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Circuit Architecture of VTA Dopamine Neurons Revealed by Systematic Input-Output Mapping.
Beier, Kevin T; Steinberg, Elizabeth E; DeLoach, Katherine E; Xie, Stanley; Miyamichi, Kazunari; Schwarz, Lindsay; Gao, Xiaojing J; Kremer, Eric J; Malenka, Robert C; Luo, Liqun.
Affiliation
  • Beier KT; Howard Hughes Medical Institute and Department of Biology, Stanford University, Stanford, CA 94305, USA; Nancy Pritzker Laboratory, Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, CA 94305, USA.
  • Steinberg EE; Nancy Pritzker Laboratory, Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, CA 94305, USA.
  • DeLoach KE; Howard Hughes Medical Institute and Department of Biology, Stanford University, Stanford, CA 94305, USA.
  • Xie S; Howard Hughes Medical Institute and Department of Biology, Stanford University, Stanford, CA 94305, USA.
  • Miyamichi K; Howard Hughes Medical Institute and Department of Biology, Stanford University, Stanford, CA 94305, USA.
  • Schwarz L; Howard Hughes Medical Institute and Department of Biology, Stanford University, Stanford, CA 94305, USA.
  • Gao XJ; Howard Hughes Medical Institute and Department of Biology, Stanford University, Stanford, CA 94305, USA.
  • Kremer EJ; Institut de Génétique Moléculaire de Montpellier, CNRS 5535, 34293 Montpellier, France; Université de Montpellier, 34000 Montpellier, France.
  • Malenka RC; Nancy Pritzker Laboratory, Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, CA 94305, USA. Electronic address: malenka@stanford.edu.
  • Luo L; Howard Hughes Medical Institute and Department of Biology, Stanford University, Stanford, CA 94305, USA. Electronic address: lluo@stanford.edu.
Cell ; 162(3): 622-34, 2015 Jul 30.
Article in En | MEDLINE | ID: mdl-26232228
ABSTRACT
Dopamine (DA) neurons in the midbrain ventral tegmental area (VTA) integrate complex inputs to encode multiple signals that influence motivated behaviors via diverse projections. Here, we combine axon-initiated viral transduction with rabies-mediated trans-synaptic tracing and Cre-based cell-type-specific targeting to systematically map input-output relationships of VTA-DA neurons. We found that VTA-DA (and VTA-GABA) neurons receive excitatory, inhibitory, and modulatory input from diverse sources. VTA-DA neurons projecting to different forebrain regions exhibit specific biases in their input selection. VTA-DA neurons projecting to lateral and medial nucleus accumbens innervate largely non-overlapping striatal targets, with the latter also sending extensive extra-striatal axon collaterals. Using electrophysiology and behavior, we validated new circuits identified in our tracing studies, including a previously unappreciated top-down reinforcing circuit from anterior cortex to lateral nucleus accumbens via VTA-DA neurons. This study highlights the utility of our viral-genetic tracing strategies to elucidate the complex neural substrates that underlie motivated behaviors.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ventral Tegmental Area / Neural Pathways / Neurons Limits: Animals Language: En Journal: Cell Year: 2015 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ventral Tegmental Area / Neural Pathways / Neurons Limits: Animals Language: En Journal: Cell Year: 2015 Document type: Article Affiliation country: United States