Heterophilic binding of L1 on unmyelinated sensory axons mediates schwann cell adhesion and is required for axonal survival

被引:103
作者
Haney, CA
Sahenk, Z
Li, C
Lemmon, VP
Roder, J
Trapp, BD
机构
[1] Cleveland Clin Fdn, Lerner Res Inst, Dept Neurosci, Cleveland, OH 44195 USA
[2] Case Western Reserve Univ, Sch Med, Dept Neurosci, Cleveland, OH 44106 USA
[3] Ohio State Univ, Coll Med, Dept Neurol, Neuromuscular Dis Ctr, Columbus, OH 43210 USA
[4] Univ Toronto, Mt Sinai Hosp, Dept Mol & Med Genet, Samuel Lunenfeld Res Inst, Toronto, ON M5G 1X5, Canada
关键词
cell adhesion; cell polarity; axonal degeneration; L1; myelin-associated glycoprotein;
D O I
10.1083/jcb.146.5.1173
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
This study investigated the function of the adhesion molecule L1 in unmyelinated fibers of the peripheral nervous system (PNS) by analysis of L1-deficient mice. We demonstrate that L1 is present on axons and Schwann cells of sensory unmyelinated fibers, but only on Schwann cells of sympathetic unmyelinated fibers. In L1-deficient sensory nerves, Schwann cells formed but failed to retain normal axonal ensheathment. L1-deficient mice had reduced sensory function and loss of unmyelinated axons, while sympathetic unmyelinated axons appeared normal. In nerve transplant studies, loss of axonal-L1, but not Schwann cell-L1, reproduced the L1-deficient phenotype. These data establish that heterophilic axonal-L1 interactions mediate adhesion between unmyelinated sensory axons and Schwann cells, stabilize the polarization of Schwann cell surface membranes, and mediate a trophic effect that assures axonal survival.
引用
收藏
页码:1173 / 1183
页数:11
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