Published April 20, 2016 | Version Accepted Version + Supplemental Material
Journal Article Open

Cholinergic Mesopontine Signals Govern Locomotion and Reward through Dissociable Midbrain Pathways

Abstract

The mesopontine tegmentum, including the pedunculopontine and laterodorsal tegmental nuclei (PPN and LDT), provides major cholinergic inputs to midbrain and regulates locomotion and reward. To delineate the underlying projection-specific circuit mechanisms, we employed optogenetics to control mesopontine cholinergic neurons at somata and at divergent projections within distinct midbrain areas. Bidirectional manipulation of PPN cholinergic cell bodies exerted opposing effects on locomotor behavior and reinforcement learning. These motor and reward effects were separable via limiting photostimulation to PPN cholinergic terminals in the ventral substantia nigra pars compacta (vSNc) or to the ventral tegmental area (VTA), respectively. LDT cholinergic neurons also form connections with vSNc and VTA neurons; however, although photo-excitation of LDT cholinergic terminals in the VTA caused positive reinforcement, LDT-to-vSNc modulation did not alter locomotion or reward. Therefore, the selective targeting of projection-specific mesopontine cholinergic pathways may offer increased benefit in treating movement and addiction disorders.

Additional Information

© 2016 Elsevier. Received 19 October 2015, Revised 10 February 2016, Accepted 18 March 2016, Available online 20 April 2016. Published: April 20, 2016. We thank the entire V.G. lab for helpful discussions and Drs. David J. Anderson and Henry A. Lester for helpful comments on the manuscript. This work was supported by grants to V.G.: NIH Director's New Innovator IDP20D017782-01 and PECASE; NIH/NIA 1R01AG047664-01 (C.X. is a co-investigator); NIH BRAIN 1U01NS090577; Heritage Medical Research Institute; Pew Charitable Trust; Michael J. Fox Foundation; Sloan Foundation; as well as by funding support from the Beckman Institute for the Resource Center on CLARITY, Optogenetics, and Vector Engineering for technology development and broad dissemination (http://www.beckmaninstitute.caltech.edu/clover.shtml). Work in the V.G. Laboratory at Caltech is also funded by the following awards (to V.G.): NIH/NIMH 1R21MH103824-01; Kimmel Foundation; Human Frontiers in Science Program; Mallinckrodt Foundation; Gordon and Betty Moore Foundation through Grant GBMF2809 to the Caltech Programmable Molecular Technology Initiative; Caltech-GIST; Caltech-CBEA; Caltech-CEMI; Caltech-City of Hope Biomedical Initiative. C.X. is partly supported by Michael J. Fox Foundation. J.B.T. acknowledges the Colvin Postdoctoral Fellowship. K.C. is supported by the NIH Predoctoral Training in Biology and Chemistry (2T32GM007616-36).

Attached Files

Accepted Version - nihms774500.pdf

Supplemental Material - mmc1.pdf

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Additional details

Identifiers

PMCID
PMC4840478
Eprint ID
66298
Resolver ID
CaltechAUTHORS:20160420-090626768

Funding

NIH
IDP20D017782-01
NSF
NIH
1R01AG047664-01
NIH
1U01NS090577
Heritage Medical Research Institute
Pew Charitable Trust
Michael J. Fox Foundation
Alfred P. Sloan Foundation
Caltech Beckman Institute
NIH
1R21MH103824-01
Sidney Kimmel Foundation for Cancer Research
Human Frontier Science Program
Edward Mallinckrodt, Jr. Foundation
Gordon and Betty Moore Foundation
GBMF2809
Caltech-GIST SURF Exchange Program
Amgen
Caltech Center for Environmental Microbial Interactions (CEMI)
Caltech-City of Hope Biomedical Initiative
Colvin Postdoctoral Fellowship
NIH Predoctoral Fellowship
2T32GM007616-36
Caltech Summer Undergraduate Research Fellowship (SURF)

Dates

Created
2016-04-20
Created from EPrint's datestamp field
Updated
2022-04-28
Created from EPrint's last_modified field