Evidence map›Paper›PMID 34781416›Full record

ArticleJournal of tissue engineering and regenerative medicine2022

Tissue engineered skeletal muscle model of rheumatoid arthritis using human primary skeletal muscle cells.

Catherine E Oliver, Hailee Patel, James Hong, Jonathan Carter, William E Kraus, Kim M Huffman, George A Truskey

Open access · greenAbstract read
In one paragraph

Article in Journal of tissue engineering and regenerative medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.3field-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

12 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Emerging Landscape ofACS pharmacology & translational science · 2024
    Review
  9. Article
  10. Article
  11. Review
  12. 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

7 authors at 1 institution in 1 country.

Catherine E OliverDepartment of Biomedical Engineering, Duke University, Durham, North Carolina, USA.ORCID 0000-0003-3040-1326
Hailee PatelDepartment of Biomedical Engineering, Duke University, Durham, North Carolina, USA.
James HongDepartment of Biomedical Engineering, Duke University, Durham, North Carolina, USA.ORCID 0000-0003-3452-8607
Jonathan CarterDepartment of Biomedical Engineering, Duke University, Durham, North Carolina, USA.
William E KrausDepartment of Medicine, Duke University School of Medicine, Durham, North Carolina, USA.
Kim M HuffmanDepartment of Medicine, Duke University School of Medicine, Durham, North Carolina, USA.
George A TruskeyDepartment of Biomedical Engineering, Duke University, Durham, North Carolina, USA.
Duke University · US

Funding

Vascular, Cardiac, and Lung Alveolar Human Microphysiological Systems for SARS-CoV-2 Drug ScreeningUH3TR002142 · NCATS · DUKE UNIVERSITY · PI TRUSKEY, GEORGE A · 2019 to 2021
$4.0M
Developing An In Vitro Human Myobundle Model Of Rheumatoid ArthritisR21AR072283 · NIAMS · DUKE UNIVERSITY · PI TRUSKEY, GEORGE A · 2017 to 2018
$373k
NCATS NIH HHS UH3 TR002142NIAMS NIH HHS R21 AR072283NIH HHS AR072283NIH HHS UH3TR002142
6 · The paper itself

Abstract

Rheumatoid arthritis (RA) is a chronic inflammatory disease primarily targeting the joints. Autoreactive immune cells involved in RA affect other tissues, including skeletal muscle. Patients with RA experience diminished physical function, limited mobility, reduced muscle function, chronic pain, and increased mortality. To explore the impact of RA on skeletal muscle, we engineered electrically responsive, contractile human skeletal muscle constructs (myobundles) using primary skeletal muscle cells isolated from the vastus lateralis muscle of 11 RA patients (aged 57-74) and 10 aged healthy donors (aged 55-76), as well as from the hamstring muscle of six young healthy donors (less than 18 years of age) as a benchmark. Since all patients were receiving treatment for the disease, RA disease activity was mild. In 2D culture, RA myoblast purity, growth rate, and senescence were not statistically different than aged controls; however, RA myoblast purity showed greater variance compared to controls. Surprisingly, in 3D culture, contractile force production by RA myobundles was greater compared to aged controls. In support of this finding, assessment of RA myofiber maturation showed increased area of sarcomeric α-actinin (SAA) expression over time compared to aged controls. Furthermore, a linear regression test indicated a positive correlation between SAA protein levels and tetanus force production in RA and controls. Our findings suggest that medications prescribed to RA patients may maintain-or even enhance-muscle function, and this effect is retained and observed in in vitro culture. Future studies regarding the effects of RA therapeutics on RA skeletal muscle, in vivo and in vitro, are warranted.

Indexed as

Arthritis, RheumatoidMuscle, SkeletalAgedHumansMiddle AgedMuscle ContractionMuscle Fibers, SkeletalMyoblastshuman skeletal muscleinflammationrheumatoid arthritistissue engineering

Identifiers

PMID34781416
PMCPMC9487182
OpenAlexW3211403542

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.