Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.
Sci. Signal., 5 October 2010
Vol. 3, Issue 142, p. ra73
[DOI: 10.1126/scisignal.2001128]
RESEARCH ARTICLES
Editor's Summary
A Swell Route to Neuronal Communication
Adenosine triphosphate (ATP), which can be released at synapses to act as a neurotransmitter, can also be released through mechanically activated anion channels in nonexcitable cells as part of a mechanism to restore volume under hypotonic conditions. Here, Fields and Ni show that minute increases in axon volume secondary to neuronal activity are associated with release of ATP from dorsal root ganglion (DRG) axons. This activity-dependent release of ATP was inhibited by preventing axonal swelling with hypertonic solutions, as well as by pharmacological blockade of various stretch-activated chloride channels, but not by agents that block the release of synaptic vesicles. Moreover, conditions that blocked ATP release also blocked signals from DRG neurons to cocultured astrocytes. The authors thus propose that nonvesicular release of signaling molecules through stretch-activated channels may represent a mechanism for activity-dependent communication between neurons and nearby cells.
Citation: R. D. Fields, Y. Ni, Nonsynaptic Communication Through ATP Release from Volume-Activated Anion Channels in Axons. Sci. Signal.3, ra73 (2010).
Elizabeth M. Adler (9 November 2010) Sci. Signal.3 (147), eg11.
[DOI: 10.1126/scisignal.3147eg11] |Abstract »|Full Text »|PDF »
PODCASTS
R. Douglas Fields and Annalisa M. VanHook (9 November 2010) Sci. Signal.3 (147), pc20.
[DOI: 10.1126/scisignal.3147pc20] |Abstract »|Full Text »|Podcast »
PERSPECTIVES
Klaus Ballanyi, Bogdan Panaitescu, and Araya Ruangkittisakul (9 November 2010) Sci. Signal.3 (147), pe41.
[DOI: 10.1126/scisignal.3147pe41] |Abstract »|Full Text »|PDF »|Movies »
Neurons respond directly to mechanical deformation with pannexin-mediated ATP release and autostimulation of P2X7 receptors.
J. Xia, J. C. Lim, W. Lu, J. M. Beckel, E. J. Macarak, A. M. Laties, and C. H. Mitchell (2012)
J. Physiol.
590, 2285-2304
|Abstract »|Full Text »|PDF »
Functional and Anatomical Identification of a Vesicular Transporter Mediating Neuronal ATP Release.
M. Larsson, K. Sawada, C. Morland, M. Hiasa, L. Ormel, Y. Moriyama, and V. Gundersen (2012)
Cereb Cortex
22, 1203-1214
|Abstract »|Full Text »|PDF »
Deletion of Ecto-5'-Nucleotidase (CD73) Reveals Direct Action Potential-Dependent Adenosine Release.
Engrailed homeoprotein recruits the adenosine A1 receptor to potentiate ephrin A5 function in retinal growth cones.
O. Stettler, R. L. Joshi, A. Wizenmann, J. Reingruber, D. Holcman, C. Bouillot, F. Castagner, A. Prochiantz, and K. L. Moya (2012)
Development
139, 215-224
|Abstract »|Full Text »|PDF »
Control of Local Protein Synthesis and Initial Events in Myelination by Action Potentials.