A critical time window for dopamine actions on the structural plasticity of dendritic spines.

Sho Yagishita, Akiko Hayashi-Takagi, Graham C R Ellis-Davies, Hidetoshi Urakubo, Shin Ishii, Haruo Kasai
Author Information
  1. Sho Yagishita: Laboratory of Structural Physiology, Center for Disease Biology and Integrative Medicine, Faculty of Medicine, The University of Tokyo, Bunkyo-ku, Tokyo 113-0033, Japan. Core Research for Evolutional Science and Technology, Japan Science and Technology Agency, Japan Science and Technology Agency, 4-1-8 Honcho, Kawaguchi, Saitama 332-0012, Japan.
  2. Akiko Hayashi-Takagi: Laboratory of Structural Physiology, Center for Disease Biology and Integrative Medicine, Faculty of Medicine, The University of Tokyo, Bunkyo-ku, Tokyo 113-0033, Japan. Core Research for Evolutional Science and Technology, Japan Science and Technology Agency, Japan Science and Technology Agency, 4-1-8 Honcho, Kawaguchi, Saitama 332-0012, Japan. Precursory Research for Embryonic Science and Technology, Japan Science and Technology Agency, Japan Science and Technology Agency, 4-1-8 Honcho, Kawaguchi, Saitama 332-0012, Japan.
  3. Graham C R Ellis-Davies: Department of Neuroscience, Mount Sinai School of Medicine, New York, NY 10029, USA.
  4. Hidetoshi Urakubo: Integrated Systems Biology Laboratory, Department of Systems Science, Graduate School of Informatics, Kyoto University, Sakyo-ku, Kyoto 606-8501, Japan.
  5. Shin Ishii: Integrated Systems Biology Laboratory, Department of Systems Science, Graduate School of Informatics, Kyoto University, Sakyo-ku, Kyoto 606-8501, Japan.
  6. Haruo Kasai: Laboratory of Structural Physiology, Center for Disease Biology and Integrative Medicine, Faculty of Medicine, The University of Tokyo, Bunkyo-ku, Tokyo 113-0033, Japan. Core Research for Evolutional Science and Technology, Japan Science and Technology Agency, Japan Science and Technology Agency, 4-1-8 Honcho, Kawaguchi, Saitama 332-0012, Japan. hkasai@m.u-tokyo.ac.jp.

Abstract

Animal behaviors are reinforced by subsequent rewards following within a narrow time window. Such reward signals are primarily coded by dopamine, which modulates the synaptic connections of medium spiny neurons in the striatum. The mechanisms of the narrow timing detection, however, remain unknown. Here, we optically stimulated dopaminergic and glutamatergic inputs separately and found that dopamine promoted spine enlargement only during a narrow time window (0.3 to 2 seconds) after the glutamatergic inputs. The temporal contingency was detected by rapid regulation of adenosine 3',5'-cyclic monophosphate in thin distal dendrites, in which protein-kinase A was activated only within the time window because of a high phosphodiesterase activity. Thus, we describe a molecular basis of reinforcement plasticity at the level of single dendritic spines.

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Grants

  1. GM53395/NIGMS NIH HHS
  2. DA035612/NIDA NIH HHS
  3. NS069720/NINDS NIH HHS
  4. R21 DA035612/NIDA NIH HHS
  5. R01 NS069720/NINDS NIH HHS
  6. R01 GM053395/NIGMS NIH HHS

MeSH Term

Animals
Cyclic AMP
Cyclic AMP-Dependent Protein Kinases
Dendritic Spines
Dopamine
Dopamine Plasma Membrane Transport Proteins
Electrical Synapses
Glutamic Acid
Learning
Mice
Neuronal Plasticity
Phosphoric Diester Hydrolases
Reward
Time Factors

Chemicals

Dopamine Plasma Membrane Transport Proteins
Glutamic Acid
Cyclic AMP
Cyclic AMP-Dependent Protein Kinases
Phosphoric Diester Hydrolases
Dopamine

Word Cloud

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