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PMID: 2333149 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Large diameter primary afferent input is required for expression of the Cat-301 proteoglycan on the surface of motor neurons.

Neuroscience ·Vol. 34 ·No. 2 ·1990-00-00 ·Pages 391-401

Kalb RG, Hockfield S

Abstract

The expression of a cell surface proteoglycan, recognized by monoclonal antibody Cat-301, is regulated by neuronal activity in early life. Here we report that the expression of the Cat-301 proteoglycan on motor neurons depends on primary afferent input in the early postnatal period. Previously we showed that in two different systems, Y-cells in the cat lateral geniculate nucleus and motor neurons in the hamster spinal cord, the expression of the Cat-301 antigen requires neuronal activity during a circumscribed period in development. Disrupting the activity of Y-cells (by dark rearing or by monocular lid suture) or of motor neurons (by sciatic nerve crush or by spinal cord lesion) during the early postnatal period prevents Cat-301 expression. Disrupting neuronal activity in adults has no effect on Cat-301 expression. The onset of Cat-301 expression corresponds to the end of the period of activity-dependent development. In order to further dissect the components of the segmental reflex are required for the expression of Cat-301 on motor neurons, here we evaluated the effect of deafferentation by dorsal rhizotomy. In adult animals two weeks after deafferentation all sciatic motor neurons continue to express Cat-301. In contrast, in neonates two weeks after deafferentation the normal developmental expression of Cat-301 is reduced and less than 50% of sciatic motor neurons express Cat-301. We next selectively lesioned the small diameter afferents using the neurotoxin capsaicin. In contrast to rhizotomy, neonatal deletion of small diameter afferents has no effect on the development of Cat-301 expression on motor neurons. These results imply that input relayed by large diameter primary afferents (probably those conveying muscle and/or joint information) is required for normal maturation of motor neuronal properties during early life. They also provide further evidence for activity-dependent maturation of motor neurons.

MeSH Terms
Animals Antibodies, Monoclonal Calcitonin Gene-Related Peptide/metabolism Cricetinae Immunohistochemistry Membrane Proteins/metabolism Mesocricetus/metabolism,physiology Motor Neurons/metabolism,physiology Neurons, Afferent/physiology Proteoglycans/metabolism Sciatic Nerve/metabolism,physiology Spinal Cord/cytology,physiology
Chemicals
Antibodies, Monoclonal Membrane Proteins Proteoglycans Calcitonin Gene-Related Peptide
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Kalb R G
Section of Neuroanatomy, Yale University School of Medicine, New Haven, CT 06510.
Hockfield S
Article Info
Journal
Neuroscience
Abbr.
Neuroscience
ISSN
0306-4522
Published
1990-00-00
Pages
391-401
Language
English
Region
United States
NLM ID
7605074
Subset
IM
Grants
NEI NIH HHS · EY-06511 · United States
NINDS NIH HHS · NSO1247-O1 · United States
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