Document Detail


Cultivation of rat fetal spinal cord slices in a semi-solid medium: a new approach to studying axonal outgrowth and regeneration.
MedLine Citation:
PMID:  1921469     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
A soft agar culture system was used for the cultivation of spinal cord slices with the purpose of improving the evaluation of the dynamics of axonal outgrowth and development. Slices of the spinal cord of 15-day-old fetal Wistar rats were cultured in a 0.5% agar culture medium. The sprouting and outgrowth of axons from the slices was observed at 6-24-h intervals. The morphology and growth rates of axons could be easily investigated by light microscopy. Quantification of growth parameters of individual neurites is made easy because no cells migrate out of the slices, so that the outgrowth is not masked by migrating neurons, fibroblasts, glial cells etc. The axons had well-developed growth cones, comparable to those observed in liquid medium; the daily growth rate was on average 318 microns during the 6 days of observation, with a maximum of 1050 microns per day. Back-labelling with a fluorescent dye (DiI) indicated that the longest neurites originated from motoneurons. Our experiments show that axons can develop and grow in a soft agar medium without the need for adding any growth promoting factor or substrate molecule.
Authors:
V Mandys; R van der Neut; P R Bär; W H Gispen
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Journal of neuroscience methods     Volume:  38     ISSN:  0165-0270     ISO Abbreviation:  J. Neurosci. Methods     Publication Date:  1991 Jun 
Date Detail:
Created Date:  1991-11-12     Completed Date:  1991-11-12     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  7905558     Medline TA:  J Neurosci Methods     Country:  NETHERLANDS    
Other Details:
Languages:  eng     Pagination:  63-9     Citation Subset:  IM    
Affiliation:
Institute of Experimental Medicine, Czechoslovak Academy of Sciences, Prague.
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MeSH Terms
Descriptor/Qualifier:
Agar
Animals
Axons / physiology*
Culture Media
Culture Techniques
Fetus
Histological Techniques*
Nerve Regeneration / physiology*
Rats
Rats, Inbred Strains
Spinal Cord / cytology,  embryology*,  ultrastructure
Time Factors
Chemical
Reg. No./Substance:
0/Culture Media; 9002-18-0/Agar

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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