Ultrafast neuronal imaging of dopamine dynamics with designed genetically encoded sensors

Author:

Patriarchi Tommaso1ORCID,Cho Jounhong Ryan2ORCID,Merten Katharina3ORCID,Howe Mark W.4,Marley Aaron5,Xiong Wei-Hong6,Folk Robert W.3ORCID,Broussard Gerard Joey1,Liang Ruqiang1,Jang Min Jee2,Zhong Haining6ORCID,Dombeck Daniel4,von Zastrow Mark5ORCID,Nimmerjahn Axel3ORCID,Gradinaru Viviana2ORCID,Williams John T.6ORCID,Tian Lin1ORCID

Affiliation:

1. Department of Biochemistry and Molecular Medicine, University of California, Davis, 2700 Stockton Boulevard, Sacramento, CA 95817, USA.

2. Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.

3. Waitt Advanced Biophotonics Center, Salk Institute for Biological Studies, La Jolla, CA 92037, USA.

4. Department of Neurobiology, Northwestern University, Evanston, IL 60208, USA.

5. Department of Cellular and Molecular Pharmacology, University of California, San Francisco, CA 94131, USA.

6. Vollum Institute, Oregon Health & Science University, Portland, OR 97239, USA.

Abstract

Imaging dopamine release in the brain Neuromodulator release alters the function of target circuits in poorly known ways. An essential step to address this knowledge gap is to measure the dynamics of neuromodulatory signals while simultaneously manipulating the elements of the target circuit during behavior. Patriarchi et al. developed fluorescent protein–based dopamine indicators to visualize spatial and temporal release of dopamine directly with high fidelity and resolution. In the cortex, two-photon imaging with these indicators was used to map dopamine activity at cellular resolution. Science , this issue p. eaat4422

Funder

National Institutes of Health

NIH Office of the Director

National Institute on Aging

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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