Differential cyclin D1 requirements of proliferating Schwann cells during development and after injury

被引:55
作者
Atanasoski, S
Shumas, S
Dickson, C
Scherer, SS
Suter, U [1 ]
机构
[1] ETH Honggerberg, Inst Cell Biol, Dept Biol, Swiss Fed Inst Technol, CH-8093 Zurich, Switzerland
[2] Univ Penn, Dept Neurol, Sch Med, Philadelphia, PA 19104 USA
[3] Imperial Canc Res Fund, Viral Carcinogenesis Lab, London WC2A 3PX, England
基金
美国国家卫生研究院;
关键词
D O I
10.1006/mcne.2001.1055
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Neurons regulate Schwann cell proliferation, but little is known about the molecular basis of this interaction. We have examined the possibility that cyclin D1 is a key regulator of the cell cycle in Schwann cells. Myelinating Schwann cells express cyclin D1 in the perinuclear region, but after axons are severed, cyclin D1 is strongly upregulated in parallel with Schwann cell proliferation and translocates into Schwann cell nuclei. During development, cyclin D1 expression is confined to the perinuclear region of proliferating Schwann cells and the analysis of cyclin D1-null mice indicates that cyclin D1 is not required for this type of Schwann cell proliferation. As in the adult, injury to immature peripheral nerves leads to translocation of cyclin D1 to Schwann cell nuclei and injury-induced proliferation is impaired in both immature and mature cyclin D1 -deficient Schwann cells. Thus, our data indicate that the molecular mechanisms regulating proliferation of Schwann cells during development or activated by axonal damage are fundamentally different.
引用
收藏
页码:581 / 592
页数:12
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