Environmental enrichment enhances synaptic plasticity by internalization of striatal dopamine transporters

Author:

Kim Myung-Sun12,Yu Ji Hea134,Kim Chul Hoon456,Choi Jae Yong57,Seo Jung Hwa14,Lee Min-Young12,Yi Chi Hoon8,Choi Tae Hyun8,Ryu Young Hoon7,Lee Jong Eun469,Lee Bae Hwan4610,Kim Hyongbum5,Cho Sung-Rae12411

Affiliation:

1. Department and Research Institute of Rehabilitation Medicine, Yonsei University College of Medicine, Seoul, Korea

2. Yonsei Stem Cell Center, Avison Biomedical Research Center, Seoul, Korea

3. Department of Medical Science, The Graduate School, Yonsei University, Seoul, Korea

4. Brain Korea 21 PLUS Project for Medical Science, Yonsei University, Seoul, Korea

5. Department of Pharmacology, Yonsei University College of Medicine, Seoul, Korea

6. Brain Research Institute, Yonsei University College of Medicine, Seoul, Korea

7. Department of Nuclear Medicine, Yonsei University College of Medicine, Seoul, Korea

8. Department of Molecular Imaging, Korea Institute of Radiological and Medical Sciences, Seoul, Korea

9. Department of Anatomy, Yonsei University College of Medicine, Seoul, Korea

10. Department of Physiology, Yonsei University College of Medicine, Seoul, Korea

11. Rehabilitation Institute of Neuromuscular Disease, Yonsei University College of Medicine, Seoul, Korea

Abstract

Environmental enrichment (EE) with a complex combination of physical, cognitive and social stimulations enhances synaptic plasticity and behavioral function. However, the mechanism remains to be elucidated in detail. We aimed to investigate dopamine-related synaptic plasticity underlying functional improvement after EE. For this, six-week-old CD-1 mice were randomly allocated to EE or standard conditions for two months. EE significantly enhanced behavioral functions such as rotarod and ladder walking tests. In a [18F]FPCIT positron emission tomography scan, binding values of striatal DAT were significantly decreased approximately 18% in the EE mice relative to the control mice. DAT inhibitor administrated to establish the relationship of the DAT down-regulation to the treatment effects also improved rotarod performances, suggesting that DAT inhibition recapitulated EE-mediated treatment benefits. Next, EE-induced internalization of DAT was confirmed using a surface biotinylation assay. In situ proximity ligation assay and immunoprecipitation demonstrated that EE significantly increased the phosphorylation of striatal DAT as well as the levels of DAT bound with protein kinase C (PKC). In conclusion, we suggest that EE enables phosphorylation of striatal DAT via a PKC-mediated pathway and causes DAT internalization. This is the first report to suggest an EE-mediated mechanism of synaptic plasticity by internalization of striatal DAT.

Publisher

SAGE Publications

Subject

Cardiology and Cardiovascular Medicine,Neurology (clinical),Neurology

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