Evidence map›Paper›PMID 26040897›Full record

ArticleAmerican journal of physiology. Cell physiology2015

PEDF-derived peptide promotes skeletal muscle regeneration through its mitogenic effect on muscle progenitor cells.

Tsung-Chuan Ho, Yi-Pin Chiang, Chih-Kuang Chuang, Show-Li Chen, Jui-Wen Hsieh, Yu-Wen Lan, Yeou-Ping Tsao

Abstract read
In one paragraph

Article in American journal of physiology. Cell physiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

22 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Potential Therapeutic Strategies for Skeletal Muscle Atrophy.Antioxidants (Basel, Switzerland) · 2022
    Review
  6. Article
  7. 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 3 institutions in 1 country.

Tsung-Chuan HoDepartment of Medical Research, Mackay Memorial Hospital, Taipei, Taiwan;
Yi-Pin ChiangDepartment of Rehabilitation Medicine, Mackay Memorial Hospital, Taipei, Taiwan;
Chih-Kuang ChuangDepartment of Medical Research, Mackay Memorial Hospital, Taipei, Taiwan; Institute of Biotechnology, National Taipei University of Technology, Taipei, Taiwan; College of Medicine, Fu-Jen Catholic University, Taipei, Taiwan;
Show-Li ChenDepartment of Microbiology, School of Medicine, National Taiwan University, Taipei, Taiwan; and.
Jui-Wen HsiehDepartment of Ophthalmology, Mackay Memorial Hospital, Taipei, Taiwan; Department of Medicine, Nursing and Management College, Taipei, Taiwan.
Yu-Wen LanDepartment of Ophthalmology, Mackay Memorial Hospital, Taipei, Taiwan; Department of Medicine, Nursing and Management College, Taipei, Taiwan.
Yeou-Ping TsaoDepartment of Medical Research, Mackay Memorial Hospital, Taipei, Taiwan; Department of Ophthalmology, Mackay Memorial Hospital, Taipei, Taiwan; yptsao@yahoo.com.
Mackay Memorial Hospital · TWNational Taipei University of Technology · TWNational Taiwan University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In response injury, intrinsic repair mechanisms are activated in skeletal muscle to replace the damaged muscle fibers with new muscle fibers. The regeneration process starts with the proliferation of satellite cells to give rise to myoblasts, which subsequently differentiate terminally into myofibers. Here, we investigated the promotion effect of pigment epithelial-derived factor (PEDF) on muscle regeneration. We report that PEDF and a synthetic PEDF-derived short peptide (PSP; residues Ser(93)-Leu(112)) induce satellite cell proliferation in vitro and promote muscle regeneration in vivo. Extensively, soleus muscle necrosis was induced in rats by bupivacaine, and an injectable alginate gel was used to release the PSP in the injured muscle. PSP delivery was found to stimulate satellite cell proliferation in damaged muscle and enhance the growth of regenerating myofibers, with complete regeneration of normal muscle mass by 2 wk. In cell culture, PEDF/PSP stimulated C2C12 myoblast proliferation, together with a rise in cyclin D1 expression. PEDF induced the phosphorylation of ERK1/2, Akt, and STAT3 in C2C12 myoblasts. Blocking the activity of ERK, Akt, or STAT3 with pharmacological inhibitors attenuated the effects of PEDF/PSP on the induction of C2C12 cell proliferation and cyclin D1 expression. Moreover, 5-bromo-2'-deoxyuridine pulse-labeling demonstrated that PEDF/PSP stimulated primary rat satellite cell proliferation in myofibers in vitro. In summary, we report for the first time that PSP is capable of promoting the regeneration of skeletal muscle. The signaling mechanism involves the ERK, AKT, and STAT3 pathways. These results show the potential utility of this PEDF peptide for muscle regeneration.

Indexed as

AnimalsCell LineCell ProliferationEye ProteinsMaleMiceMuscle, SkeletalMyoblastsNerve Growth FactorsPigment Epithelium-Derived FactorRatsRats, Sprague-DawleyRegenerationSerpinsStem CellsEye ProteinsNerve Growth FactorsPigment Epithelium-Derived FactorSerpinsmyoblastpigment epithelial-derived factorsatellite cell

Identifiers

PMID26040897
PMCPMC4525084
OpenAlexW2096529052

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.