Evidence map›Paper›PMID 36571441›Full record

ReviewAmerican journal of physiology. Cell physiology2023

Improving physiological relevance of cell culture: the possibilities, considerations, and future directions of the ex vivo coculture model.

Sophie L Allen, Bradley T Elliott, Brian P Carson, Leigh Breen

Open access · hybridAbstract readReview
In one paragraph

Review in American journal of physiology. Cell physiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

15 citing papers in PubMed, 16 citations in OpenAlex.

  1. Trial
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  9. Autonomous cortisol secretion promotes vascular calcification in vivo and in vitro under hyperaldosteronism.Hypertension research : official journal of the Japanese Society of Hypertension · 2025
    Article
  10. Article
  11. Article
  12. 3D Culture Analysis of Cancer Cell Adherence toTissue engineering. Part C, Methods · 2024
    Article
  13. Article
  14. Translational pathology in drug discovery.Frontiers in pharmacology · 2024
    Article
  15. In Vitro Models of Amyotrophic Lateral Sclerosis.Cellular and molecular neurobiology · 2023
    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

4 authors at 3 institutions in 2 countries.

Sophie L AllenSchool of Sport Exercise and Rehabilitation Sciences, https://ror.org/03angcq70University of Birmingham, Birmingham, United Kingdom.ORCID 0000-0002-8349-9745
Bradley T ElliottTranslational Physiology Research Group, School of Life Sciences, University of Westminster, London, United Kingdom.
Brian P CarsonDepartment of Physical Education and Sport Sciences, Faculty of Education and Health Sciences, University of Limerick, Limerick, Ireland.ORCID 0000-0001-8350-1481
Leigh BreenSchool of Sport Exercise and Rehabilitation Sciences, https://ror.org/03angcq70University of Birmingham, Birmingham, United Kingdom.
University Hospitals Birmingham NHS Foundation Trust · GBUniversity of Limerick · IEUniversity of Westminster · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In vitro models provide an important platform for the investigation of cellular growth and atrophy to inform, or extend mechanistic insights from, logistically challenging in vivo trials. Although these models allow for the identification of candidate mechanistic pathways, many models involve supraphysiological dosages, nonphysiological conditions, or experimental changes relating to individual proteins or receptors, all of which limit translation to human trials. To overcome these drawbacks, the use of ex vivo human plasma and serum has been used in cellular models to investigate changes in myotube hypertrophy, cellular protein synthesis, anabolic and catabolic markers in response to differing age, disease states, and nutrient status. However, there are currently no concurrent guidelines outlining the optimal methodology for this model. This review discusses the key methodological considerations surrounding the use of ex vivo plasma and serum with a focus in application to skeletal muscle cell lines (i.e., C2C12, L6, and LHCN-M2) and human primary skeletal muscle cells (HSMCs) as a means to investigate molecular signaling in models of atrophy and hypertrophy, alongside future directions.

Indexed as

Cell Culture TechniquesMuscle Fibers, SkeletalAtrophyCell LineCoculture TechniquesHumansHypertrophyMuscle, SkeletalMuscular Atrophycell cultureex vivoin vitroplasmaserum

Identifiers

PMID36571441
PMCPMC9902212
OpenAlexW4312195924

What OpenQuestion 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 OpenQuestion graph.