Ultrafast neuronal imaging of dopamine dynamics with designed genetically encoded sensors

Tommaso Patriarchi(University of California, Davis), Jounhong Ryan Cho(California Institute of Technology), Katharina Merten(Salk Institute for Biological Studies), Mark W. Howe(Northwestern University), Aaron Marley(University of California, San Francisco), Wei-Hong Xiong(Vollum Institute), Robert Folk(Salk Institute for Biological Studies), Gerard Joey Broussard(University of California, Davis), Ruqiang Liang(University of California, Davis), Min Jee Jang(California Institute of Technology), Haining Zhong(Vollum Institute), Daniel A. Dombeck(Northwestern University), Mark von Zastrow(University of California, San Francisco), Axel Nimmerjahn(Salk Institute for Biological Studies), Viviana Gradinaru(California Institute of Technology), John T. Williams(Vollum Institute), Lin Tian(University of California, Davis)
Science
May 31, 2018
Cited by 1,133Open Access
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Abstract

Neuromodulatory systems exert profound influences on brain function. Understanding how these systems modify the operating mode of target circuits requires spatiotemporally precise measurement of neuromodulator release. We developed dLight1, an intensity-based genetically encoded dopamine indicator, to enable optical recording of dopamine dynamics with high spatiotemporal resolution in behaving mice. We demonstrated the utility of dLight1 by imaging dopamine dynamics simultaneously with pharmacological manipulation, electrophysiological or optogenetic stimulation, and calcium imaging of local neuronal activity. dLight1 enabled chronic tracking of learning-induced changes in millisecond dopamine transients in mouse striatum. Further, we used dLight1 to image spatially distinct, functionally heterogeneous dopamine transients relevant to learning and motor control in mouse cortex. We also validated our sensor design platform for developing norepinephrine, serotonin, melatonin, and opioid neuropeptide indicators.


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