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Morphoregulatory functions of the RNA-binding motif protein 3 in cell spreading, polarity and migration

RNA-binding proteins are emerging as key regulators of transitions in cell morphology. The RNA-binding motif protein 3 (RBM3) is a cold-inducible RNA-binding protein with broadly relevant roles in cellular protection, and putative functions in cancer and development. Several findings suggest that RB...

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Autores principales: Pilotte, J., Kiosses, W., Chan, S. W., Makarenkova, H. P., Dupont-Versteegden, E., Vanderklish, P. W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5943363/
https://www.ncbi.nlm.nih.gov/pubmed/29743635
http://dx.doi.org/10.1038/s41598-018-25668-2
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author Pilotte, J.
Kiosses, W.
Chan, S. W.
Makarenkova, H. P.
Dupont-Versteegden, E.
Vanderklish, P. W.
author_facet Pilotte, J.
Kiosses, W.
Chan, S. W.
Makarenkova, H. P.
Dupont-Versteegden, E.
Vanderklish, P. W.
author_sort Pilotte, J.
collection PubMed
description RNA-binding proteins are emerging as key regulators of transitions in cell morphology. The RNA-binding motif protein 3 (RBM3) is a cold-inducible RNA-binding protein with broadly relevant roles in cellular protection, and putative functions in cancer and development. Several findings suggest that RBM3 has morphoregulatory functions germane to its roles in these contexts. For example, RBM3 helps maintain the morphological integrity of cell protrusions during cell stress and disease. Moreover, it is highly expressed in migrating neurons of the developing brain and in cancer invadopodia, suggesting roles in migration. We here show that RBM3 regulates cell polarity, spreading and migration. RBM3 was present in spreading initiation centers, filopodia and blebs that formed during cell spreading in cell lines and primary myoblasts. Reducing RBM3 triggered exaggerated spreading, increased RhoA expression, and a loss of polarity that was rescued by Rho kinase inhibition and overexpression of CRMP2. High RBM3 expression enhanced the motility of cells migrating by a mesenchymal mode involving extension of long protrusions, whereas RBM3 knockdown slowed migration, greatly reducing the ability of cells to extend protrusions and impairing multiple processes that require directional migration. These data establish novel functions of RBM3 of potential significance to tissue repair, metastasis and development.
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spelling pubmed-59433632018-05-14 Morphoregulatory functions of the RNA-binding motif protein 3 in cell spreading, polarity and migration Pilotte, J. Kiosses, W. Chan, S. W. Makarenkova, H. P. Dupont-Versteegden, E. Vanderklish, P. W. Sci Rep Article RNA-binding proteins are emerging as key regulators of transitions in cell morphology. The RNA-binding motif protein 3 (RBM3) is a cold-inducible RNA-binding protein with broadly relevant roles in cellular protection, and putative functions in cancer and development. Several findings suggest that RBM3 has morphoregulatory functions germane to its roles in these contexts. For example, RBM3 helps maintain the morphological integrity of cell protrusions during cell stress and disease. Moreover, it is highly expressed in migrating neurons of the developing brain and in cancer invadopodia, suggesting roles in migration. We here show that RBM3 regulates cell polarity, spreading and migration. RBM3 was present in spreading initiation centers, filopodia and blebs that formed during cell spreading in cell lines and primary myoblasts. Reducing RBM3 triggered exaggerated spreading, increased RhoA expression, and a loss of polarity that was rescued by Rho kinase inhibition and overexpression of CRMP2. High RBM3 expression enhanced the motility of cells migrating by a mesenchymal mode involving extension of long protrusions, whereas RBM3 knockdown slowed migration, greatly reducing the ability of cells to extend protrusions and impairing multiple processes that require directional migration. These data establish novel functions of RBM3 of potential significance to tissue repair, metastasis and development. Nature Publishing Group UK 2018-05-09 /pmc/articles/PMC5943363/ /pubmed/29743635 http://dx.doi.org/10.1038/s41598-018-25668-2 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Pilotte, J.
Kiosses, W.
Chan, S. W.
Makarenkova, H. P.
Dupont-Versteegden, E.
Vanderklish, P. W.
Morphoregulatory functions of the RNA-binding motif protein 3 in cell spreading, polarity and migration
title Morphoregulatory functions of the RNA-binding motif protein 3 in cell spreading, polarity and migration
title_full Morphoregulatory functions of the RNA-binding motif protein 3 in cell spreading, polarity and migration
title_fullStr Morphoregulatory functions of the RNA-binding motif protein 3 in cell spreading, polarity and migration
title_full_unstemmed Morphoregulatory functions of the RNA-binding motif protein 3 in cell spreading, polarity and migration
title_short Morphoregulatory functions of the RNA-binding motif protein 3 in cell spreading, polarity and migration
title_sort morphoregulatory functions of the rna-binding motif protein 3 in cell spreading, polarity and migration
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5943363/
https://www.ncbi.nlm.nih.gov/pubmed/29743635
http://dx.doi.org/10.1038/s41598-018-25668-2
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