Evidence mapPaperPMID 41597236Full record

ArticleCells2026

RGMa Nuclear Localization in Skeletal Muscle Cells Reveals a Novel Role in Cell Viability and Proliferation.

Cristhian David Andrade Alfaro, Julia Meireles Nogueira, Christhiam Douglas Caetano Ribeiro, Kirsty Ximena Noboa Carrasco, Ana Luísa Cremonese Lubiana, Ana Maria Alvarenga Fagundes, Natália Paloma Vieira de Souza, Victor Rodrigues Santos, Carolina Cattoni Koh, Walderez Ornelas Dutra and 1 more

Abstract read
In one paragraph

Article in Cells, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Cristhian David Andrade AlfaroDepartamento de Morfologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Av. Pres. Antônio Carlos, 6627, Belo Horizonte 31270-901, MG, Brazil.ORCID 0009-0000-6783-899X
Julia Meireles NogueiraDepartamento de Morfologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Av. Pres. Antônio Carlos, 6627, Belo Horizonte 31270-901, MG, Brazil.
Christhiam Douglas Caetano RibeiroDepartamento de Morfologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Av. Pres. Antônio Carlos, 6627, Belo Horizonte 31270-901, MG, Brazil.ORCID 0000-0001-6362-7298
Kirsty Ximena Noboa CarrascoDepartamento de Morfologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Av. Pres. Antônio Carlos, 6627, Belo Horizonte 31270-901, MG, Brazil.ORCID 0009-0008-6175-0821
Ana Luísa Cremonese LubianaDepartamento de Morfologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Av. Pres. Antônio Carlos, 6627, Belo Horizonte 31270-901, MG, Brazil.
Ana Maria Alvarenga FagundesDepartamento de Morfologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Av. Pres. Antônio Carlos, 6627, Belo Horizonte 31270-901, MG, Brazil.
Natália Paloma Vieira de SouzaDepartamento de Morfologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Av. Pres. Antônio Carlos, 6627, Belo Horizonte 31270-901, MG, Brazil.
Victor Rodrigues SantosDepartamento de Morfologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Av. Pres. Antônio Carlos, 6627, Belo Horizonte 31270-901, MG, Brazil.ORCID 0000-0003-4979-3120
Carolina Cattoni KohDepartamento de Morfologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Av. Pres. Antônio Carlos, 6627, Belo Horizonte 31270-901, MG, Brazil.ORCID 0000-0001-8922-1667
Walderez Ornelas DutraDepartamento de Morfologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Av. Pres. Antônio Carlos, 6627, Belo Horizonte 31270-901, MG, Brazil.ORCID 0000-0002-7586-9996
Erika Cristina JorgeDepartamento de Morfologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Av. Pres. Antônio Carlos, 6627, Belo Horizonte 31270-901, MG, Brazil.ORCID 0000-0001-5390-5266

Funding

FAPEMIG APQ-01075-18
6 · The paper itself

Abstract

The Repulsive Guidance Molecule a (RGMa) is a multifunctional GPI-anchored protein localized in the sarcolemma and sarcoplasm of the adult skeletal muscle cell. Our research group showed that RGMa overexpression can promote myoblast fusion and induce hypertrophic muscle fibers during in vitro differentiation. Here, we report that RGMa is expressed in primary skeletal muscle cells cultured in vitro, showing a nuclear localization, revealed by immunostaining with an antibody targeting its C-terminal region (C-RGMa). While RGMa was detected in the nuclei, its canonical receptor, Neogenin, was predominantly found in the perinuclear region. Nuclear RGMa was absent in Neogenin-knockdown cells, suggesting that Neogenin mediates its nuclear transport. Functional assays suggested that RGMa promotes primary skeletal muscle cell viability and proliferation and supports their myogenic commitment. These findings reveal a previously unrecognized nuclear function of RGMa-Neogenin signaling and provide new insights into the regulation of skeletal muscle cell behavior in vitro.

Indexed as

Cell NucleusMuscle, SkeletalNerve Tissue ProteinsAnimalsCell DifferentiationCell ProliferationCells, CulturedCell SurvivalGPI-Linked ProteinsMembrane ProteinsMiceMuscle DevelopmentGPI-Linked ProteinsMembrane ProteinsneogeninNerve Tissue ProteinsRgma protein, mouseprimary skeletal muscle cellsprotein translocationrepulsive guidance moleculesubcellular compartment

Identifiers

PMID41597236
PMCPMC12839624

What Socratic holds

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LicenceCC BY
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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 Socratic graph.