Loss of p27Kip1 enhances the transplantation efficiency of hepatocytes transferred into diseased livers

被引:42
作者
Karnezis, AN
Dorokhov, M
Grompe, M
Zhu, L
机构
[1] Albert Einstein Coll Med, Dept Dev & Mol Biol, Bronx, NY 10461 USA
[2] Albert Einstein Coll Med, Dept Med, Bronx, NY 10461 USA
[3] Albert Einstein Coll Med, Marion Bessin Liver Res Ctr, Bronx, NY 10461 USA
[4] Oregon Hlth Sci Univ, Dept Pediat, Portland, OR 97201 USA
[5] Oregon Hlth Sci Univ, Dept Mol & Med Genet, Portland, OR 97201 USA
关键词
D O I
10.1172/JCI200111933
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
p27(Kip1) is an important regulator of cyclin-dependent kinases. Studies with p27 knockout mice have revealed abnormalities in proliferation and differentiation of multiple cell types. Here we show that primary hepatocytes isolated from livers of adult p27 knockout mice exhibit higher levels of DNA synthesis activity in culture than do wild-type cells. Interestingly, we found that, compared with control hepatocytes, p27 knockout hepatocytes proliferate better after transplantation into diseased livers to reverse liver failure. These results reveal an aspect of p27 that could be used to benefit cell-based therapy.
引用
收藏
页码:383 / 390
页数:8
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