Myelinating Schwann cells determine the internodal localization of Kv1.1, Kv1.2, Kvβ2, and Caspr

被引:89
作者
Arroyo, EJ
Xu, YT
Zhou, L
Messing, A
Peles, E
Chiu, SY
Scherer, SS [1 ]
机构
[1] Univ Penn, Med Ctr, Dept Neurol, Philadelphia, PA 19104 USA
[2] Univ Wisconsin, Dept Physiol, Madison, WI 53706 USA
[3] Univ Wisconsin, Sch Vet Med, Dept Pathobiol Sci, Madison, WI 53706 USA
[4] Weizmann Inst Sci, Dept Mol Cell Biol, IL-76100 Rehovot, Israel
来源
JOURNAL OF NEUROCYTOLOGY | 1999年 / 28卷 / 4-5期
关键词
D O I
10.1023/A:1007009613484
中图分类号
Q2 [细胞生物学];
学科分类号
071009 [细胞生物学]; 090102 [作物遗传育种];
摘要
We examined the localization of Caspr and the K+ channels Kv1.1 and Kv1.2, all of which are intrinsic membrane proteins of myelinated axons in the PNS. Caspr is localized to the paranode; Kv1.1, Kv1.2 and their beta 2 subunit are localized to the juxtaparanode. Throughout the internodal region, a strand of Caspr staining is flanked by a double strand of Kv1.1/Kv1.2/Kv beta 2 staining. This tripartite strand apposes the inner mesaxon of the myelin sheath, and forms a circumferential ring that apposes the innermost aspect of Schmidt-Lanterman incisures. The localization of Caspr and Kv1.2 are not disrupted in mice with null mutations of the myelin associated glycoprotein, connexin32, or Kv1.1 genes. At all of these locations, Caspr and Kv1.1/Kv1.2/Kv beta 2 define distinct but interrelated domains of the axonal membrane that appear to be organized by the myelin sheath.
引用
收藏
页码:333 / 347
页数:15
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