DNA degradation in development and programmed cell death

被引:177
作者
Nagata, S [1 ]
机构
[1] Osaka Univ, Genet Lab, Lab Integrated Biol, Grad Sch Frontier Biosci, Osaka, Japan
[2] Osaka Univ, Sch Med, Dept Genet, Osaka, Japan
[3] Japanese Sci & Technol Agcy, Solut Oriented Res Sci & Technol, Osaka, Japan
关键词
apoptosis; erythropoiesis; lens cell differentiation; tissue atrophy; anemia; cataract; autoimmune disease;
D O I
10.1146/annurev.immunol.23.021704.115811
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Most mammalian cells have nuclei that contain DNA, which replicates during cell proliferation. DNA is destroyed by various developmental processes in mammals. It is degraded during programmed cell death that accompanies mammalian development. The nuclei of erythrocytes and eye lens fiber cells are also removed during their differentiation into mature cells. If DNA is not properly degraded in these processes, it can cause various diseases, including tissue atrophy, anemia, cataract, and autoimmune diseases, which indicates that DNA can be a pathogenic molecule. Here, I present how DNA is degraded during programmed cell death, erythroid cell differentiation, and lens cell differentiation. I discuss what might be or will be learned from understanding the molecular mechanisms of DNA degradation that occurs during mammalian development.
引用
收藏
页码:853 / 875
页数:23
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