Evidence map›Paper›PMID 20125125›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2010

In vivo fluorescence imaging of muscle cell regeneration by transplanted EGFP-labeled myoblasts.

Xiaoyin Xu, Zhong Yang, Qiang Liu, Yaming Wang

Open access · bronzeAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

14 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. An image processing approach to analyze morphological features of microscopic images of muscle fibers.Computerized medical imaging and graphics : the official journal of the Computerized Medical Imaging Society · 2014
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. 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

4 authors at 3 institutions in 1 country.

Xiaoyin XuFunctional and Molecular Imaging Center, Optical Imaging Laboratory, Department of Radiology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Zhong Yang
Qiang Liu
Yaming Wang
Harvard University · USHarvard Stem Cell Institute · USImaging Center · US

Funding

Strategies to improve stem cell engraftment into muscleK02AR051181 · NIAMS · BRIGHAM AND WOMEN'S HOSPITAL · PI WANG, YAMING · 2004 to 2008
$535k
NIAMS NIH HHS 5K02AR051181NIAMS NIH HHS K02 AR051181
6 · The paper itself

Abstract

In vivo fluorescence imaging (FLI) enables monitoring fluorescent protein (FP)-labeled cells and proteins in living organisms noninvasively. Here, we examined whether this modality could reach a sufficient sensitivity to allow evaluation of the regeneration process of enhanced green fluorescent protein (eGFP)-labeled muscle precursors (myoblasts). Using a basic FLI station, we were able to detect clear fluorescence signals generated by 40,000 labeled cells injected into a tibialis anterior (TA) muscle of mouse. We observed that the signal declined to approximately 25% on the 48 hours of cell injection followed by a recovery starting at the second day and reached a peak of approximately 45% of the original signal by the 7th day, suggesting that the survived population underwent a limited run of proliferation before differentiation. To assess whether transplanted myoblasts could form satellite cells, we injured the transplanted muscles repeatedly with cardiotoxin. We observed a recovery of fluorescence signal following a disappearance of the signal after each cardiotoxin injection. Histology results showed donor-derived cells located underneath basal membrane and expressing Pax7, confirming that the regeneration observed by imaging was indeed mediated by donor-derived satellite cells. Our results show that FLI is a powerful tool that can extend our ability to unveil complicated biological processes such as stem cell-mediated regeneration.

Indexed as

RegenerationAnimalsCardiotoxinsCell DifferentiationCell ProliferationGreen Fluorescent ProteinsMiceMice, Inbred C57BLMice, SCIDMicroscopy, FluorescenceMuscle, SkeletalMyoblastsPAX7 Transcription FactorSatellite Cells, Skeletal MuscleCardiotoxinsenhanced green fluorescent proteinGreen Fluorescent ProteinsPAX7 protein, humanPAX7 Transcription Factor

Identifiers

PMID20125125
PMCPMC2862520
OpenAlexW2085768352

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.