J Physiol Wellcome Trust-funded researchers
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Physiol Vol 314 pp 121-135
Copyright © 1981 by The Physiological Society
This Article
Right arrow Full Text (PDF)
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Hinkle, L
Right arrow Articles by Robinson, K R
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hinkle, L
Right arrow Articles by Robinson, K R

The direction of growth of differentiating neurones and myoblasts from frog embryos in an applied electric field.

L Hinkle, C D McCaig and K R Robinson

1. Disaggregated single neurones and myoblasts obtained from the neural tube and somites of Xenopus laevis embryos (stages 17-21) were cultured in the presence of steady small electric fields. 2. Neurites grew preferentially towards the negative pole, or cathode, in field strengths of 7-190 mV/mm. Many turned through considerable angles to do so. This effect disappeared below a threshold level of about 7 mV/mm. 3. Greater numbers of neurones sprouted neurites in cultures exposed to an electric field compared to control cultures. The difference could be as much as tenfold. The threshold level of this phenomenon was about 6-8 mV/mm. Other cell types such as pigment cells and fibroblasts were also stimulated to differentiate in culture by an electric field, although to a lesser extent than neurones. 4. Applied electric fields had no effect on the location of the origin of neurites on the cell body. 5. Spherical myoblasts cultured in applied electric fields (36-170 mV/mm) elongated with a bipolar axis of growth which was perpendicular to the electric field. The response was graded and disappeared at field strengths below 36 mV/mm. 6. It is suggested that in vivo, the direction of neural outgrowth from the neural tube and the strict spatial organization of somites might be under the control, in part, of endogenous electric fields. Possible sources of these are discussed.




This article has been cited by other articles:


Home page
DevelopmentHome page
D. S. Adams, A. Masi, and M. Levin
H+ pump-dependent changes in membrane voltage are an early mechanism necessary and sufficient to induce Xenopus tail regeneration
Development, April 1, 2007; 134(7): 1323 - 1335.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
A. M. Rajnicek, L. E. Foubister, and C. D. McCaig
Temporally and spatially coordinated roles for Rho, Rac, Cdc42 and their effectors in growth cone guidance by a physiological electric field
J. Cell Sci., May 1, 2006; 119(9): 1723 - 1735.
[Abstract] [Full Text] [PDF]


Home page
FASEB J.Home page
B. Reid, B. Song, C. D. McCaig, and M. Zhao
Wound healing in rat cornea: the role of electric currents
FASEB J, March 1, 2005; 19(3): 379 - 386.
[Abstract] [Full Text] [PDF]


Home page
IOVSHome page
V. A. McBain, J. V. Forrester, and C. D. McCaig
HGF, MAPK, and a Small Physiological Electric Field Interact during Corneal Epithelial Cell Migration
Invest. Ophthalmol. Vis. Sci., February 1, 2003; 44(2): 540 - 547.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
T. M. Brushart, P. N. Hoffman, R. M. Royall, B. B. Murinson, C. Witzel, and T. Gordon
Electrical Stimulation Promotes Motoneuron Regeneration without Increasing Its Speed or Conditioning the Neuron
J. Neurosci., August 1, 2002; 22(15): 6631 - 6638.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Biol.Home page
M. Zhao, T. Jin, C. D. McCaig, J. V. Forrester, and P. N. Devreotes
Genetic analysis of the role of G protein-coupled receptor signaling in electrotaxis
J. Cell Biol., June 10, 2002; 157(6): 921 - 928.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
F. Strata, M. Atzori, M. Molnar, G. Ugolini, F. Tempia, and E. Cherubini
A Pacemaker Current in Dye-Coupled Hilar Interneurons Contributes to the Generation of Giant GABAergic Potentials in Developing Hippocampus
J. Neurosci., February 15, 1997; 17(4): 1435 - 1446.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1981 The Physiological Society.