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.
Skip Nav Destination
Article navigation
6 September 1999
Article|
September 06 1999
Heterophilic Binding of L1 on Unmyelinated Sensory Axons Mediates Schwann Cell Adhesion and Is Required for Axonal Survival
C.A. Haney,
C.A. Haney
aDepartment of Neuroscience, School of Medicine, Case Western Reserve University, Cleveland, Ohio 44106
bDepartment of Neurosciences, Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, Ohio 44195
Search for other works by this author on:
Z. Sahenk,
Z. Sahenk
cDepartment of Neurology, Neuromuscular Disease Center, College of Medicine, Ohio State University, Columbus, Ohio 43210
Search for other works by this author on:
C. Li,
C. Li
dSamuel Lunenfeld Research Institute, Mt. Sinai Hospital, Department of Molecular and Medical Genetics, University of Toronto, Toronto, Canada
Search for other works by this author on:
V.P. Lemmon,
V.P. Lemmon
aDepartment of Neuroscience, School of Medicine, Case Western Reserve University, Cleveland, Ohio 44106
Search for other works by this author on:
J. Roder,
J. Roder
dSamuel Lunenfeld Research Institute, Mt. Sinai Hospital, Department of Molecular and Medical Genetics, University of Toronto, Toronto, Canada
Search for other works by this author on:
B.D. Trapp
B.D. Trapp
aDepartment of Neuroscience, School of Medicine, Case Western Reserve University, Cleveland, Ohio 44106
bDepartment of Neurosciences, Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, Ohio 44195
Search for other works by this author on:
C.A. Haney
aDepartment of Neuroscience, School of Medicine, Case Western Reserve University, Cleveland, Ohio 44106
bDepartment of Neurosciences, Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, Ohio 44195
Z. Sahenk
cDepartment of Neurology, Neuromuscular Disease Center, College of Medicine, Ohio State University, Columbus, Ohio 43210
C. Li
dSamuel Lunenfeld Research Institute, Mt. Sinai Hospital, Department of Molecular and Medical Genetics, University of Toronto, Toronto, Canada
V.P. Lemmon
aDepartment of Neuroscience, School of Medicine, Case Western Reserve University, Cleveland, Ohio 44106
J. Roder
dSamuel Lunenfeld Research Institute, Mt. Sinai Hospital, Department of Molecular and Medical Genetics, University of Toronto, Toronto, Canada
B.D. Trapp
aDepartment of Neuroscience, School of Medicine, Case Western Reserve University, Cleveland, Ohio 44106
bDepartment of Neurosciences, Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, Ohio 44195
1.used in this paper: CST, cervical sympathetic trunk; DRG, dorsal root ganglia; L4, lumbar dorsal root 4; L5, lumbar dorsal root 5; MAG, myelin-associated glycoprotein; PNS, peripheral nervous system; SCG, superior sympathetic ganglia
Received:
June 08 1999
Revision Requested:
July 23 1999
Accepted:
July 23 1999
Online ISSN: 1540-8140
Print ISSN: 0021-9525
© 1999 The Rockefeller University Press
1999
The Rockefeller University Press
J Cell Biol (1999) 146 (5): 1173–1184.
Article history
Received:
June 08 1999
Revision Requested:
July 23 1999
Accepted:
July 23 1999
Citation
C.A. Haney, Z. Sahenk, C. Li, V.P. Lemmon, J. Roder, B.D. Trapp; Heterophilic Binding of L1 on Unmyelinated Sensory Axons Mediates Schwann Cell Adhesion and Is Required for Axonal Survival. J Cell Biol 6 September 1999; 146 (5): 1173–1184. doi: https://doi.org/10.1083/jcb.146.5.1173
Download citation file:
Sign in
Don't already have an account? Register
Client Account
You could not be signed in. Please check your email address / username and password and try again.
Could not validate captcha. Please try again.
Sign in via your Institution
Sign in via your InstitutionSuggested Content
Email alerts
Advertisement
Advertisement