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RGMa can induce skeletal muscle cell hyperplasia via association with neogenin signalling pathway
by
do Carmo Costa, Alinne
, Copola, Aline Gonçalves Lio
, Carvalho e Souza, Clara
, Jorge, Erika Cristina
, Nogueira, Júlia Meireles
, Silva, Gerluza Aparecida Borges
in
adults
/ Animal Genetics and Genomics
/ Biomedical and Life Sciences
/ Cell adhesion & migration
/ Cell Biology
/ Cell Culture
/ Cell differentiation
/ Cell fusion
/ CELL GROWTH/DIFFERENTIATION/APOPTOSIS
/ Cytoskeleton
/ Developmental Biology
/ Differentiation (biology)
/ Down-regulation
/ Hyperplasia
/ Hypertrophy
/ Life Sciences
/ Markers
/ muscle development
/ Muscles
/ Musculoskeletal system
/ Myoblasts
/ Myogenesis
/ Nervous system
/ Proteins
/ Receptors
/ recombinant proteins
/ Signal transduction
/ Signaling
/ Skeletal muscle
/ Somites
/ Stem Cells
2021
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RGMa can induce skeletal muscle cell hyperplasia via association with neogenin signalling pathway
by
do Carmo Costa, Alinne
, Copola, Aline Gonçalves Lio
, Carvalho e Souza, Clara
, Jorge, Erika Cristina
, Nogueira, Júlia Meireles
, Silva, Gerluza Aparecida Borges
in
adults
/ Animal Genetics and Genomics
/ Biomedical and Life Sciences
/ Cell adhesion & migration
/ Cell Biology
/ Cell Culture
/ Cell differentiation
/ Cell fusion
/ CELL GROWTH/DIFFERENTIATION/APOPTOSIS
/ Cytoskeleton
/ Developmental Biology
/ Differentiation (biology)
/ Down-regulation
/ Hyperplasia
/ Hypertrophy
/ Life Sciences
/ Markers
/ muscle development
/ Muscles
/ Musculoskeletal system
/ Myoblasts
/ Myogenesis
/ Nervous system
/ Proteins
/ Receptors
/ recombinant proteins
/ Signal transduction
/ Signaling
/ Skeletal muscle
/ Somites
/ Stem Cells
2021
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RGMa can induce skeletal muscle cell hyperplasia via association with neogenin signalling pathway
by
do Carmo Costa, Alinne
, Copola, Aline Gonçalves Lio
, Carvalho e Souza, Clara
, Jorge, Erika Cristina
, Nogueira, Júlia Meireles
, Silva, Gerluza Aparecida Borges
in
adults
/ Animal Genetics and Genomics
/ Biomedical and Life Sciences
/ Cell adhesion & migration
/ Cell Biology
/ Cell Culture
/ Cell differentiation
/ Cell fusion
/ CELL GROWTH/DIFFERENTIATION/APOPTOSIS
/ Cytoskeleton
/ Developmental Biology
/ Differentiation (biology)
/ Down-regulation
/ Hyperplasia
/ Hypertrophy
/ Life Sciences
/ Markers
/ muscle development
/ Muscles
/ Musculoskeletal system
/ Myoblasts
/ Myogenesis
/ Nervous system
/ Proteins
/ Receptors
/ recombinant proteins
/ Signal transduction
/ Signaling
/ Skeletal muscle
/ Somites
/ Stem Cells
2021
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RGMa can induce skeletal muscle cell hyperplasia via association with neogenin signalling pathway
Journal Article
RGMa can induce skeletal muscle cell hyperplasia via association with neogenin signalling pathway
2021
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Overview
Although originally discovered inducing important biological functions in the nervous system, repulsive guidance molecule a (RGMa) has now been identified as a player in many other processes and diseases, including in myogenesis. RGMa is known to be expressed in skeletal muscle cells, from somites to the adult. Functional in vitro studies have revealed that RGMa overexpression could promote skeletal muscle cell hypertrophy and hyperplasia, as higher efficiency in cell fusion was observed. Here, we extend the potential role of RGMa during C2C12 cell differentiation in vitro. Our results showed that RGMa administrated as a recombinant protein during late stages of C2C12 myogenic differentiation could induce myoblast cell fusion and the downregulation of different myogenic markers, while its administration at early stages induced the expression of myogenic markers with no detectable morphological effects. We also found that RGMa effects on skeletal muscle hyperplasia are performed via neogenin receptor, possibly as part of a complex with other proteins. Additionally, we observed that RGMa-neogenin is not playing a role as an inhibitor of the BMP signalling in skeletal muscle cells. This work contributes to placing RGMa as a component of the mechanisms that determine skeletal cell fusion via neogenin receptor.
Publisher
Springer Science & Business Media LLC,Springer US,Society for In Vitro Biology
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