A developmentally regulated switch directs regenerative growth of Schwann cells through cyclin D1

被引:80
作者
Kim, HA
Pomeroy, SL
Whoriskey, W
Pawlitzky, I
Benowitz, LI
Sicinski, P
Stiles, CD [1 ]
Roberts, TM
机构
[1] Childrens Hosp, Dana Farber Canc Inst, Dept Canc Biol, Boston, MA 02115 USA
[2] Childrens Hosp, Dept Neurol, Boston, MA 02115 USA
[3] Childrens Hosp, Dept Neurosurg, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Boston, MA 02115 USA
关键词
D O I
10.1016/S0896-6273(00)81173-3
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Sciatic nerve axons in cyclin D1 knockout mice develop normally, become properly ensheathed by Schwann cells, and appear to function normally. However, in the Wallerian degeneration model of nerve injury, the mitotic response of Schwann cells is completely inhibited. The mitotic block is Schwann cell autonomous and developmentally regulated. Rescue analysis (by "knockin" of cyclin E) indicates that D1 protein, rather than regulatory elements of the D1 gene, provides the essential Schwann cell function. Genetic inhibition of the Schwann cell cycle shows that neuronal responses to nerve injury are surprisingly independent of Schwann cell mitotic responses. Even axonal regrowth into the distal zone of a nerve crush injury is not markedly impaired in cyclin D1(-/-) mice.
引用
收藏
页码:405 / 416
页数:12
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