Immunosenescence phenotypes in the telomerase knockout mouse

被引:37
作者
Blasco, MA [1 ]
机构
[1] CSIC, Ctr Nacl Biotecnol, Dept Immunol & Oncol, E-28049 Madrid, Spain
来源
SPRINGER SEMINARS IN IMMUNOPATHOLOGY | 2002年 / 24卷 / 01期
关键词
D O I
10.1007/s00281-001-0096-1
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Increasing generations of the telomerase knockout mouse, Terc(-/-), show severe telomere dysfunction characterized by critically short telomeres and end-to-end chromosomal fusions. These mice also suffer from various age-related diseases affecting highly proliferative tissues. Among these pathologies are a reduced proliferative capacity of B and T cells, as well as a reduction of germinal center reactivity upon immunization. Both immune system defects are landmarks of immunosenescence. The study of the telomerase-deficient mouse model supports the notion that telomere shortening with age contributes to immunological dysfunction in the elderly.
引用
收藏
页码:75 / 85
页数:11
相关论文
共 73 条
[71]   Immunosenescence and germinal center reaction [J].
Zheng, B ;
Han, SH ;
Takahashi, Y ;
Kelsoe, G .
IMMUNOLOGICAL REVIEWS, 1997, 160 :63-77
[72]   Cell-cycle-regulated association of RAD50/MRE11/NBS1 with TRF2 and human telomeres [J].
Zhu, XD ;
Küster, B ;
Mann, M ;
Petrini, JHJ ;
de Lange, T .
NATURE GENETICS, 2000, 25 (03) :347-352
[73]   Telomeres: has cancer's Achilles' heel been exposed? [J].
Zumstein, LA ;
Lundblad, V .
NATURE MEDICINE, 1999, 5 (10) :1129-1130