Cargando…

Vesicular control of fusion pore expansion

Exocytic post-fusion events play an important role determining the composition and quantity of cellular secretion. In particular, Ca(2+)-dependent regulation of fusion pore dilation/closure is a key regulator for fine-tuning vesicle content secretion. This requires a tight temporal and spatial integ...

Descripción completa

Detalles Bibliográficos
Autores principales: Neuland, Kathrin, Frick, Manfred
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4594593/
https://www.ncbi.nlm.nih.gov/pubmed/26479858
http://dx.doi.org/10.1080/19420889.2015.1018496
_version_ 1782393469674717184
author Neuland, Kathrin
Frick, Manfred
author_facet Neuland, Kathrin
Frick, Manfred
author_sort Neuland, Kathrin
collection PubMed
description Exocytic post-fusion events play an important role determining the composition and quantity of cellular secretion. In particular, Ca(2+)-dependent regulation of fusion pore dilation/closure is a key regulator for fine-tuning vesicle content secretion. This requires a tight temporal and spatial integration of vesicle fusion with the PM, Ca(2+) signals and translation of the Ca(2+) signal into fusion pore dilation via auxiliary factors. Yet, it is still mostly elusive how this is achieved in slow and non-excitable secretory cells, where initial Ca(2+) signals triggering fusions will abate before onset of the post-fusion phase. New results suggest, that the vesicles themselves provide the necessary itinerary to sense and link vesicle fusion to generation of local Ca(2+) signals and fusion pore expansion.
format Online
Article
Text
id pubmed-4594593
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Taylor & Francis
record_format MEDLINE/PubMed
spelling pubmed-45945932015-10-16 Vesicular control of fusion pore expansion Neuland, Kathrin Frick, Manfred Commun Integr Biol Article Addendum Exocytic post-fusion events play an important role determining the composition and quantity of cellular secretion. In particular, Ca(2+)-dependent regulation of fusion pore dilation/closure is a key regulator for fine-tuning vesicle content secretion. This requires a tight temporal and spatial integration of vesicle fusion with the PM, Ca(2+) signals and translation of the Ca(2+) signal into fusion pore dilation via auxiliary factors. Yet, it is still mostly elusive how this is achieved in slow and non-excitable secretory cells, where initial Ca(2+) signals triggering fusions will abate before onset of the post-fusion phase. New results suggest, that the vesicles themselves provide the necessary itinerary to sense and link vesicle fusion to generation of local Ca(2+) signals and fusion pore expansion. Taylor & Francis 2015-04-01 /pmc/articles/PMC4594593/ /pubmed/26479858 http://dx.doi.org/10.1080/19420889.2015.1018496 Text en © 2015 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
Neuland, Kathrin
Frick, Manfred
Vesicular control of fusion pore expansion
title Vesicular control of fusion pore expansion
title_full Vesicular control of fusion pore expansion
title_fullStr Vesicular control of fusion pore expansion
title_full_unstemmed Vesicular control of fusion pore expansion
title_short Vesicular control of fusion pore expansion
title_sort vesicular control of fusion pore expansion
topic Article Addendum
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4594593/
https://www.ncbi.nlm.nih.gov/pubmed/26479858
http://dx.doi.org/10.1080/19420889.2015.1018496
work_keys_str_mv AT neulandkathrin vesicularcontroloffusionporeexpansion
AT frickmanfred vesicularcontroloffusionporeexpansion