The growth of single sympathetic neurons in tissue culture was examined with particular regard to the way in which the patterns of axonal or dendritic processes (here called nerve fibers), were formed. The tips of the fibers were seen to advance in straight lines and to grow at rates that did not vary appreciably with time, with their position in the cell outgrowth, or with the fiber diameter. Most of the branch points were formed by the bifurcation of a fiber tip (growth cone), apparently at random, and thereafter remained at about the same distance from the cell body. It seemed that the final shape of a neuron was the result of the reiterated and largely autonomous activities of the growth cones. The other parts of the cell played a supportive role but, apart from this, had no obvious influence on the final pattern of branches formed.
Skip Nav Destination
Article navigation
1 March 1973
Article|
March 01 1973
BRANCHING PATTERNS OF INDIVIDUAL SYMPATHETIC NEURONS IN CULTURE
D. Bray
D. Bray
From The Department of Neurobiology, Harvard Medical School, Boston, Massachusetts 02115.
Search for other works by this author on:
D. Bray
From The Department of Neurobiology, Harvard Medical School, Boston, Massachusetts 02115.
Dr. Bray's present address is The Medical Research Council, Laboratory of Molecular Biology, Cambridge, England.
Received:
July 31 1972
Revision Received:
September 14 1972
Online ISSN: 1540-8140
Print ISSN: 0021-9525
Copyright © 1973 by The Rockefeller University Press
1973
J Cell Biol (1973) 56 (3): 702–712.
Article history
Received:
July 31 1972
Revision Received:
September 14 1972
Citation
D. Bray; BRANCHING PATTERNS OF INDIVIDUAL SYMPATHETIC NEURONS IN CULTURE . J Cell Biol 1 March 1973; 56 (3): 702–712. doi: https://doi.org/10.1083/jcb.56.3.702
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