4.2 Article

Isopentenyl diphosphate isomerase, a cholesterol synthesizing enzyme, is localized in Lewy bodies

期刊

NEUROPATHOLOGY
卷 35, 期 5, 页码 432-440

出版社

WILEY-BLACKWELL
DOI: 10.1111/neup.12204

关键词

alpha-synuclein; cholesterol; isopentenyl diphosphate isomerase; Lewy body; Parkinson's disease

资金

  1. JSPS [26430049, 26430050, 26860655, 24300131]
  2. Brain Research Institute, Niigata University [2014-2508]
  3. Research Committee for Ataxic Disease from the Ministry of Health, Labor and Welfare, Japan
  4. NCNP [24-5]
  5. Grants-in-Aid for Scientific Research [26430049, 26430050, 26860655] Funding Source: KAKEN

向作者/读者索取更多资源

Isopentenyl diphosphate isomerase (IDI) is a cytoplasmic enzyme involved in the biosynthesis of isoprenoids including cholesterols. IDI has two isoforms in humans: IDI1 and IDI2. Since lipids are known to be a component of Lewy bodies (LBs), we investigated the immunohistochemical localization of IDI1 and IDI2 in the brain of patients with LB disease and multiple system atrophy (MSA) and normal control subjects. In normal controls, the cytoplasm of neurons was weakly immunostained with anti-IDI1 and anti-IDI2 antibodies throughout the nervous system. In LB disease, brainstem-type LBs were strongly positive for IDI1 and IDI2, and cortical LBs were unstained or barely immunolabeled. Double immunofluorescence staining revealed co-localization of phosphorylated -synuclein with IDI1 or IDI2. Glial cytoplasmic inclusions in MSA were unstained. Previous studies have shown that levels of cholesterol metabolites are increased in the cerebral cortex of patients with LB disease, and that these metabolites accelerate -synuclein aggregation. The present findings suggest that IDI1 and IDI2 may be associated with the production of cholesterol metabolites in neurons, leading to -synuclein aggregation during the process of LB formation.

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