Evidence map›Paper›PMID 33023189›Full record

ArticleCells2020

ProNGF/p75NTR Axis Drives Fiber Type Specification by Inducing the Fast-Glycolytic Phenotype in Mouse Skeletal Muscle Cells.

Valentina Pallottini, Mayra Colardo, Claudia Tonini, Noemi Martella, Georgios Strimpakos, Barbara Colella, Paola Tirassa, Sabrina Di Bartolomeo, Marco Segatto

Open access · goldAbstract read
In one paragraph

Article in Cells, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

13 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
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  5. Review
  6. Article
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  11. Cell Surface Proteins for Enrichment andStem cells international · 2022
    Article
  12. Biological Aspects of Selected Myokines in Skeletal Muscle: Focus on Aging.International journal of molecular sciences · 2021
    Review
  13. 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

9 authors at 3 institutions in 1 country.

Valentina PallottiniDepartment of Science, University of Rome "Roma Tre", 00146 Rome, Italy.ORCID 0000-0003-2511-6168
Mayra ColardoDepartment of Biosciences and Territory, University of Molise, 86090 Pesche (IS), Italy.
Claudia ToniniDepartment of Science, University of Rome "Roma Tre", 00146 Rome, Italy.ORCID 0000-0002-9979-1142
Noemi MartellaDepartment of Biosciences and Territory, University of Molise, 86090 Pesche (IS), Italy.
Georgios StrimpakosInstitute of Biochemistry and Cell Biology, National Research Council (CNR), 00015 Rome, Italy.ORCID 0000-0002-6021-9704
Barbara ColellaDepartment of Biosciences and Territory, University of Molise, 86090 Pesche (IS), Italy.
Paola TirassaInstitute of Biochemistry and Cell Biology, National Research Council (CNR), 00015 Rome, Italy.ORCID 0000-0002-8791-4424
Sabrina Di BartolomeoDepartment of Biosciences and Territory, University of Molise, 86090 Pesche (IS), Italy.ORCID 0000-0002-5748-1541
Marco SegattoDepartment of Biosciences and Territory, University of Molise, 86090 Pesche (IS), Italy.ORCID 0000-0003-0465-9470
University of Molise · ITNational Research Council · ITRoma Tre University · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite its undisputable role in the homeostatic regulation of the nervous system, the nerve growth factor (NGF) also governs the relevant cellular processes in other tissues and organs. In this study, we aimed at assessing the expression and the putative involvement of NGF signaling in skeletal muscle physiology. To reach this objective, we employed satellite cell-derived myoblasts as an in vitro culture model. In vivo experiments were performed on Tibialis anterior from wild-type mice and an mdx mouse model of Duchenne muscular dystrophy. Targets of interest were mainly assessed by means of morphological, Western blot and qRT-PCR analysis. The results show that proNGF is involved in myogenic differentiation. Importantly, the proNGF/p75NTR pathway orchestrates a slow-to-fast fiber type transition by counteracting the expression of slow myosin heavy chain and that of oxidative markers. Concurrently, proNGF/p75NTR activation facilitates the induction of fast myosin heavy chain and of fast/glycolytic markers. Furthermore, we also provided evidence that the oxidative metabolism is impaired in mdx mice, and that these alterations are paralleled by a prominent buildup of proNGF and p75NTR. These findings underline that the proNGF/p75NTR pathway may play a crucial role in fiber type determination and suggest its prospective modulation as an innovative therapeutic approach to counteract muscle disorders.

Indexed as

AnimalsCell DifferentiationHumansMiceMuscle, SkeletalNerve Growth FactorPhenotypeNerve Growth FactorNGF protein, humandifferentiationDuchenne muscular dystrophymetabolismmyotubesnerve growth factorneurotrophinsp75 NTRsatellite cellsskeletal muscle

Identifiers

PMID33023189
PMCPMC7599914
OpenAlexW3091188332

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.