Single nigrostriatal dopaminergic neurons form widely spread and highly dense axonal arborizations in the neostriatum.

Matsuda W
Furuta T
Nakamura KC
Hioki H
Fujiyama F
Arai R
Kaneko T
Scientific Abstract

The axonal arbors of single nigrostriatal dopaminergic neurons were visualized with a viral vector expressing membrane-targeted green fluorescent protein in rat brain. All eight reconstructed tyrosine hydroxylase-positive dopaminergic neurons possessed widely spread and highly dense axonal arborizations in the neostriatum. All of them emitted very little axon collateral arborization outside of the striatum except for tiny arborization in the external pallidum. The striatal axonal bush of each reconstructed dopaminergic neuron covered 0.45-5.7% (mean +/- SD = 2.7 +/- 1.5%) of the total volume of the neostriatum. Furthermore, all the dopaminergic neurons innervated both striosome and matrix compartments of the neostriatum, although each neuron's arborization tended to favor one of these compartments. Our findings demonstrate that individual dopaminergic neurons of the substantia nigra can broadcast a dopamine signal and exert strong influence over a large number of striatal neurons. This divergent signaling should be a key to the function of the nigrostriatal system in dopamine-based learning and suggests that neurodegeneration of individual nigral neurons can affect multiple neurons in the striatum. Thus, these results would also contribute to understanding the clinicopathology of Parkinson's disease and related syndromes.

Citation

2009.J. Neurosci., 29(2):444-53.

Related Content
Publication
Dodson PD, Dreyer JK, Jennings K, Syed EC, Wade-Martins R, Cragg SJ, Bolam JP, Magill PJ
2016. Proc. Natl. Acad. Sci. U.S.A., 113(15):E2180-8.
Publication
Tinkhauser G, Pogosyan A, Tan H, Herz DM, Kühn AA, Brown P
2017. Brain, 140(11):2968-2981.
Publication
Abdi A, Mallet N, Mohamed FY, Sharott A, Dodson PD, Nakamura KC, Suri S, Avery SV, Larvin JT, Garas FN, Garas SN, Vinciati F, Morin S, Bezard E, Baufreton J, Magill PJ
2015. J. Neurosci., 35(17):6667-88.
Publication
Pristerà A, Lin WY, Kaufmann AK, Brimblecombe KR, Threlfell S, Dodson PD, Magill PJ, Fernandes C, Cragg SJ, Ang SL
2015.Proc. Natl. Acad. Sci. U.S.A., 112(35):E4929-38.