Evidence map›Paper›PMID 33926115›Full record

ReviewInternational journal of molecular sciences2021

Lymphoblastoid Cell Lines as Models to Study Mitochondrial Function in Neurological Disorders.

Sarah Jane Annesley, Paul Robert Fisher

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

14 citing papers in PubMed, 17 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Role of Mitochondrial Dynamics in Cocaine's Neurotoxicity.International journal of molecular sciences · 2022
    Review
  10. Article
  11. Cells · 2022
    Review
  12. Mitochondrial Bioenergetics in Different Pathophysiological Conditions.International journal of molecular sciences · 2021
    Article
  13. Review
  14. Article
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.

Sarah Jane AnnesleyDepartment of Physiology, Anatomy and Microbiology, La Trobe University, Bundoora, VIC 3086, Australia.ORCID 0000-0002-7604-3985
Paul Robert FisherDepartment of Physiology, Anatomy and Microbiology, La Trobe University, Bundoora, VIC 3086, Australia.ORCID 0000-0003-1884-6306
La Trobe University · AU

Funding

Michael J. Fox Foundation for Parkinson's Research 10862.01THE JUDITH JANE MASON & HAROLD STANNETT WILLIAMS MEMORIAL FOUNDATION MASONMECFS051 and MAS2018F00026
6 · The paper itself

Abstract

Neurological disorders, including neurodegenerative diseases, are collectively a major cause of death and disability worldwide. Whilst the underlying disease mechanisms remain elusive, altered mitochondrial function has been clearly implicated and is a key area of study in these disorders. Studying mitochondrial function in these disorders is difficult due to the inaccessibility of brain tissue, which is the key tissue affected in these diseases. To overcome this issue, numerous cell models have been used, each providing unique benefits and limitations. Here, we focussed on the use of lymphoblastoid cell lines (LCLs) to study mitochondrial function in neurological disorders. LCLs have long been used as tools for genomic analyses, but here we described their use in functional studies specifically in regard to mitochondrial function. These models have enabled characterisation of the underlying mitochondrial defect, identification of altered signalling pathways and proteins, differences in mitochondrial function between subsets of particular disorders and identification of biomarkers of the disease. The examples provided here suggest that these cells will be useful for development of diagnostic tests (which in most cases do not exist), identification of drug targets and testing of pharmacological agents, and are a worthwhile model for studying mitochondrial function in neurological disorders.

Indexed as

Amyotrophic Lateral SclerosisAtaxiaCell LineFatigue Syndrome, ChronicFragile X SyndromeHumansHuntington DiseaseLymphocytesMitochondriaModels, BiologicalNervous System DiseasesNeurodegenerative DiseasesOxidative StressParkinson DiseaseReactive Oxygen SpeciesTremorReactive Oxygen Speciescell modelslymphoblastoid cell linesmitochondrianeurodegenerative diseaseneurological disorder

Identifiers

PMID33926115
PMCPMC8123577
OpenAlexW3158908455

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.