The Syk family of protein tyrosine kinases in T-cell activation and development
The processes of T‐cell development and activation employ similar immature and mature receptors as well as similar signal transduction pathways to achieve different outcomes. Many signaling molecules are shared between [he receptor signaling pathways, including two families of cytoplasmic protein ty...
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Published in | Immunological reviews Vol. 165; no. 1; pp. 167 - 180 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Oxford, UK
Blackwell Publishing Ltd
01.10.1998
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Subjects | |
Online Access | Get full text |
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Summary: | The processes of T‐cell development and activation employ similar immature and mature receptors as well as similar signal transduction pathways to achieve different outcomes. Many signaling molecules are shared between [he receptor signaling pathways, including two families of cytoplasmic protein tyrosine kinases, the Src family and the Syk family. The two Syk family members expressed in T cells, Syk and ZAP‐70, are structurally similar but are expressed at different times during rhymic development and during T‐cell activation. These two kinases, althongh they share many physical features, differ in terms of biochemical activity and regulation. We discuss the overlapping and distinct characteristics of Syk and ZAP‐70 in T‐cell signaling and the potential biological importance of their differences. |
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Bibliography: | ArticleID:IMR167 ark:/67375/WNG-58DCG2B7-7 istex:276C8BE5E1216CE3C5E2D5701F23AE80A6938DC2 Acknowledgements The authors would like to thank Drs, Robert Abraham and Oreste Acuto for sharing unpublished data, as well as Drs, Lawrence Kane, Deborah Yelon, and Qihong Zhao for critical reading of the manuscript. This research is supported by the Medical Scientist Training Program, American College of Rheumatology, Arthritis Foundation, Howard Hughes Medical Institute, HHMI Research Resources Program, and National Institutes of Health. ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-3 content type line 23 ObjectType-Review-1 |
ISSN: | 0105-2896 1600-065X |
DOI: | 10.1111/j.1600-065X.1998.tb01238.x |