Evidence map›Paper›PMID 35396689›Full record

ArticleCellular and molecular life sciences : CMLS2022

Novel integrated workflow allows production and in-depth quality assessment of multifactorial reprogrammed skeletal muscle cells from human stem cells.

Dinis Faustino, Heinrich Brinkmeier, Stella Logotheti, Anika Jonitz-Heincke, Hande Yilmaz, Isil Takan, Kirsten Peters, Rainer Bader, Hermann Lang, Athanasia Pavlopoulou and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 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
0.6field-weighted citation impact, top 37% 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. Review
  2. Article
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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

12 authors at 3 institutions in 2 countries.

Dinis FaustinoInstitute of Experimental Gene Therapy and Cancer Research, Rostock University Medical Center, 18057, Rostock, Germany.
Heinrich BrinkmeierInstitute of Pathophysiology, University Medicine Greifswald, 17489, Greifswald, Germany.
Stella LogothetiInstitute of Experimental Gene Therapy and Cancer Research, Rostock University Medical Center, 18057, Rostock, Germany.
Anika Jonitz-HeinckeBiomechanics and Implant Technology Research Laboratory, Department of Orthopedics, Rostock University Medical Centre, 18057, Rostock, Germany.
Hande YilmazInstitute of Experimental Gene Therapy and Cancer Research, Rostock University Medical Center, 18057, Rostock, Germany.
Isil TakanIzmir Biomedicine and Genome Center (IBG), Balcova, 35340, Izmir, Turkey.
Kirsten PetersDepartment of Cell Biology, Rostock University Medical Center, 18057, Rostock, Germany.
Rainer BaderBiomechanics and Implant Technology Research Laboratory, Department of Orthopedics, Rostock University Medical Centre, 18057, Rostock, Germany.
Hermann LangDepartment of Operative Dentistry and Periodontology, Rostock University Medical Centre, 18057, Rostock, Germany.
Athanasia PavlopoulouIzmir Biomedicine and Genome Center (IBG), Balcova, 35340, Izmir, Turkey.
Brigitte M Pützer *Institute of Experimental Gene Therapy and Cancer Research, Rostock University Medical Center, 18057, Rostock, Germany. brigitte.puetzer@med.uni-rostock.de.ORCID http://orcid.org/0000-0003-1351-082X
Alf Spitschak *Institute of Experimental Gene Therapy and Cancer Research, Rostock University Medical Center, 18057, Rostock, Germany.
University of Rostock · DEDokuz Eylül University · TRUniversitätsmedizin Greifswald · DE

Funding

Deutsche Forschungsgemeinschaft PU 188/19-1European Union Structural Fund ESF-14BM-A55-0025-18-A02European Union Structural Fund ESF/14-BM-A55-0026/18
6 · The paper itself

Abstract

Skeletal muscle tissue engineering aims at generating biological substitutes that restore, maintain or improve normal muscle function; however, the quality of cells produced by current protocols remains insufficient. Here, we developed a multifactor-based protocol that combines adenovector (AdV)-mediated MYOD expression, small molecule inhibitor and growth factor treatment, and electrical pulse stimulation (EPS) to efficiently reprogram different types of human-derived multipotent stem cells into physiologically functional skeletal muscle cells (SMCs). The protocol was complemented through a novel in silico workflow that allows for in-depth estimation and potentially optimization of the quality of generated muscle tissue, based on the transcriptomes of transdifferentiated cells. We additionally patch-clamped phenotypic SMCs to associate their bioelectrical characteristics with their transcriptome reprogramming. Overall, we set up a comprehensive and dynamic approach at the nexus of viral vector-based technology, bioinformatics, and electrophysiology that facilitates production of high-quality skeletal muscle cells and can guide iterative cycles to improve myo-differentiation protocols.

Indexed as

Muscle DevelopmentMuscle Fibers, SkeletalCell DifferentiationHumansMuscle, SkeletalMyoD ProteinStem CellsWorkflowMyoD ProteinAdenovector-mediated MYOD expressionElectrical pulse stimulationMultipotent stem cellsMyogenic differentiationMyo-informaticsSkeletal muscle transcriptomicsSmall molecules

Identifiers

PMID35396689
PMCPMC8993739
OpenAlexW4223567661

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.