Evidence map›Paper›PMID 34212303›Full record

ReviewStem cell reviews and reports2022

Current Progress in the Creation, Characterization, and Application of Human Stem Cell-derived in Vitro Neuromuscular Junction Models.

Eileen Lynch, Emma Peek, Megan Reilly, Claire FitzGibbons, Samantha Robertson, Masatoshi Suzuki

Open access · greenAbstract readReview
In one paragraph

Review in Stem cell reviews and reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

8 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Aberrant evoked calcium signaling and nAChR cluster morphology in aFrontiers in cell and developmental biology · 2024
    Article
  4. Article
  5. Optimization of Application-Driven Development ofTissue engineering. Part B, Reviews · 2022
    Review
  6. Article
  7. Review
  8. 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

6 authors at 2 institutions in 1 country.

Eileen LynchDepartment of Comparative Biosciences, University of Wisconsin-Madison, Madison, WI, USA.
Emma PeekDepartment of Comparative Biosciences, University of Wisconsin-Madison, Madison, WI, USA.
Megan ReillyDepartment of Comparative Biosciences, University of Wisconsin-Madison, Madison, WI, USA.
Claire FitzGibbonsDepartment of Comparative Biosciences, University of Wisconsin-Madison, Madison, WI, USA.
Samantha RobertsonDepartment of Comparative Biosciences, University of Wisconsin-Madison, Madison, WI, USA.
Masatoshi SuzukiDepartment of Comparative Biosciences, University of Wisconsin-Madison, Madison, WI, USA. masatoshi.suzuki@wisc.edu.ORCID 0000-0003-3253-0711
University of Wisconsin–Madison · USUniversity of Wisconsin System · US

Funding

Stem cell-based tissue engineering for myotendinous junction modeling and repairR01AR077191 · NIAMS · UNIVERSITY OF WISCONSIN-MADISON · PI SUZUKI, MASATOSHI · 2020 to 2024
$1.7M
Muscle stem cells: New ALS growth factor therapy and disease modelR01NS091540 · NINDS · UNIVERSITY OF WISCONSIN-MADISON · PI SUZUKI, MASATOSHI · 2015 to 2019
$1.7M
NIAMS NIH HHS R01 AR077191NINDS NIH HHS R01 NS091540
6 · The paper itself

Abstract

Human pluripotent stem cells (PSCs) such as embryonic stem cells (ESCs) or induced pluripotent stem cells (iPSCs) are of great value for studying developmental processes, disease modeling, and drug testing. One area in which the use of human PSCs has become of great interest in recent years is for in vitro models of the neuromuscular junction (NMJ). The NMJ is a synapse at which a motor neuron releases acetylcholine to bind to skeletal muscle and stimulate contraction. Degeneration of the NMJ and subsequent loss of muscle function is a common feature of many neuromuscular diseases such as myasthenia gravis, spinal muscular atrophy, and amyotrophic lateral sclerosis. In order to develop new therapies for patients with neuromuscular diseases, it is essential to understand mechanisms taking place at the NMJ. However, we have limited ability to study the NMJ in living human patients, and animal models are limited by physiological relevance. Therefore, an in vitro model of the NMJ consisting of human cells is of great value. The use of stem cells for in vitro NMJ models is still in progress and requires further optimization in order to yield reliable, reproducible results. The objective of this review is (1) to outline the current progress towards fully PSC-derived in vitro co-culture models of the human NMJ and (2) to discuss future directions and challenges that must be overcome in order to create reproducible fully PSC-derived models that can be used for developmental studies, disease modeling, and drug testing.

Indexed as

Amyotrophic Lateral SclerosisInduced Pluripotent Stem CellsMuscular Atrophy, SpinalAnimalsHumansMotor NeuronsNeuromuscular JunctionCo-cultureDevelopmentDisease modelingDrug testingNeuromuscular junctionPluripotent stem cells

Identifiers

PMID34212303
PMCPMC8720113
OpenAlexW3174514934

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.