Is the CD200/CD200 receptor interaction more than just a myeloid cell lnhibitory signal?

被引:86
作者
Minas, Konstantinos [1 ]
Liversidge, Janet [1 ]
机构
[1] Univ Aberdeen, Inst Med Sci, Dept Ophthalmol, Aberdeen AB25 2ZD, Scotland
基金
英国惠康基金;
关键词
monocyte-macrophage; dendritic cells; autoimmunity; allergy; transplantation;
D O I
10.1615/CritRevImmunol.v26.i3.20
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The membrane glycoprotein CD200, which has a widespread but defined distribution and a structurally similar receptor (CD200R) that transmits an inhibitory signal to cells of the hematopoetic lineage, especially myeloid cells, has been characterized. CD20OR expression is restricted predominantly to cells of the myeloid lineage indicating that this ligand/receptor pair has a specific role in controlling myeloid cell function. In addition to CD200R, several related genes have been identified. Whether these gene products also regulate immune function is controversial. CD20OR is also expressed by certain subsets of T cells and CD200 may be expressed by antigen-presenting cells, adding additional layers of complexity to the CD200/CD200R axis. Because monocytic myeloid cells provide a link between the innate and adaptive immune response, mechanisms to control their function through receptors such as CD20OR will have therapeutic potential. Regulation of immune responses is accomplished by the concerted, but opposing, activity of kinases and phosphatases, fine control often being achieved through paired receptors. In this review, we will consider whether CD20OR signaling functions within a framework of paired activating and inhibitory receptors and whether the inhibitory signal delivered has functional consequences beyond inhibition of myeloid cell proinflammatory activation.
引用
收藏
页码:213 / 230
页数:18
相关论文
共 130 条
[1]   Mechanisms of central and peripehral T-cell tolerance: lessons from experimental models of multiple sclerosis [J].
Anderton, S ;
Burkhart, C ;
Metzler, B ;
Wraith, D .
IMMUNOLOGICAL REVIEWS, 1999, 169 :123-137
[2]   Direct recognition of cytomegalovirus by activating and inhibitory NK cell receptors [J].
Arase, H ;
Mocarski, ES ;
Campbell, AE ;
Hill, AB ;
Lanier, LL .
SCIENCE, 2002, 296 (5571) :1323-1326
[3]   DAP12-deficient mice fail to develop autoimmunity due to impaired antigen priming [J].
Bakker, ABH ;
Hoek, RM ;
Cerwenka, A ;
Blom, B ;
Lucian, L ;
McNeil, T ;
Murray, R ;
Phillips, JH ;
Sedgwick, JD ;
Lanier, LL .
IMMUNITY, 2000, 13 (03) :345-353
[4]   Blocking CD200-CD200 receptor axis augments NOS-2 expression and aggravates experimental autoimmune uveoretinitis in Lewis rats [J].
Banerjee, D ;
Dick, AD .
OCULAR IMMUNOLOGY AND INFLAMMATION, 2004, 12 (02) :115-125
[5]   Membrane proteins with immunoglobulin-like domains - a master superfamily of interaction molecules [J].
Barclay, AN .
SEMINARS IN IMMUNOLOGY, 2003, 15 (04) :215-223
[6]   CD200 and membrane protein E interactions in the control of myeloid cells [J].
Barclay, AN ;
Wright, GJ ;
Brooke, G ;
Brown, MH .
TRENDS IN IMMUNOLOGY, 2002, 23 (06) :285-290
[7]   PURIFICATION AND CHEMICAL CHARACTERIZATION OF MEMBRANE-GLYCOPROTEINS FROM RAT THYMOCYTES AND BRAIN, RECOGNIZED BY MONOCLONAL-ANTIBODY MRC-OX2 [J].
BARCLAY, AN ;
WARD, HA .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1982, 129 (02) :447-458
[8]  
BARCLAY AN, 2005, LEUKOCYTE ANTIGENS F
[9]   Studying the immunosuppressive role of indoleamine 2,3-dioxygenase:: tryptophan metabolites suppress rat allogeneic T-cell responses in vitro and in vivo [J].
Bauer, TM ;
Jiga, LP ;
Chuang, JJ ;
Randazzo, M ;
Opelz, G ;
Terness, P .
TRANSPLANT INTERNATIONAL, 2005, 18 (01) :95-100
[10]   The paired Ig-like receptor PIR-B is an inhibitory receptor that recruits the protein-tyrosine phosphatase SHP-1 [J].
Bléry, M ;
Kubagawa, H ;
Chen, CC ;
Vély, F ;
Cooper, MD ;
Vivier, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (05) :2446-2451