Evidence map›Paper›PMID 19328199›Full record

ReviewExperimental neurology2009

The cybrid model of sporadic Parkinson's disease.

Patricia A Trimmer, James P Bennett

Abstract readReview
In one paragraph

Review in Experimental neurology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
5.2field-weighted citation impact, top 4% of its field
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

28 citing papers in PubMed, 53 citations in OpenAlex.

  1. Review
  2. Article
  3. Molecules (Basel, Switzerland) · 2021
    Article
  4. Article
  5. Review
  6. Cybrid Models of Pathological Cell Processes in Different Diseases.Oxidative medicine and cellular longevity · 2018
    Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. The Function of Autophagy in Neurodegenerative Diseases.International journal of molecular sciences · 2015
    Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Mitochondria in neurodegeneration.Advances in experimental medicine and biology · 2012
    Review
  19. Article
  20. Review
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

2 authors at 1 institution in 1 country.

Patricia A TrimmerMorris K. Udall Parkinson's Disease Research Center of Excellence, Department of Neurology, University of Virginia, Charlottesville, 22908, USA. pat5q@virginia.edu
James P Bennett
University of Virginia · US

Funding

Proteasomal Dysfunction and Protein Aggregation in PDP50NS039788 · NINDS · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI CAPALDI, RODERICK A · 1999 to 2009
$10.9M
MITOCHONDRIAL MOVEMENT IN CELLULAR MODELS OF ALZHEIMER'S AND PARKINSON'S DP01AG014373 · NIA · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI BENNETT, JAMES PEPPER · 1998 to 2000
$833k
NIA NIH HHS P01 AG014373NINDS NIH HHS P50 NS039788
6 · The paper itself

Abstract

Parkinson's disease (PD) is the eponym attached to the most prevalent neurodegenerative movement disorder of adults, derived from observations of an early nineteenth century physician and paleontologist, James Parkinson, and is now recognized to encompass much more than a movement disorder clinically or dopamine neuron death pathologically. Most PD ( approximately 90%) is sporadic (sPD), is associated with mitochondrial deficiencies and has been studied in cell and animal models arising from the use of mitochondrial toxins that unfortunately have not predicted clinical efficacy to slow disease progression in humans. We have extensively studied the cytoplasmic hybrid ("cybrid") model of sPD in which donor mtDNAs are introduced into and expressed in neural tumor cells with identical nuclear genetic and environmental backgrounds. sPD cybrids demonstrate many abnormalities in which increased oxidative stress drives downstream antioxidant response and cell death activating signaling pathways. sPD cybrids regulate mitochondrial ETC genes and gene ontology families like sPD brain. sPD cybrids spontaneously form Lewy bodies and Lewy neurites, linking mtDNA expression to neuropathology, and demonstrate impaired organelle transport in processes and reduced mitochondrial respiration. Our recent studies show that near-infrared laser light therapy normalizes mitochondrial movement and can stimulate respiration in sPD cybrid neurons, and mitochondrial gene therapy can restore respiration and stimulate mitochondrial ETC gene and protein expression. sPD cybrids have provided multiple lines of circumstantial evidence linking mtDNA to sPD pathogenesis and can serve as platforms for therapy development. sPD cybrid models can be improved by the use of non-tumor human stem cell-derived neural precursor cells and by an introduction of postmortem brain mtDNA to test its causality directly.

Indexed as

AnimalsCell DeathCell Line, TumorDNA, MitochondrialGene ExpressionHumansHybrid CellsNeuronsOxidative StressParkinson DiseaseSignal TransductionDNA, Mitochondrial

Identifiers

PMID19328199
PMCPMC2735256
OpenAlexW2061222846

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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 OpenQuestion graph.