Evidence map›Paper›PMID 32681815›Full record

ArticleJournal of cellular and molecular medicine2020

Gene expression profile of adhesion and extracellular matrix molecules during early stages of skeletal muscle regeneration.

Laura C Ceafalan, Maria Dobre, Elena Milanesi, Andrei M Niculae, Emilia Manole, Mihaela Gherghiceanu, Mihail E Hinescu

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

12 citing papers in PubMed, 15 citations in OpenAlex.

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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.

Laura C CeafalanCell Biology, Neurosciences and Experimental Myology Laboratory, 'Victor Babeș' National Institute of Pathology, Bucharest, Romania.ORCID 0000-0003-4952-9186
Maria DobreMolecular Pathology Laboratory, 'Victor Babeș' National Institute of Pathology, Bucharest, Romania.
Elena MilanesiMolecular Pathology Laboratory, 'Victor Babeș' National Institute of Pathology, Bucharest, Romania.
Andrei M NiculaeDepartment of Cellular and Molecular Biology and Histology, Faculty of Medicine, 'Carol Davila' University of Medicine and Pharmacy, Bucharest, Romania.
Emilia ManoleCell Biology, Neurosciences and Experimental Myology Laboratory, 'Victor Babeș' National Institute of Pathology, Bucharest, Romania.
Mihaela GherghiceanuDepartment of Cellular and Molecular Biology and Histology, Faculty of Medicine, 'Carol Davila' University of Medicine and Pharmacy, Bucharest, Romania.ORCID 0000-0001-6117-4328
Mihail E HinescuCell Biology, Neurosciences and Experimental Myology Laboratory, 'Victor Babeș' National Institute of Pathology, Bucharest, Romania.
Carol Davila University of Medicine and Pharmacy · ROInstitutul National Victor Babes · RO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Skeletal muscle regeneration implies the coordination of myogenesis with the recruitment of myeloid cells and extracellular matrix (ECM) remodelling. Currently, there are no specific biomarkers to diagnose the severity and prognosis of muscle lesions. In order to investigate the gene expression profile of extracellular matrix and adhesion molecules, as premises of homo- or heterocellular cooperation and milestones for skeletal muscle regeneration, we performed a gene expression analysis for genes involved in cellular cooperation, migration and ECM remodelling in a mouse model of acute crush injury. The results obtained at two early time-points post-injury were compared to a GSE5413 data set from two other trauma models. Third day post-injury, when inflammatory cells invaded, genes associated with cell-matrix interactions and migration were up-regulated. After day 5, as myoblast migration and differentiation started, genes for basement membrane constituents were found down-regulated, whereas genes for ECM molecules, macrophage, myoblast adhesion, and migration receptors were up-regulated. However, the profile and the induction time varied according to the experimental model, with only few genes being constantly up-regulated. Gene up-regulation was higher, delayed and more diverse following more severe trauma. Moreover, one of the most up-regulated genes was periostin, suggestive for severe muscle damage and unfavourable architecture restoration.

Indexed as

AnimalsBasement MembraneCell DifferentiationCell MovementDown-RegulationExtracellular MatrixExtracellular Matrix ProteinsMaleMiceMice, Inbred C57BLMuscle, SkeletalMyoblastsRegenerationTranscriptomeUp-RegulationExtracellular Matrix Proteinsadhesion moleculesextracellular matrix moleculesgene expression profileskeletal muscle regeneration

Identifiers

PMID32681815
PMCPMC7520258
OpenAlexW3043025286

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Registered trials

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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.