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The initiation of post-synaptic protrusions

The post-synaptic spines of neuronal dendrites are highly elaborate membrane protrusions. Their anatomy, stability and density are intimately linked to cognitive performance. The morphological transitions of spines are powered by coordinated polymerization of actin filaments against the plasma membr...

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Detalles Bibliográficos
Autores principales: Hotulainen, Pirta, Saarikangas, Juha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4951170/
https://www.ncbi.nlm.nih.gov/pubmed/27489575
http://dx.doi.org/10.1080/19420889.2015.1125053
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author Hotulainen, Pirta
Saarikangas, Juha
author_facet Hotulainen, Pirta
Saarikangas, Juha
author_sort Hotulainen, Pirta
collection PubMed
description The post-synaptic spines of neuronal dendrites are highly elaborate membrane protrusions. Their anatomy, stability and density are intimately linked to cognitive performance. The morphological transitions of spines are powered by coordinated polymerization of actin filaments against the plasma membrane, but how the membrane-associated polymerization is spatially and temporally regulated has remained ill defined. Here, we discuss our recent findings showing that dendritic spines can be initiated by direct membrane bending by the I-BAR protein MIM/Mtss1. This lipid phosphatidylinositol (PI(4,5)P(2)) signaling-activated membrane bending coordinated spatial actin assembly and promoted spine formation. From recent advances, we formulate a general model to discuss how spatially concentrated protein-lipid microdomains formed by multivalent interactions between lipids and actin/membrane regulatory proteins might launch cell protrusions.
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spelling pubmed-49511702016-08-03 The initiation of post-synaptic protrusions Hotulainen, Pirta Saarikangas, Juha Commun Integr Biol Article Addendum The post-synaptic spines of neuronal dendrites are highly elaborate membrane protrusions. Their anatomy, stability and density are intimately linked to cognitive performance. The morphological transitions of spines are powered by coordinated polymerization of actin filaments against the plasma membrane, but how the membrane-associated polymerization is spatially and temporally regulated has remained ill defined. Here, we discuss our recent findings showing that dendritic spines can be initiated by direct membrane bending by the I-BAR protein MIM/Mtss1. This lipid phosphatidylinositol (PI(4,5)P(2)) signaling-activated membrane bending coordinated spatial actin assembly and promoted spine formation. From recent advances, we formulate a general model to discuss how spatially concentrated protein-lipid microdomains formed by multivalent interactions between lipids and actin/membrane regulatory proteins might launch cell protrusions. Taylor & Francis 2016-04-12 /pmc/articles/PMC4951170/ /pubmed/27489575 http://dx.doi.org/10.1080/19420889.2015.1125053 Text en © 2016 The Author(s). Published with license by Taylor & Francis Group, LLC http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License http://creativecommons.org/licenses/by-nc/3.0/, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted.
spellingShingle Article Addendum
Hotulainen, Pirta
Saarikangas, Juha
The initiation of post-synaptic protrusions
title The initiation of post-synaptic protrusions
title_full The initiation of post-synaptic protrusions
title_fullStr The initiation of post-synaptic protrusions
title_full_unstemmed The initiation of post-synaptic protrusions
title_short The initiation of post-synaptic protrusions
title_sort initiation of post-synaptic protrusions
topic Article Addendum
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4951170/
https://www.ncbi.nlm.nih.gov/pubmed/27489575
http://dx.doi.org/10.1080/19420889.2015.1125053
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