Chemokine receptor trafficking and viral replication

被引:67
作者
Pelchen-Matthews, A
Signoret, N
Klasse, PJ
Fraile-Ramos, A
Marsh, M
机构
[1] UCL, MRC, Mol Cell Biol Lab, London WC1E 6BT, England
[2] UCL, Dept Biochem & Mol Biol, London WC1E 6BT, England
关键词
D O I
10.1111/j.1600-065X.1999.tb01281.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Chemokines and chemokine receptors have emerged as crucial factors controlling the development and function of leukocytes, Recent studies have indicated that, in addition to these essential roles, both chemokines and chemokine receptors play critical roles in viral infection and replication. Not only are chemokine receptors key components of the receptor/fusion complexes of primate immunodeficiency viruses, but chemokines can also influence virus entry and infection. Many viruses, in particular herpesviruses, encode chemokines and chemokine receptors that influence the replication of both the parent virus and other unrelated viruses. The cell surface expression of the chemokine receptors is regulated through their interaction with membrane trafficking pathways. Ligands induce receptor internalization and downmodulation through endocytosis, and recycling is regulated within endosomes, Part of the mechanism through which chemokines protect cells from HIV infection is through ligand-induced internalization of the specific chemokine receptor coreceptors. In addition, mechanisms may exist to regulate the trafficking of newly synthesized receptors to the cell surface. Here we discuss aspects of the mechanisms through which chemokine receptors interact with membrane-trafficking pathways and the influence of these interactions on viral replication.
引用
收藏
页码:33 / 49
页数:17
相关论文
共 160 条
[1]  
AHUJA SK, 1993, J BIOL CHEM, V268, P20691
[2]   CC CKRS: A RANTES, MIP-1 alpha, MIP-1 beta receptor as a fusion cofactor for macrophage-tropic HIV-1 [J].
Alkhatib, G ;
Combadiere, C ;
Broder, CC ;
Feng, Y ;
Kennedy, PE ;
Murphy, PM ;
Berger, EA .
SCIENCE, 1996, 272 (5270) :1955-1958
[3]   HIV-1 coreceptor activity of CCR5 and its inhibition by chemokines: Independence from G protein signaling and importance of coreceptor downmodulation [J].
Alkhatib, G ;
Locati, M ;
Kennedy, PE ;
Murphy, PM ;
Berger, EA .
VIROLOGY, 1997, 234 (02) :340-348
[4]   A new SIV co-receptor, STRL33 [J].
Alkhatib, G ;
Liao, F ;
Berger, EA ;
Farber, JM ;
Peden, KWC .
NATURE, 1997, 388 (6639) :238-238
[5]   HIV coreceptor downregulation as antiviral principle: SDF-1 alpha-dependent internalization of the chemokine receptor CXCR4 contributes to inhibition of HIV replication [J].
Amara, A ;
LeGall, S ;
Schwartz, O ;
Salamero, J ;
Montes, M ;
Loetscher, P ;
Baggiolini, M ;
Virelizier, JL ;
ArenzanaSeisdedos, F .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 186 (01) :139-146
[6]   Bound simian virus 40 translocates to caveolin-enriched membrane domains, and its entry is inhibited by drugs that selectively disrupt caveolae [J].
Anderson, HA ;
Chen, YZ ;
Norkin, LC .
MOLECULAR BIOLOGY OF THE CELL, 1996, 7 (11) :1825-1834
[7]   The extent of genetic variation in the CCR5 gene [J].
AnsariLari, MA ;
Liu, XM ;
Metzker, ML ;
Rut, AR ;
Gibbs, RA .
NATURE GENETICS, 1997, 16 (03) :221-222
[8]   Monocyte chemoattractant protein-1-induced CCR2B receptor desensitization mediated by the G protein-coupled receptor kinase 2 [J].
Aragay, AM ;
Mellado, M ;
Frade, JMR ;
Martin, AM ;
Jimenez-Sainz, MC ;
Martinez-A, C ;
Mayor, F .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (06) :2985-2990
[9]   Dissociation of chemotaxis from agonist-induced receptor internalization in a lymphocyte cell line transfected with CCR2B - Evidence that directed migration does not require rapid modulation of signaling at the receptor level [J].
Arai, H ;
Monteclaro, FS ;
Tsou, CL ;
Franci, C ;
Charo, IF .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (40) :25037-25042
[10]   Molecular mechanism of desensitization of the chemokine receptor CCR-5: receptor signaling and internalization are dissociable from its role as an HIV-1 co-receptor [J].
Aramori, I ;
Zhang, J ;
Ferguson, SSG ;
Bieniasz, PD ;
Cullen, BR ;
Caron, MG .
EMBO JOURNAL, 1997, 16 (15) :4606-4616