Skip to main content

Main menu

  • HOME
  • CONTENT
    • Early Release
    • Featured
    • Current Issue
    • Issue Archive
    • Collections
    • Podcast
  • ALERTS
  • FOR AUTHORS
    • Information for Authors
    • Fees
    • Journal Clubs
    • eLetters
    • Submit
  • EDITORIAL BOARD
  • ABOUT
    • Overview
    • Advertise
    • For the Media
    • Rights and Permissions
    • Privacy Policy
    • Feedback
  • SUBSCRIBE

User menu

  • Log in
  • My Cart

Search

  • Advanced search
Journal of Neuroscience
  • Log in
  • My Cart
Journal of Neuroscience

Advanced Search

Submit a Manuscript
  • HOME
  • CONTENT
    • Early Release
    • Featured
    • Current Issue
    • Issue Archive
    • Collections
    • Podcast
  • ALERTS
  • FOR AUTHORS
    • Information for Authors
    • Fees
    • Journal Clubs
    • eLetters
    • Submit
  • EDITORIAL BOARD
  • ABOUT
    • Overview
    • Advertise
    • For the Media
    • Rights and Permissions
    • Privacy Policy
    • Feedback
  • SUBSCRIBE
PreviousNext
Articles

Local role of Ca2+ in formation of veils in growth cones

DJ Goldberg
Journal of Neuroscience 1 July 1988, 8 (7) 2596-2605; DOI: https://doi.org/10.1523/JNEUROSCI.08-07-02596.1988
DJ Goldberg
Department of Pharmacology, Columbia University, College of Physicians and Surgeons, New York, New York 10032.
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • Article
  • Info & Metrics
  • eLetters
  • PDF
Loading

Abstract

A previous study that used high-resolution video (VEC-DIC) microscopy to examine axonal growth cones of Aplysia giant neurons growing in culture had demonstrated that growth occurs by the extension of veils of membrane between filopodia and the subsequent morphological transformation of these veils, in place, into the swollen, organelle- filled central region of the growth cone and then into the cylindrical axon. The possible involvement of Ca2+ in this sequence of events was now examined using VEC-DIC microscopy. Reduction of [Ca2+]o from the normal level of 11 to 1.3 mM or below or the addition of 20 mM Co2+, which blocks Ca2+ channels, caused a large decrease in the area of immature veil (flat and with few organelles) in the growth cone within minutes. Ba2+, 20 mM, which flows well through Ca2+ channels, and 5 microM A23187, a Ca2+ ionophore, caused new immature veil to form in the presence of reduced [Ca2+]o. Maturation of veil into central region was not inhibited by reduced [Ca2+]o. In fact, the disappearance of immature veil was often the result partly, or entirely, of continued veil maturation in the absence of formation of new veil. The next step in maturation, conversion of the central region to cylindrical axon, was also probably not inhibited by reduced [Ca2+]o. Ca2+ was microapplied to large growth cones that had lost their veils by exposure to reduced [Ca2+]o. There was a strong tendency for the first, or only, incidence of veil formation to occur near the micropipette, the rest of the perimeter of the growth cone remaining quiescent. It is concluded that intracellular Ca2+ plays a role in veil formation and that the site of the Ca2+-dependent step is close to the site of veil formation. If this step is exocytosis, veil forms where there is net addition of membrane. Whether a change in [Ca2+]i, rather than some other factor, normally directly triggers veil formation remains uncertain, but, if it does, then the site of formation, which will strongly influence the direction of axon growth, is probably determined by focal changes in [Ca2+]i within the growth cone.

Back to top

In this issue

The Journal of Neuroscience: 8 (7)
Journal of Neuroscience
Vol. 8, Issue 7
1 Jul 1988
  • Table of Contents
  • Table of Contents (PDF)
  • Index by author
Email

Thank you for sharing this Journal of Neuroscience article.

NOTE: We request your email address only to inform the recipient that it was you who recommended this article, and that it is not junk mail. We do not retain these email addresses.

Enter multiple addresses on separate lines or separate them with commas.
Local role of Ca2+ in formation of veils in growth cones
(Your Name) has forwarded a page to you from Journal of Neuroscience
(Your Name) thought you would be interested in this article in Journal of Neuroscience.
CAPTCHA
This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.
View Full Page PDF
Citation Tools
Local role of Ca2+ in formation of veils in growth cones
DJ Goldberg
Journal of Neuroscience 1 July 1988, 8 (7) 2596-2605; DOI: 10.1523/JNEUROSCI.08-07-02596.1988

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero
Respond to this article
Request Permissions
Share
Local role of Ca2+ in formation of veils in growth cones
DJ Goldberg
Journal of Neuroscience 1 July 1988, 8 (7) 2596-2605; DOI: 10.1523/JNEUROSCI.08-07-02596.1988
del.icio.us logo Digg logo Reddit logo Twitter logo CiteULike logo Facebook logo Google logo Mendeley logo
  • Tweet Widget
  • Facebook Like
  • Google Plus One

Jump to section

  • Article
  • Info & Metrics
  • eLetters
  • PDF

Responses to this article

Respond to this article

Jump to comment:

No eLetters have been published for this article.

Related Articles

Cited By...

More in this TOC Section

  • Choice Behavior Guided by Learned, But Not Innate, Taste Aversion Recruits the Orbitofrontal Cortex
  • Maturation of Spontaneous Firing Properties after Hearing Onset in Rat Auditory Nerve Fibers: Spontaneous Rates, Refractoriness, and Interfiber Correlations
  • Insulin Treatment Prevents Neuroinflammation and Neuronal Injury with Restored Neurobehavioral Function in Models of HIV/AIDS Neurodegeneration
Show more Articles
  • Home
  • Alerts
  • Visit Society for Neuroscience on Facebook
  • Follow Society for Neuroscience on Twitter
  • Follow Society for Neuroscience on LinkedIn
  • Visit Society for Neuroscience on Youtube
  • Follow our RSS feeds

Content

  • Early Release
  • Current Issue
  • Issue Archive
  • Collections

Information

  • For Authors
  • For Advertisers
  • For the Media
  • For Subscribers

About

  • About the Journal
  • Editorial Board
  • Privacy Policy
  • Contact
(JNeurosci logo)
(SfN logo)

Copyright © 2023 by the Society for Neuroscience.
JNeurosci Online ISSN: 1529-2401

The ideas and opinions expressed in JNeurosci do not necessarily reflect those of SfN or the JNeurosci Editorial Board. Publication of an advertisement or other product mention in JNeurosci should not be construed as an endorsement of the manufacturer’s claims. SfN does not assume any responsibility for any injury and/or damage to persons or property arising from or related to any use of any material contained in JNeurosci.