Evidence map›Paper›PMID 36792780›Full record

ReviewNature protocols2023

3D human induced pluripotent stem cell-derived bioengineered skeletal muscles for tissue, disease and therapy modeling.

Luca Pinton, Moustafa Khedr, Valentina M Lionello, Shilpita Sarcar, Sara M Maffioletti, Sumitava Dastidar, Elisa Negroni, SungWoo Choi, Noreen Khokhar, Anne Bigot and 4 more

Open access · hybridAbstract readReview
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In one paragraph

Review in Nature protocols, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
15.6field-weighted citation impact, top 1% 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

40 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
  2. Article
  3. Functionalized Biomimetic Scaffolds for Human-Derived Auditory Neural Circuit Construction.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  4. CRISPR-Cas9-mediated upregulation of utrophin ameliorates Duchenne muscular dystrophy.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
    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

14 authors at 6 institutions in 3 countries.

Luca Pinton *Department of Cell and Developmental Biology, University College London, London, UK.
Moustafa Khedr *Department of Cell and Developmental Biology, University College London, London, UK.
Valentina M LionelloDepartment of Cell and Developmental Biology, University College London, London, UK.
Shilpita SarcarDepartment of Cell and Developmental Biology, University College London, London, UK.
Sara M MaffiolettiDepartment of Cell and Developmental Biology, University College London, London, UK.
Sumitava DastidarDepartment of Cell and Developmental Biology, University College London, London, UK.
Elisa NegroniDepartment of Cell and Developmental Biology, University College London, London, UK.
SungWoo ChoiDepartment of Cell and Developmental Biology, University College London, London, UK.
Noreen KhokharDepartment of Cell and Developmental Biology, University College London, London, UK.
Anne BigotCenter for Research in Myology UMRS974, Sorbonne Université, INSERM, Myology Institute AIM, Paris, France.
John R CounsellUCL Division of Surgery and Interventional Science, Royal Free Hospital, London, UK.ORCID 0000-0001-9208-101X
Andreia Sofia BernardoThe Francis Crick Institute, London, UK.ORCID 0000-0002-5355-6657
Peter S ZammitRandall Centre for Cell and Molecular Biophysics, King's College London, London, UK.ORCID 0000-0001-9562-3072
Francesco Saverio TedescoDepartment of Cell and Developmental Biology, University College London, London, UK. f.s.tedesco@ucl.ac.uk.ORCID 0000-0001-5321-7682
The Francis Crick Institute · GBKing's College London · GBGreat Ormond Street Hospital · GBInserm · FRThe San Raffaele Telethon Institute for Gene Therapy · ITUniversity College London · GB

Funding

Biotechnology and Biological Sciences Research Council BB/M009513/1British Heart Foundation FS/12/37/29516Cancer Research UKDepartment of Health CL-2018-18-008European Research Council 759108Medical Research Council MC_PC_19038Medical Research Council MR/J006785/1Medical Research Council MR/P023215/1Medical Research Council MR/S002472/1Telethon 21687 and 23782Wellcome Trust 210987/Z/18/ZWellcome Trust CC0102Wellcome Trust FC001002
6 · The paper itself

Abstract

Skeletal muscle is a complex tissue composed of multinucleated myofibers responsible for force generation that are supported by multiple cell types. Many severe and lethal disorders affect skeletal muscle; therefore, engineering models to reproduce such cellular complexity and function are instrumental for investigating muscle pathophysiology and developing therapies. Here, we detail the modular 3D bioengineering of multilineage skeletal muscles from human induced pluripotent stem cells, which are first differentiated into myogenic, neural and vascular progenitor cells and then combined within 3D hydrogels under tension to generate an aligned myofiber scaffold containing vascular networks and motor neurons. 3D bioengineered muscles recapitulate morphological and functional features of human skeletal muscle, including establishment of a pool of cells expressing muscle stem cell markers. Importantly, bioengineered muscles provide a high-fidelity platform to study muscle pathology, such as emergence of dysmorphic nuclei in muscular dystrophies caused by mutant lamins. The protocol is easy to follow for operators with cell culture experience and takes between 9 and 30 d, depending on the number of cell lineages in the construct. We also provide examples of applications of this advanced platform for testing gene and cell therapies in vitro, as well as for in vivo studies, providing proof of principle of its potential as a tool to develop next-generation neuromuscular or musculoskeletal therapies.

Indexed as

Induced Pluripotent Stem CellsSatellite Cells, Skeletal MuscleCell DifferentiationCell LineageHumansMuscle, Skeletal

Identifiers

PMID36792780
OpenAlexW4320913118

What OpenQuestion holds

Textmetadata
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.