Evidence map›Paper›PMID 23438194›Full record

ArticleCellular reprogramming2013

Direct reprogramming of fibroblasts to myocytes via bacterial injection of MyoD protein.

Candace Bichsel, Dennis Neeld, Takashi Hamazaki, Lung-Ji Chang, Li-Jun Yang, Naohiro Terada, Shouguang Jin

Open access · greenAbstract read
In one paragraph

Article in Cellular reprogramming, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

26 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
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  9. Cellular reprogramming: Mathematics meets medicine.Wiley interdisciplinary reviews. Systems biology and medicine · 2020
    Review
  10. Article
  11. Review
  12. Article
  13. Bioreactor model of neuromuscular junction with electrical stimulation for pharmacological potency testing.Integrative biology : quantitative biosciences from nano to macro · 2017
    Article
  14. Review
  15. Article
  16. Highly efficient delivery of functional cargoes by the synergistic effect of GAG binding motifs and cell-penetrating peptides.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  17. Article
  18. Review
  19. 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

7 authors at 2 institutions in 1 country.

Candace BichselDepartment of Molecular Genetics and Microbiology, College of Medicine, University of Florida, Gainesville, FL 32610, USA.
Dennis Neeld
Takashi Hamazaki
Lung-Ji Chang
Li-Jun Yang
Naohiro Terada
Shouguang Jin
University of Florida · USFlorida College · US

Funding

iPSC Generation using Peptide Injection and Site-Selective HDAC InhibitionRC1GM091238 · NIGMS · UNIVERSITY OF FLORIDA · PI HAMAZAKI, TAKASHI, JIN, SHOUGUANG · 2009 to 2010
$965k
NIGMS NIH HHS RC1GM091238
6 · The paper itself

Abstract

Forced exogenous gene expression has been well characterized as an effective method for directing both cellular differentiation and dedifferentiation. However, transgene expression is not amenable for therapeutic application due to potential insertional mutagenesis. Protein-based techniques provide a safe alternative, but current protein delivery methods are quite limited by labor-intensive purification processes, low protein yield, and inefficient intracellular targeting. Such limitations may be overcome by using a naturally occurring bacterial protein injection system, called the type III secretion system (T3SS), which injects bacterial proteins directly into the eukaryotic cell cytoplasm. Using a genetically attenuated strain of Pseudomonas aeruginosa, we have previously described the ability of this system to easily deliver a high quantity of protein to both differentiated and pluripotent cells. MyoD is a key muscle regulatory factor, the overexpression of which is able to induce transdifferentiation of numerous cell types into functional myocytes. Here we demonstrate transient injection of MyoD protein by P. aeruginosa to be sufficient to induce myogenic conversion of mouse embryonic fibroblasts. In addition to clear morphological changes, muscle-specific gene expression has been observed both at mRNA and protein levels. These studies serve as a foundation for the bacterial delivery of transcription factors to efficiently modulate concentration-dependent and temporal activation of gene expression that directs cell fate without jeopardizing genomic integrity.

Indexed as

Cell TransdifferentiationAnimalsBacterial Secretion SystemsCell LineFibroblastsHumansMiceMuscle CellsMyoD ProteinPseudomonas aeruginosaPseudomonas InfectionsTransduction, GeneticBacterial Secretion SystemsMyoD1 myogenic differentiation proteinMyoD Protein

Identifiers

PMID23438194
PMCPMC3616421
OpenAlexW1702489159

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.