TARGETED DISRUPTION OF THE P50 SUBUNIT OF NF-KAPPA-B LEADS TO MULTIFOCAL DEFECTS IN IMMUNE-RESPONSES

被引:1034
作者
SHA, WC
LIOU, HC
TUOMANEN, EI
BALTIMORE, D
机构
[1] MIT,DEPT BIOL,CAMBRIDGE,MA 02139
[2] CORNELL UNIV,COLL MED,DEPT CELL BIOL,DIV ALLERGY & IMMUNOL,NEW YORK,NY 10021
[3] CORNELL UNIV,COLL MED,DEPT MED,DIV ALLERGY & IMMUNOL,NEW YORK,NY 10021
[4] ROCKEFELLER UNIV,MOLEC INFECT DIS LAB,NEW YORK,NY 10021
关键词
D O I
10.1016/0092-8674(95)90415-8
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
NF-kappa B, a heterodimeric transcription factor composed of p50 and p65 subunits, can be activated in many cell types and is thought to regulate a wide variety of genes involved in immune function and development, Mice lacking the p50 subunit of NF-kappa B show no developmental abnormalities, but exhibit multifocal defects in immune responses involving B lymphocytes and nonspecific responses to infection. B cells do not proliferate in response to bacterial lipopolysaccharide and are defective in basal and specific antibody production. Mice lacking p50 are unable effectively to clear L. monocytogenes and are more susceptible to infection with S. pneumoniae, but are more resistant to infection with murine encephalomyocarditis virus. These data support the role of NF-kappa B as a vital transcription factor for both specific and nonspecific immune responses, but do not indicate a developmental role for the factor.
引用
收藏
页码:321 / 330
页数:10
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