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Short Lives with Long-Lasting Effects: Filopodia Protrusions in Neuronal Branching Morphogenesis

The branching behaviors of both dendrites and axons are part of a neuronal maturation process initiated by the generation of small and transient membrane protrusions. These are highly dynamic, actin-enriched structures, collectively called filopodia, which can mature in neurons to form stable branch...

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Detalles Bibliográficos
Autores principales: Leondaritis, George, Eickholt, Britta Johanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4559444/
https://www.ncbi.nlm.nih.gov/pubmed/26334727
http://dx.doi.org/10.1371/journal.pbio.1002241
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author Leondaritis, George
Eickholt, Britta Johanna
author_facet Leondaritis, George
Eickholt, Britta Johanna
author_sort Leondaritis, George
collection PubMed
description The branching behaviors of both dendrites and axons are part of a neuronal maturation process initiated by the generation of small and transient membrane protrusions. These are highly dynamic, actin-enriched structures, collectively called filopodia, which can mature in neurons to form stable branches. Consequently, the generation of filopodia protrusions is crucial during the formation of neuronal circuits and involves the precise control of an interplay between the plasma membrane and actin dynamics. In this issue of PLOS Biology, Hou and colleagues identify a Ca(2+)/CaM-dependent molecular machinery in dendrites that ensures proper targeting of branch formation by activation of the actin nucleator Cobl.
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spelling pubmed-45594442015-09-10 Short Lives with Long-Lasting Effects: Filopodia Protrusions in Neuronal Branching Morphogenesis Leondaritis, George Eickholt, Britta Johanna PLoS Biol Primer The branching behaviors of both dendrites and axons are part of a neuronal maturation process initiated by the generation of small and transient membrane protrusions. These are highly dynamic, actin-enriched structures, collectively called filopodia, which can mature in neurons to form stable branches. Consequently, the generation of filopodia protrusions is crucial during the formation of neuronal circuits and involves the precise control of an interplay between the plasma membrane and actin dynamics. In this issue of PLOS Biology, Hou and colleagues identify a Ca(2+)/CaM-dependent molecular machinery in dendrites that ensures proper targeting of branch formation by activation of the actin nucleator Cobl. Public Library of Science 2015-09-03 /pmc/articles/PMC4559444/ /pubmed/26334727 http://dx.doi.org/10.1371/journal.pbio.1002241 Text en © 2015 Leondaritis, Eickholt http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Primer
Leondaritis, George
Eickholt, Britta Johanna
Short Lives with Long-Lasting Effects: Filopodia Protrusions in Neuronal Branching Morphogenesis
title Short Lives with Long-Lasting Effects: Filopodia Protrusions in Neuronal Branching Morphogenesis
title_full Short Lives with Long-Lasting Effects: Filopodia Protrusions in Neuronal Branching Morphogenesis
title_fullStr Short Lives with Long-Lasting Effects: Filopodia Protrusions in Neuronal Branching Morphogenesis
title_full_unstemmed Short Lives with Long-Lasting Effects: Filopodia Protrusions in Neuronal Branching Morphogenesis
title_short Short Lives with Long-Lasting Effects: Filopodia Protrusions in Neuronal Branching Morphogenesis
title_sort short lives with long-lasting effects: filopodia protrusions in neuronal branching morphogenesis
topic Primer
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4559444/
https://www.ncbi.nlm.nih.gov/pubmed/26334727
http://dx.doi.org/10.1371/journal.pbio.1002241
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