Immunohistochemical and in situ hybridization studies of choline acetyltransferase in large motor neurons of the human spinal cord

Y. Muroishi, S. Kasashima, I. Nakanishi and Y. Oda

First Department of Pathology, Faculty of Medicine, Kanazawa University, Kanazawa, Japan

Offprint requests to: Yoshio Oda, MD, First Department of Pathology, Faculty of Medicine, Kanazawa University, 13-1 Takara-machhi, Kanazawa, Ishikawa 920-8640, Japan. Fax: +81-76-265-2192. e-mail: yoda@med.kanazawa-u.ac.jp

Summary. The localization of choline acetyltransferase (ChAT) protein and mRNA was investigated in large motor neurons of the lumbar spinal cord of 10 autopsied individuals without neurological diseases, by immunohistochemistry and in situ hybridization. In the immunohistochemistry using 20 serial tissue sections with a total thickness of 80 µm, about 58~85% (average 67%) of the large motor neurons (30 µm and more in somal minimal diameter) in the ventral horn were stained with the anti-human ChAT antibody. In the positive neurons, most immunoreactive products were observed focally in the perikarya. Occasionally, the perikarya of some neurons were stained diffusely. In situ hybridization with a single 4 µm-thick tissue section showed that almost all large motor neurons had positive signals (93~100%, average 98%), which were distributed diffusely in the perikarya. The positivity rate in the in situ hybridization was higher than that in the immunohistochemistry for all 10 cases. These results indicate that ChAT mRNA is transcribed in almost all large motor neurons in the ventral horn of the human spinal cord, but ChAT protein cannot always be detected in the cytoplasm by immunohistochemistry. Histol. Histopathol. 15, 689-696 (2000)

Key words: Choline acetyltransferase, Spinal cord, Motor neuron, Human

DOI: 10.14670/HH-15.689