Src and Syk kinases:: key regulators of phagocytic cell activation

被引:186
作者
Berton, G
Mócsai, A
Lowell, CA
机构
[1] Univ Verona, Dept Pathol, Sect Gen Pathol, I-37134 Verona, Italy
[2] Semmelweis Univ, Sch Med, Dept Physiol, H-1444 Budapest, Hungary
[3] Univ Calif San Francisco, Dept Lab Med, San Francisco, CA 94143 USA
关键词
D O I
10.1016/j.it.2005.02.002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Src-family kinases and Syk tyrosine kinases have crucial roles in multiple leukocyte intracellular signaling pathways. In immunoreceptor-related pathways, these enzymes work together sequentially, with Src-family kinases phosphorylating specific protein substrates, which in turn recruit and activate Syk. Recent evidence indicates that several non-immunoreceptors also use Src-family kinases and Syk in this same fashion. In leukocyte integrin signaling, the interaction between the kinases is more complex, where they appear to act in a sequential manner but the mechanisms by which they are activated remain poorly defined. Elucidating the regulation of these tyrosine kinase-based signaling pathways in leukocytes remains an important goal in understanding how immune cells respond to the multitude of activating agents they encounter.
引用
收藏
页码:208 / 214
页数:7
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