4.3 Article

Immunoreactivity of a G protein-coupled L-DOPA receptor GPR143, in Lewy bodies

期刊

NEUROSCIENCE RESEARCH
卷 148, 期 -, 页码 49-53

出版社

ELSEVIER IRELAND LTD
DOI: 10.1016/j.neures.2018.12.004

关键词

L-DOPA; Parkinson's disease; GPR143; Lewy; Bodies; alpha-Synuclein

资金

  1. Ministry of Education, Culture, Sport, Science and Technology (MEXT) of Japan [15H04687, 18H02580, 15K21273, 15K21271]
  2. Japanese SRF Grand for Biomedical Research [1565]
  3. Uehara Memorial Foundation [201320161, 201720339]
  4. fund for Creation of InnovationCenters for Advanced Interdisciplinary Research Areas Program inthe Project for Developing Innovation Systems from MEXT [42890001]
  5. Grants-in-Aid for Scientific Research [15K21273, 15K21271, 18H02580, 15H04687] Funding Source: KAKEN

向作者/读者索取更多资源

L-3,4-Dihydroxyphenylalanine (L-DOPA) has been believed to be an inert amino acid precursor of dopamine, and is the most effective therapeutic agent in Parkinson's disease (PD). We proposed L-DOPA as a neurotransmitter in the central nervous system. Recently, the ocular albinism 1 gene product, OA1/GPR143 (GPR143), was identified as a receptor for L-DOPA. In this study, we examined by generating anti-human GPR143 antibody, the localization of GPR143-immunoreactive signals in the brains from control and PD subjects. GPR143-immunoreactive signals were detected throughout the entire midbrain including substantia nigra pars compacta. In the PD brains, we found that GPR143-immunoreactive signals were detected in Lewy bodies and were colocalized with immunoreactive signals with anti-human Ser129 phosphorylated alpha-synuclein antibody. Although the significance of its occurrence in the inclusion bodies is unknown, our finding suggests possible implications of GPR143 in PD. (C) 2019 Elsevier B.V. and Japan Neuroscience Society. All rights reserved.

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