Publication

Dopaminergic neurons intrinsic to the primate striatum

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Last modified
  • 05/15/2025
Type of Material
Authors
    Ranjita Betarbet, Emory UniversityRobert Turner, Emory UniversityVijay Chockkan, Emory UniversityMahlon R DeLong, Emory UniversityKelly A. Allers, Emory UniversityJudith Walters, National Institute of Neurological Disorders and StrokeAllan I Levey, Emory UniversityJ. Timothy Greenamyre, Emory University
Language
  • English
Date
  • 1997-09-01
Publisher
  • Lippincott, Williams & Wilkins
Publication Version
Copyright Statement
  • Copyright © 1997 Society for Neuroscience
License
Final Published Version (URL)
Title of Journal or Parent Work
ISSN
  • 0888-0395
Volume
  • 17
Issue
  • 17
Start Page
  • 6761
End Page
  • 6768
Grant/Funding Information
  • This work was supported by United States Public Health Service Grants NS33779 (J.T.G.) and NS31937 (A.I.L. and M.R.D.); and a Mallinckrodt Scholar Award (J.T.G.).
Abstract
  • Intrinsic, striatal tyrosine hydroxylase-immunoreactive (TH-i) cells have received little consideration. In this study we have characterized these neurons and their regulatory response to nigrostriatal dopaminergic deafferentation. TH-i cells were observed in the striatum of both control and 1-methyl-4-phenyl-1,2,3, 6-tetrahydropyridine (MPTP)-treated monkeys; TH-i cell counts, however, were 3.5-fold higher in the striatum of MPTP-lesioned monkeys. To establish the dopaminergic nature of the TH-i cells, sections were double-labeled with antibodies to dopamine transporter (DAT). Immunofluorescence studies demonstrated that nearly all TH-i cells were double-labeled with DAT, suggesting that they contain the machinery to be functional dopaminergic neurons. Two types of TH-i cells were identified in the striatum: small, aspiny, bipolar cells with varicose dendrites and larger spiny, multipolar cells. The aspiny cells, which were more prevalent, corresponded morphologically to the GABAergic interneurons of the striatum. Double-label immunofluorescence studies using antibodies to TH and glutamate decarboxylase (GAD67), the synthetic enzyme for GABA, showed that 99% of the TH-i cells were GAD67-positive. Very few (<1%) of the TH-i cells, however, were immunoreactive for the calcium-binding proteins calbindin and parvalbumin. In summary, these results demonstrate that the dopaminergic cell population of the striatum responds to dopamine denervation by increasing in number, apparently to compensate for loss of extrinsic dopaminergic innervation. Moreover, this population of cells corresponds largely with the intrinsic GABAergic cells of the striatum. This study also suggests that the adult primate striatum does retain some intrinsic capacity to compensate for dopaminergic cell loss.
Author Notes
  • Dr. J. Timothy Greenamyre, Department of Neurology, Emory University, 1639 Pierce Drive, WMB 6000, Atlanta, GA 30322
Keywords
Research Categories
  • Biology, Neuroscience
  • Health Sciences, Pharmacology

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