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The Interaction Between Signal Regulatory Protein Alpha (SIRPα) and CD47: Structure, Function, and Therapeutic Target
被引:551
|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:
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.
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页码:25 / 50
页数:26
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