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.
GoGreen Membership

Site Tools

  • AAAS
  • Subscribe
  • Feedback

Site Search

Search Advanced

Science 20 April 2007:
Vol. 316. no. 5823, pp. 457 - 460
DOI: 10.1126/science.1139438

Reports

Neuronal Competition and Selection During Memory Formation

Jin-Hee Han,1,2,3* Steven A. Kushner,4,5,6* Adelaide P. Yiu,1,3 Christy J. Cole,1,2 Anna Matynia,4 Robert A. Brown,4 Rachael L. Neve,7 John F. Guzowski,8 Alcino J. Silva,4 Sheena A. Josselyn1,2,3{dagger}

Competition between neurons is necessary for refining neural circuits during development and may be important for selecting the neurons that participate in encoding memories in the adult brain. To examine neuronal competition during memory formation, we conducted experiments with mice in which we manipulated the function of CREB (adenosine 3',5'-monophosphate response element–binding protein) in subsets of neurons. Changes in CREB function influenced the probability that individual lateral amygdala neurons were recruited into a fear memory trace. Our results suggest a competitive model underlying memory formation, in which eligible neurons are selected to participate in a memory trace as a function of their relative CREB activity at the time of learning.

1 Program in Neurosciences and Mental Health, Hospital for Sick Children, 555 University Avenue, Toronto, Ontario M5G 1X8, Canada.
2 Department of Physiology, University of Toronto, Toronto, Ontario M5S 1A8, Canada.
3 Institute of Medical Sciences, University of Toronto, Toronto, Ontario M5S 1A8, Canada.
4 Departments of Neurobiology, Psychology, and Psychiatry, and Brain Research Institute, Gonda Building, 695 Young Drive South, University of California, Los Angeles, CA 90095, USA.
5 Department of Psychiatry, Columbia University, New York, NY 10032, USA.
6 New York State Psychiatric Institute, New York, NY 10032, USA.
7 Molecular Neurogenetics Laboratory, Department of Psychiatry, Harvard Medical School, McLean Hospital, Belmont, MA 02478, USA.
8 Neurobiology and Behavior, School of Biological Sciences, University of California, Irvine, CA 92697, USA.

* These authors contributed equally to this work.

{dagger} To whom correspondence should be addressed. E-mail: sheena.josselyn{at}sickkids.ca

Read the Full Text



THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
CREB has a context-dependent role in activity-regulated transcription and maintains neuronal cholesterol homeostasis.
T. Lemberger, J. R. Parkitna, M. Chai, G. Schutz, and D. Engblom (2008)
FASEB J 22, 2872-2879
   Abstract »    Full Text »    PDF »
Increasing CREB in the auditory thalamus enhances memory and generalization of auditory conditioned fear.
J.-H. Han, A. P. Yiu, C. J. Cole, H.-L. Hsiang, R. L. Neve, and S. A. Josselyn (2008)
Learn. Mem. 15, 443-453
   Abstract »    Full Text »    PDF »
BDNF is essential to promote persistence of long-term memory storage.
P. Bekinschtein, M. Cammarota, C. Katche, L. Slipczuk, J. I. Rossato, A. Goldin, I. Izquierdo, and J. H. Medina (2008)
PNAS 105, 2711-2716
   Abstract »    Full Text »    PDF »
NEURONS VIE FOR RECRUITMENT.
S. Sangha (2007)
J. Exp. Biol. 210, v-vi
   Full Text »    PDF »
Highlights From The Literature.
(2007)
Physiology 22, 231-233
   Full Text »    PDF »
Temporal requirement of C/EBP{beta} in the amygdala following reactivation but not acquisition of inhibitory avoidance.
M. H. Milekic, G. Pollonini, and C. M. Alberini (2007)
Learn. Mem. 14, 504-511
   Abstract »    Full Text »    PDF »



ADVERTISEMENT
Click Me!

ADVERTISEMENT
Click Me!

To Advertise     Find Products


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