The Interaction Between Signal Regulatory Protein Alpha (SIRPα) and CD47: Structure, Function, and Therapeutic Target

被引:614
作者
Barclay, A. Neil [1 ]
van den Berg, Timo K. [2 ]
机构
[1] Univ Oxford, Sir William Dunn Sch Pathol, Oxford OX1 3RE, England
[2] Univ Amsterdam, Acad Med Ctr, Sanquin Res & Landsteiner Lab, NL-1066 CX Amsterdam, Netherlands
来源
ANNUAL REVIEW OF IMMUNOLOGY, VOL 32 | 2014年 / 32卷
基金
英国医学研究理事会;
关键词
paired receptor; CD47; SIRP alpha; phagocytosis; cancer; inflammation; TYROSINE-PHOSPHATASE SUBSTRATE-1; AUTOIMMUNE HEMOLYTIC-ANEMIA; INTEGRIN-ASSOCIATED PROTEIN; HEMATOPOIETIC STEM-CELLS; COLLAGEN-INDUCED ARTHRITIS; INNATE IMMUNE ACTIVATION; NON-HODGKIN-LYMPHOMA; RED-BLOOD-CELLS; HUMAN T-CELL; DENDRITIC CELLS;
D O I
10.1146/annurev-immunol-032713-120142
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
CD47 is a broadly expressed membrane protein that interacts with the myeloid inhibitory immunoreceptor SIRP alpha (also termed CD172a or SHPS-1). SIRP alpha is the prototypic member of the SIRP paired receptor family of closely related SIRP proteins. Engagement of SIRP alpha by CD47 provides a downregulatory signal that inhibits host cell phagocytosis, and CD47 therefore functions as a "don't-eat-me" signal. Here, we discuss recent structural analysis of CD47-SIRP alpha interactions and implications of this for the function and evolution of SIRP alpha and paired receptors in general. Furthermore, we review the proposed roles of CD47-SIRP alpha interactions in phagocytosis, (auto) immunity, and host defense, as well as its potential significance as a therapeutic target in cancer and inflammation and for improving graft survival in xenotransplantation.
引用
收藏
页码:25 / 50
页数:26
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