Gerard, Craig; Zumsteg, Urs; Holländer, Georg A.; Piali, Luca. Beta cells are responsible for CXCR3-mediated T-cell infiltration in insulitis. Nature Medicine. 2002, 8 (12): 1414–1420. ISSN 1078-8956. PMID 12415259. doi:10.1038/nm1202-792. 
  13. ^ Hancock, W. W.; Lu, B.; Gao, W.; Csizmadia, V.; Faia, K.; King, J. A.; Smiley, S. T.; Ling, M.; Gerard, N. P.; Gerard, C. Requirement of the chemokine receptor CXCR3 for acute allograft rejection. The Journal of Experimental Medicine. 2000-11-20, 192 (10): 1515–1520. ISSN 0022-1007. PMC 2193193可免费查阅. PMID 11085753. doi:10.1084/jem.192.10.1515可免费查阅. 

外部链接

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