TARGETED DISRUPTION OF THE MOUSE TRANSFORMING GROWTH FACTOR-BETA-1 GENE RESULTS IN MULTIFOCAL INFLAMMATORY DISEASE

被引:2645
作者
SHULL, MM [1 ]
ORMSBY, I [1 ]
KIER, AB [1 ]
PAWLOWSKI, S [1 ]
DIEBOLD, RJ [1 ]
YIN, MY [1 ]
ALLEN, R [1 ]
SIDMAN, C [1 ]
PROETZEL, G [1 ]
CALVIN, D [1 ]
ANNUNZIATA, N [1 ]
DOETSCHMAN, T [1 ]
机构
[1] UNIV CINCINNATI, COLL MED, DEPT PATHOL & LAB MED, DIV COMPARAT PATHOL, CINCINNATI, OH 45267 USA
关键词
D O I
10.1038/359693a0
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 [理学]; 0710 [生物学]; 09 [农学];
摘要
Transforming growth factor-beta1 (TGF-beta1) is a multifunctional growth factor that has profound regulatory effects on many developmental and physiological processes. Disruption of the TGF-beta1 gene by homologous recombination in murine embryonic stem cells enables mice to be generated that carry the disrupted allele. Animals homozygous for the mutated TGF-beta1 allele show no gross developmental abnormalities, but about 20 days after birth they succumb to a wasting syndrome accompanied by a multifocal, mixed inflammatory cell response and tissue necrosis, leading to organ failure and death. TGF-beta1-deficient mice may be valuable models for human immune and inflammatory disorders, including autoimmune diseases, transplant rejection and graft versus host reactions.
引用
收藏
页码:693 / 699
页数:7
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