Evidence map›Paper›PMID 40826134›Full record

ArticleActa neuropathologica communications2025

Evidence of a novel α-synuclein strain isolated from a Parkinson's disease with dementia patient sample.

Sara A M Holec, Jisoo Lee, Chase R Khedmatgozar, Marcelina J Wojewska, Abby Oehler, Glenda M Halliday, Steve M Gentleman, Amanda L Woerman

Abstract read
In one paragraph

Article in Acta neuropathologica communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Sara A M HolecDepartment of Microbiology, Immunology, and Pathology, Prion Research Center, Colorado State University, 300 West Lake Street, Fort Collins, CO, 80521, USA.
Jisoo LeeInstitute for Neurodegenerative Diseases, Weill Institute for Neurosciences, University of California, San Francisco, CA, USA.
Chase R KhedmatgozarDepartment of Microbiology, Immunology, and Pathology, Prion Research Center, Colorado State University, 300 West Lake Street, Fort Collins, CO, 80521, USA.
Marcelina J WojewskaDepartment of Brain Sciences, Imperial College London, London, UK.
Abby OehlerInstitute for Neurodegenerative Diseases, Weill Institute for Neurosciences, University of California, San Francisco, CA, USA.
Glenda M HallidayBrain and Mind Centre & Faculty of Medicine and Health School of Medical Sciences, University of Sydney, Sydney, Australia.
Steve M GentlemanDepartment of Brain Sciences, Imperial College London, London, UK.
Amanda L WoermanDepartment of Microbiology, Immunology, and Pathology, Prion Research Center, Colorado State University, 300 West Lake Street, Fort Collins, CO, 80521, USA. amanda.woerman@colostate.edu.

Funding

Research Education ComponentP30AG062421 · NIA · MASSACHUSETTS GENERAL HOSPITAL · PI Christine S Ritchie · 2019 to 2026
$36.5M
Effect of Agent and Host Factors on Alpha-Synuclein Strain PathogenesisR01NS121294 · NINDS · UNIVERSITY OF MASSACHUSETTS AMHERST · PI Amanda L. Woerman · 2022 to 2026
$2.9M
NIA NIH HHS P30 AG062421NINDS NIH HHS R01 NS121294NINDS NIH HHS R01NS121294
6 · The paper itself

Abstract

Multiple system atrophy (MSA) and the Lewy body diseases (LBDs) are caused by α-synuclein misfolding into distinct conformations, or strains, with unique biological properties. MSA patient samples readily transmit disease following intracranial (i.c.) inoculation into humanized mice, whereas LBD samples typically do not. Unexpectedly, we identified one LBD patient sample that, following i.c. inoculation, transmitted neurological disease to four out of six mice over an extended incubation period. In light of these unexpected results, we sought to identify the α-synuclein strain responsible for disease onset. Using immunohistochemistry, we identified both Lewy bodies and oligodendroglial inclusions with a glial cytoplasmic inclusion-like appearance in the substantia nigra of the patient sample. To determine if these glial inclusions were due to the presence of low titer MSA α-synuclein in the sample, we performed a secondary passage of two terminal mouse brains from the primary passage and found that the humanized mice developed disease with a shortened incubation period. Unexpectedly, using our panel of mutant α-syn140–YFP cells to analyze the primary and secondary passage samples showed that the strain isolated in the in vivo studies has unique biological properties compared to the MSA and LBD strains. These data suggest that the oligodendroglial pathology in the LBD patient sample was not caused by MSA co-pathology, and provide evidence for the isolation of a novel distinct α-synuclein strain.

Indexed as

alpha-SynucleinDementiaLewy Body DiseaseParkinson DiseaseAgedAnimalsBrainDisease Models, AnimalFemaleHumansLewy BodiesMaleMiceMice, TransgenicMiddle AgedMultiple System Atrophyalpha-SynucleinLewy body diseasesNeurodegenerative diseaseStrain interactionsSynucleinopathies

Identifiers

PMID40826134
PMCPMC12362927

What Socratic holds

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LicenceCC BY
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Registered trials

None linked

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 Socratic graph.