EXPRESSION OF SURROGATE LIGHT CHAIN RECEPTORS IS RESTRICTED TO A LATE STAGE IN PRE-B CELL-DIFFERENTIATION

被引:151
作者
LASSOUED, K
NUNEZ, CA
BILLIPS, L
KUBAGAWA, H
MONTEIRO, RC
LEBIEN, TW
COOPER, MD
机构
[1] UNIV ALABAMA, DEPT PEDIAT, DIV DEV & CLIN IMMUNOL, BIRMINGHAM, AL 35294 USA
[2] UNIV ALABAMA, DEPT PATHOL, DIV DEV & CLIN IMMUNOL, BIRMINGHAM, AL 35294 USA
[3] UNIV ALABAMA, DEPT MICROBIOL, DIV DEV & CLIN IMMUNOL, BIRMINGHAM, AL 35294 USA
[4] UNIV ALABAMA, HOWARD HUGHES MED INST, BIRMINGHAM, AL 35294 USA
[5] UNIV MINNESOTA, SCH MED, DEPT LAB MED & PATHOL, MINNEAPOLIS, MN 55455 USA
关键词
D O I
10.1016/0092-8674(93)90161-I
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Surrogate light chain (psiLC) genes are transcriptionally active in progenitor B (pro-B) cells before immunoglobulin genes are rearranged. Current hypothetical models suggest that the psiLC proteins may couple with surrogate or conventional heavy chain proteins to form cell surface receptors that signal the progressive differentiation of pro-B, precursor B (pre-B), and immature B cells. Monoclonal antibodies were produced and used to examine the synthesis, expression, intermolecular interaction, and function of psiLC during B cell differentiation. The results indicate that, while psiLC production spans several developmental stages, cell surface expression is confined to a relatively late stage in normal pre-B cell differentiation, during which receptor cross-linkage does not impede cell growth or B cell differentiation.
引用
收藏
页码:73 / 86
页数:14
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