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.


Originally published in Science Express on 6 March 2008
Science 18 April 2008:
Vol. 320. no. 5874, pp. 369 - 373
DOI: 10.1126/science.1152677

Reports

A Model for Neuronal Competition During Development

Christopher D. Deppmann,1,2* Stefan Mihalas,1,3* Nikhil Sharma,1,2* Bonnie E. Lonze,1,2 Ernst Niebur,1,3 David D. Ginty1,2{dagger}

We report that developmental competition between sympathetic neurons for survival is critically dependent on a sensitization process initiated by target innervation and mediated by a series of feedback loops. Target-derived nerve growth factor (NGF) promoted expression of its own receptor TrkA in mouse and rat neurons and prolonged TrkA-mediated signals. NGF also controlled expression of brain-derived neurotrophic factor and neurotrophin-4, which, through the receptor p75, can kill neighboring neurons with low retrograde NGF-TrkA signaling whereas neurons with high NGF-TrkA signaling are protected. Perturbation of any of these feedback loops disrupts the dynamics of competition. We suggest that three target-initiated events are essential for rapid and robust competition between neurons: sensitization, paracrine apoptotic signaling, and protection from such effects.

1 The Solomon Snyder Department of Neuroscience, The Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
2 Howard Hughes Medical Institute, The Johns Hopkins University School of Medicine, Baltimore, MD21205, USA.
3 The Zanvyl Krieger Mind/Brain Institute, The Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.

* These authors contributed equally to this work.

{dagger} To whom correspondence should be addressed. E-mail: dginty{at}jhmi.edu

Read the Full Text



THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
Nuclear Factor of Activated T-Cells Isoform c4 (NFATc4/NFAT3) as a Mediator of Antiapoptotic Transcription in NMDA Receptor-Stimulated Cortical Neurons.
A. Vashishta, A. Habas, P. Pruunsild, J.-J. Zheng, T. Timmusk, and M. Hetman (2009)
J. Neurosci. 29, 15331-15340
   Abstract »    Full Text »    PDF »
Axonal Targeting of Trk Receptors via Transcytosis Regulates Sensitivity to Neurotrophin Responses.
M. Ascano, A. Richmond, P. Borden, and R. Kuruvilla (2009)
J. Neurosci. 29, 11674-11685
   Abstract »    Full Text »    PDF »
Fates of Neurotrophins after Retrograde Axonal Transport: Phosphorylation of p75NTR Is a Sorting Signal for Delayed Degradation.
R. Butowt and C. S. von Bartheld (2009)
J. Neurosci. 29, 10715-10729
   Abstract »    Full Text »    PDF »



To Advertise     Find Products


Science. ISSN 0036-8075 (print), 1095-9203 (online)