Home LiteratureArticle Details
PMID: 8454738 Published · ppublish English Comparative Study 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.

Differential expression of neuron-glia cell adhesion molecule (Ng-CAM) on developing axons and growth cones of interneurons in the chick embryo spinal cord: an immunoelectron microscopic study.

The Journal of comparative neurology ·Vol. 329 ·No. 4 ·1993-03-22 ·Pages 512-8

Shiga T, Shirai T, Grumet M, Edelman GM, Oppenheim RW

Abstract

To elucidate the role of neuron-glia cell adhesion molecule (Ng-CAM) in axonal pathway formation of avian spinal interneurons, we have examined the ultrastructural expression of Ng-CAM in the developing spinal cord, by using a preembedding immunocytochemical method. Ng-CAM immunoreactivity was punctate and was restricted to cell surfaces. In accordance with our previous light microscopic observations (Shiga et al., '90), the earliest developing spinal interneurons were Ng-CAM-positive on their cell bodies, axons, and growth cones. Axons and growth cones that were either fasciculated or in contact with each other strongly expressed Ng-CAM, thus indicating the possible involvement of Ng-CAM in fasciculation of axons and in the contact guidance of growth cones along preexisting axons. By using higher resolution immunoelectron microscopy, the present study has also revealed new information on the subcellular localization of Ng-CAM on developing spinal interneurons, neuroepithelial cells, and floor plate cells. Although Ng-CAM immunoreactivity was prominent on both axons and growth cones, these structures were Ng-CAM-negative when they contacted the basal lamina around the spinal cord. By contrast, Ng-CAM was detectable on the surface of both neuroepithelial cells and floor plate cells only when they made contact with the Ng-CAM-positive axons and growth cones of interneurons. These results suggest that the subcellular distribution of Ng-CAM is regulated differentially, depending on the apposing cell surfaces, and that such differential and developmentally regulated expression may contribute to the elongation, fasciculation, and guidance of spinal axons.

MeSH Terms
Animals Axons/chemistry Cell Adhesion Molecules, Neuronal/analysis Chick Embryo/innervation,metabolism Embryonic and Fetal Development/physiology Interneurons/chemistry,ultrastructure Microscopy, Immunoelectron Neural Pathways/ultrastructure Spinal Cord/embryology,metabolism
Chemicals
Cell Adhesion Molecules, Neuronal
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Shiga T
Department of Neurobiology and Anatomy, Bowman Gray School of Medicine, Wake Forest University, Winston-Salem, North Carolina 27156.
Shirai T
Grumet M
Edelman G M
Oppenheim R W
Article Info
Journal
The Journal of comparative neurology
Abbr.
J Comp Neurol
ISSN
0021-9967
Published
1993-03-22
Pages
512-8
Language
English
Region
United States
NLM ID
0406041
Subset
IM
Grants
NINDS NIH HHS · NS20402 · United States
NINDS NIH HHS · NS21629 · United States
NINDS NIH HHS · NS22789 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com