Signalling of Bruton's tyrosine kinase, Btk

被引:1
|
作者
Mohamed, AJ
Nore, BF
Christensson, B
Smith, CIE [1 ]
机构
[1] Huddinge Hosp, Karolinska Inst, Dept Clin Immunol Microbiol Pathol & Infect Dis, S-14186 Huddinge, Sweden
[2] Karolinska Inst, Novum, Ctr Biotechnol, S-14104 Huddinge, Sweden
[3] Karolinska Inst, Novum, Dept Biosci, S-14104 Huddinge, Sweden
[4] Univ Coll S Stockholm, S-14104 Huddinge, Sweden
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D O I
暂无
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Bruton's tyrosine kinase, which is encoded by the BTK gene, is a cytoplasmic protein tyrosine kinase (PTK) crucial for B-cell development and differentiation. It belongs to the Tec family of PTKs containing several domains that are characteristic of signalling molecules. In humans, mutations that disrupt the function of this gene lead to the classical XLA syndrome (X-linked agammaglobulinaemia), a primary immunodeficiency mainly characterized by lack of mature B cells as well as low levels of immunoglobulins. In contrast, animal models of this disease such as the xid mice display profoundly milder XLA phenotype. BTK phosphorylation and activation in response to engagement of the B-cell receptor (BCR) by antigen is a dynamic process whereby a variety of proteins interact with each other and recruit signalling molecules resulting in a physiological response such as B-cell proliferation and antibody production. The main players, however, that participate in the intracellular downstream cascade have not yet been identified and are therefore under intense scrutiny in several laboratories. This review discusses certain aspects of BTK activation following receptor stimulation by agonists and how this event is translated into the biochemical signals within the cell that eventually lead to nuclear responses.
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页码:113 / 118
页数:6
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