An essential role for BLNK in human B cell development

被引:251
作者
Minegishi, Y
Rohrer, J
Coustan-Smith, E
Lederman, HM
Pappu, R
Campana, D
Chan, AC
Conley, ME
机构
[1] St Jude Childrens Res Hosp, Dept Immunol, Memphis, TN 38105 USA
[2] Johns Hopkins Hosp, Dept Pediat, Div Pediat Allergy & Immunol, Baltimore, MD 21287 USA
[3] Washington Univ, Sch Med, Howard Hughes Med Inst, Dept Med,Div Rheumatol,Ctr Immunol, St Louis, MO 63110 USA
[4] Washington Univ, Sch Med, Howard Hughes Med Inst, Dept Pathol, St Louis, MO 63110 USA
[5] Univ Tennessee, Coll Med, Dept Pediat, Memphis, TN 38105 USA
关键词
D O I
10.1126/science.286.5446.1954
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The signal transduction events that control the progenitor B cell (pro-B cell) to precursor B cell (pre-B cell) transition have not been well delineated. In evaluating patients with absent B cells, a male with a homozygous splice defect in the cytoplasmic adapter protein BLNK (B cell Linker protein) was identified. Although this patient had normal numbers of pro-B cells, he had no pre-B cells or mature B cells, indicating that BLNK plays a critical role in orchestrating the pro-B cell to pre-B cell transition. The immune system and overall growth and development were otherwise normal in this patient, suggesting that BLNK function is highly specific.
引用
收藏
页码:1954 / 1957
页数:4
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