Evidence map›Paper›PMID 40372528›Full record

ArticleCellular and molecular life sciences : CMLS2025

GPI-anchorless prion disease is sensitive to oxidative stress and shows potential for treatment with edaravone, based on iPS-derived neuron study.

Kosuke Matsuzono, Hiroyuki Honda, Takafumi Mashiko, Reiji Koide, Eiji Sakashita, Hitoshi Endo, Tetsuyuki Kitamoto, Shigeru Fujimoto

Abstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Kosuke MatsuzonoDivision of Neurology, Department of Medicine, Jichi Medical University School of Medicine, Yakushiji 3311-1, Shimotsuke, Tochigi, 329-0498, Japan. kmatsuzono51@jichi.ac.jp.ORCID http://orcid.org/0000-0002-9455-3903
Hiroyuki HondaDepartment of Neuropathology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Takafumi MashikoDivision of Neurology, Department of Medicine, Jichi Medical University School of Medicine, Yakushiji 3311-1, Shimotsuke, Tochigi, 329-0498, Japan.
Reiji KoideDivision of Neurology, Department of Medicine, Jichi Medical University School of Medicine, Yakushiji 3311-1, Shimotsuke, Tochigi, 329-0498, Japan.
Eiji SakashitaDepartment of Biochemistry, Jichi Medical University, Tochigi, Japan.
Hitoshi EndoDepartment of Biochemistry, Jichi Medical University, Tochigi, Japan.
Tetsuyuki KitamotoDivision of CJD Science and Technology, Department of Neurological Science, Tohoku University Graduate School of Medicine, Miyagi, Japan.
Shigeru FujimotoDivision of Neurology, Department of Medicine, Jichi Medical University School of Medicine, Yakushiji 3311-1, Shimotsuke, Tochigi, 329-0498, Japan.

Funding

Ministry of Education, Science, Culture, and Sports of Japan 21K15231YOKOYAMA Foundation for Clinical Pharmacology YRY-2002
6 · The paper itself

Abstract

Only a few reports have generated induced pluripotent stem cells from patients with prion diseases, making it important to conduct translational studies using cells derived from individuals with prion protein (PRNP) mutations. In this study, we established induced pluripotent stem cells from a patient with a glycosylphosphatidylinositol-anchorless PRNP mutation (Y162X), which leads to abnormal deposits of prion protein in various organs. While no abnormal intracellular prion protein deposits were observed in the neurons differentiated from PRNP Y162X induced pluripotent stem cells, extracellular PrP aggregates secretions were significantly increased, and these cells were significantly more sensitive to oxidative stress compared to control cells. Utilizing this PRNP Y162X iPSC-derived neuron model, we discovered that edaravone reduced the sensitivity of PRNP Y162X cells to oxidative stress. Following this finding, we treated a PRNP Y162X patient with edaravone for two years, which successfully suppressed indicators of disease progression. Our study demonstrates that the pathology of the glycosylphosphatidylinositol-anchorless PRNP mutation is associated with oxidative stress and highlights the potential of induced pluripotent stem cell technology in identifying novel treatments for rare prion diseases.

Indexed as

EdaravoneInduced Pluripotent Stem CellsNeuronsOxidative StressPrion DiseasesPrion ProteinsCell DifferentiationGlycosylphosphatidylinositolsHumansMutationEdaravoneGlycosylphosphatidylinositolsPrion ProteinsPRNP protein, humanEdaravoneGPI anchoriPSCsOxidative stressPrion

Identifiers

PMID40372528
PMCPMC12081781

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.