Tonic B-cell and viral ITAM signaling: Context is everything

被引:15
作者
Grande, Shannon M.
Bannish, Gregory
Fuentes-Panana, Ezequiel M.
Katz, Elad
Monroe, John G.
机构
[1] Univ Penn, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
[2] Univ Penn, Abramson Family Canc Res Inst, Philadelphia, PA 19104 USA
[3] UIMEIP, Hosp Pediatria, Mexico City, DF, Mexico
[4] Western Gen Hosp, Canc Res Ctr, Edinburgh EH4 2XU, Midlothian, Scotland
关键词
lymphopoiesis; signal transduction; antigen receptors; neoplastic cell transformation; immunoreceptors;
D O I
10.1111/j.1600-065X.2007.00535.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
The presence of an immunoreceptor tyrosine-based activation motif (ITAM) makes immunoreceptors different from other signaling receptors, like integrins, G-coupled protein receptors, chemokine receptors, and growth factor receptors. This unique motif has the canonical sequence D/Ex(0-2)YxxL/Ix(6-8)YxxL/I, where x represents any amino acid and is present at least once in all immunoreceptor complexes. Immunoreceptors can promote survival, activation, and differentiation by transducing signals through these highly conserved motifs. Traditionally, ITAM signaling is thought to occur in response to ligand-induced aggregation, although evidence indicates that ligand-independent tonic signaling also provides functionally relevant signals. The majority of proteins containing ITAMs are transmembrane proteins that exist as part of immunoreceptor complexes. However, oncogenic viruses also have ITAM-containing proteins. In this review, we discuss what is known about tonic signaling by both cellular and viral ITAM-containing proteins and speculate what we might learn from each context.
引用
收藏
页码:214 / 234
页数:21
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