Evidence map›Paper›PMID 36055608›Full record

ArticleActa biomaterialia2022

Matrix produced by diseased cardiac fibroblasts affects early myotube formation and function.

Janny Piñeiro-Llanes, Silveli Suzuki-Hatano, Ananya Jain, Valerie A Pérez Medina, William Todd Cade, Christina A Pacak, Chelsey S Simmons

Open access · greenAbstract read
In one paragraph

Article in Acta biomaterialia, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Barth Syndrome:Genes · 2025
    Review
  3. Article
  4. 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 4 institutions in 2 countries.

Janny Piñeiro-LlanesJ. Crayton Pruitt Family Department of Biomedical Engineering, Herbert Wertheim College of Engineering, University of Florida, Gainesville, FL 32611, USA.
Silveli Suzuki-HatanoDepartment of Pediatrics, University of Florida College of Medicine, Gainesville, FL 32610, USA.
Ananya JainJ. Crayton Pruitt Family Department of Biomedical Engineering, Herbert Wertheim College of Engineering, University of Florida, Gainesville, FL 32611, USA.
Valerie A Pérez MedinaDepartment of Mechanical Engineering, University of Puerto Rico, Mayaguez 00682, Puerto Rico.
William Todd CadePhysical Therapy Division, Duke University, 311 Trent Drive, Durham, NC 27710, USA.
Christina A PacakDepartment of Pediatrics, University of Florida College of Medicine, Gainesville, FL 32610, USA; Neurology Department, Medical School, University of Minnesota, WMBB 4-188 2101 6th Street SE, Minneapolis 55455, USA.
Chelsey S SimmonsJ. Crayton Pruitt Family Department of Biomedical Engineering, Herbert Wertheim College of Engineering, University of Florida, Gainesville, FL 32611, USA; Department of Mechanical and Aerospace Engineering Herbert Wertheim College of Engineering, University of Florida. Electronic address: css@ufl.edu.
University of Florida · USDuke University · USFlorida College · USUniversity of Puerto Rico-Mayaguez · PR

Funding

Mechanisms and Treatment of Cardiac and Skeletal Muscular Dysfunction in Barth SyndromeR01HL136759 · NHLBI · UNIVERSITY OF MINNESOTA · PI PACAK, CHRISTINA A. · 2018 to 2022
$2.2M
Acquisition of a Q Exactive HF Hybrid Quadrupole-OrbitrapS10OD021758 · OD · UNIVERSITY OF FLORIDA · PI BASSO, KARI B · 2017 to 2017
$600k
NHLBI NIH HHS R01 HL136759NIH HHS S10 OD021758
6 · The paper itself

Abstract

The extracellular matrix (ECM) provides both physical and chemical cues that dictate cell function and contribute to muscle maintenance. Muscle cells require efficient mitochondria to satisfy their high energy demand, however, the role the ECM plays in moderating mitochondrial function is not clear. We hypothesized that the ECM produced by stromal cells with mitochondrial dysfunction (Barth syndrome, BTHS) provides cues that contribute to metabolic dysfunction independent of muscle cell health. To test this, we harnessed the ECM production capabilities of human pluripotent stem-cell-derived cardiac fibroblasts (hPSC-CFs) from healthy and BTHS patients to fabricate cell-derived matrices (CDMs) with controlled topography, though we found that matrix composition from healthy versus diseased cells influenced myotube formation independent of alignment cues. To further investigate the effects of matrix composition, we then examined the influence of healthy- and BTHS-derived CDMs on myotube formation and metabolic function. We found that BTHS CDMs induced lower fusion index, lower ATP production, lower mitochondrial membrane potential, and higher ROS generation than the healthy CDMs. These findings imply that BTHS-derived ECM alone contributes to myocyte dysfunction in otherwise healthy cells. Finally, to investigate potential mechanisms, we defined the composition of CDMs produced by hPSC-CFs from healthy and BTHS patients using mass spectrometry and identified 15 ECM and related proteins that were differentially expressed in the BTHS-CDM compared to healthy CDM. Our results highlight that ECM composition affects skeletal muscle formation and metabolic efficiency in otherwise healthy cells, and our methods to generate patient-specific CDMs are a useful tool to investigate the influence of the ECM on disease progression and to investigate variability among diseased patients. STATEMENT OF SIGNIFICANCE: Muscle function requires both efficient metabolism to generate force and structured extracellular matrix (ECM) to transmit force, and we sought to examine the interactions between metabolism and ECM when metabolic disease is present. We fabricated patient-specific cell derived matrices (CDMs) with controlled topographic features to replicate the composition of healthy and mitochondrial-diseased (Barth syndrome) ECM. We found that disease-derived ECM negatively affects metabolic function of otherwise healthy myoblasts, and we identified several proteins in disease-derived ECM that may be mediating this dysfunction. We anticipate that our patient-specific CDM system could be fabricated with other topographies and cell types to study cell functions and diseases of interest beyond mitochondrial dysfunction and, eventually, be applied toward personalized medicine.

Indexed as

Barth SyndromeAdenosine TriphosphateExtracellular MatrixFibroblastsHumansMuscle Fibers, SkeletalReactive Oxygen SpeciesAdenosine TriphosphateReactive Oxygen SpeciesBarth syndromeCell-derived matricesExtracellular matrixMitochondriaMyogenesisTissue engineering

Identifiers

PMID36055608
PMCPMC10625442
OpenAlexW4293764055

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.