Targeted disruption of the mouse Stat3 gene leads to early embryonic lethality

被引:1090
作者
Takeda, K
Noguchi, K
Shi, W
Tanaka, T
Matsumoto, M
Yoshida, N
Kishimoto, T
Akira, S
机构
[1] HYOGO MED UNIV,DEPT BIOCHEM,NISHINOMIYA,HYOGO 663,JAPAN
[2] HYOGO MED UNIV,DEPT ANAT & NEUROSCI,NISHINOMIYA,HYOGO 663,JAPAN
[3] OSAKA UNIV,SCH MED,DEPT MED 3,SUITA,OSAKA 565,JAPAN
[4] OSAKA MED CTR MATERNAL & CHILD HLTH,RES INST,ISUMI,OSAKA 59002,JAPAN
关键词
D O I
10.1073/pnas.94.8.3801
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
Signal transducer and activator of transcription (STAT) proteins have been shown to mediate biological actions in response to cytokines. Stat3, a member of the STAT family, is activated by a variety of cytokines, including the interleukin 6 family of cytokines, leptin, granulocyte colony-stimulating factor, and epidermal growth factor. To address the biological function of Stat3, we generated mice deficient in Stat3 by gene targeting. No viable Stat3-deficient mice could be obtained from heterozygote intercross. Analysis of embryos at several gestation times revealed that Stat3-deficient embryos showed a rapid degeneration between embryonic days 6.5 and 7.5, although they developed into the egg cylinder stage until embryonic day 6.0. These results demonstrate that Stat3 is essential for the early development of mouse embryos.
引用
收藏
页码:3801 / 3804
页数:4
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