EXPRESSION OF BRUTONS TYROSINE KINASE PROTEIN WITHIN THE B-CELL LINEAGE

被引:93
作者
GENEVIER, HC
HINSHELWOOD, S
GASPAR, HB
RIGLEY, KP
BROWN, D
SAELAND, S
ROUSSET, F
LEVINSKY, RJ
CALLARD, RE
KINNON, C
LOVERING, RC
机构
[1] INST CHILD HLTH,MOLEC IMMUNOL UNIT,LONDON WC1N 1EH,ENGLAND
[2] INST CHILD HLTH,CELLULAR IMMUNOL UNIT,LONDON WC1N 1EH,ENGLAND
[3] SCHERING PLOUGH CORP,CTR RECH,DARDILLY,FRANCE
[4] CELLTECH LTD,SLOUGH SL1 4EN,BERKS,ENGLAND
基金
英国惠康基金;
关键词
B CELLS; BRUTONS TYROSINE KINASE; IMMUNODEFICIENCY; TYROSINE KINASE; X-LINKED AGAMMAGLOBULINEMIA;
D O I
10.1002/eji.1830241228
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Defects in the gene encoding Bruton's tyrosine kinase (Btk), normally expressed in B cells, cause X-linked agammaglobulinemia (XLA). The phenotype of XLA is characterized by a lack of circulating B cells and immunoglobulin. It has been suggested that B cell maturation from the pre-B cell stage to more mature stages is dependent on the appropriate expression of this gene. The Btk mRNA is expressed in B cells and myeloid cells, but protein expression in relation to B cell maturation has not been determined. Moreover, expression of the Btk protein has so far only been investigated in human Epstein-Barr virus-transformed B cell lines, and in murine splenocytes and B cell lines. We have developed an antiserum which recognizes the human Btk protein and shown that normal human tonsillar B cells, peripheral blood monocytes and myeloid cells express the protein, whereas tonsil-derived T cells do not. We also show that the protein is present in early and mature human B cell lines, but is absent in terminally differentiated plasma cell lines. Furthermore, expression is reduced or absent in three B lineage cell lines derived from two patients with defined genetic mutations in Btk and suffering from XLA.
引用
收藏
页码:3100 / 3105
页数:6
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