2005 Fiscal Year Final Research Report Summary
Localization of high affinity choline transporter in the primate nervous system.
| Project/Area Number |
15500246
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Nerve anatomy/Neuropathology
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| Research Institution | Kyorin University |
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Principal Investigator |
MATSUMURA George Kyorin University, School of Medicine, Department of Anatomy, Professor, 医学部, 教授 (90173880)
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| Co-Investigator(Kenkyū-buntansha) |
KOBAYASHI Yasushi National Defense Medical College, Department of Anatomy and Neurobiology, Professor, 医学教育部, 教授 (00195819)
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| Project Period (FY) |
2003 – 2005
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| Keywords | primate / central nervous system / neuromuscular junction / in situ hybridization / immunohistochemistry / electron microscopy / acetylcholine / transporter |
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| Research Abstract |
1.Localization in the central nervous system
Using in situ hybridization and immunohistochemistry, we have determined the localization of high affinity choline transporter (CHT) messenger RNA and protein in the macaque monkey central nervous system. Signals for CHT mRNA and protein are localized in neurons in the motor nuclei of the cranial nerves (somatic motor and parasympathetic preganglionic), laterodorsal tegmental nucleus, parabrachial nucleus, pedunculopontine tegmental nucleus, globus pallidus, neostriatum, nucleus accumbens, nucleus of the diagonal band of Broca, nucleus basalis of Meynert, medial septal nucleus, and olfactory tubercle. Parasympathetic preganglionic neurons exhibited significantly lower density of CHT mRNA and protein than other positive neurons. In the spinal cord, motor neurons in the ventral horn showed both signals for CHT mRNA and protein. Putative gamma-motor neurons always showed strong immunoreactivity for CHT, while putative alpha-motor neurons showed
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wide variety of immunoreactivity intensities. Of putative alpha-motor neurons, neurons innervating principal dorsal muscles demonstrated higher content of CHT than neurons innervating limb muscles.
2.Ultrastructural localization at the synapse
To determine whether CHT is located at the presynaptic membrane or at the membrane of synaptic vesicles, we analyzed the localization of CHT at the monkey neuromuscular junction using post-embedding immunocytochemistry with electronmicroscopy. Although immunoreactivity was weaker than reported in the rat, most of the immunoreactivity for CHT was located inside the nerve terminal rather than on the presynaptic membrane. The findings are compatible with the CHT localization on the vesicular membrane reported in the rat, but for the exact localization at the vesicular membrane, further study will be necessary to determine the optimal condition that preserve both the immunoreactivity for CHT and the structure of vesicular membrane. These electron microscopic studies were performed in collaboration with Professor Seiji Matsuda at Ehime University. Less
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Research Products
(2 results)
