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Amperometry methods for monitoring vesicular quantal size and regulation of exocytosis release

Chemical signaling strength during intercellular communication can be regulated by secretory cells through controlling the amount of signaling molecules that are released from a secretory vesicle during the exocytosis process. In addition, the chemical signal can also be influenced by the amount of...

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Detalles Bibliográficos
Autores principales: Fathali, Hoda, Cans, Ann-Sofie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5748430/
https://www.ncbi.nlm.nih.gov/pubmed/28951968
http://dx.doi.org/10.1007/s00424-017-2069-9
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author Fathali, Hoda
Cans, Ann-Sofie
author_facet Fathali, Hoda
Cans, Ann-Sofie
author_sort Fathali, Hoda
collection PubMed
description Chemical signaling strength during intercellular communication can be regulated by secretory cells through controlling the amount of signaling molecules that are released from a secretory vesicle during the exocytosis process. In addition, the chemical signal can also be influenced by the amount of neurotransmitters that is accumulated and stored inside the secretory vesicle compartment. Here, we present the development of analytical methodologies and cell model systems that have been applied in neuroscience research for gaining better insights into the biophysics and the molecular mechanisms, which are involved in the regulatory aspects of the exocytosis machinery affecting the output signal of chemical transmission at neuronal and neuroendocrine cells.
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spelling pubmed-57484302018-01-19 Amperometry methods for monitoring vesicular quantal size and regulation of exocytosis release Fathali, Hoda Cans, Ann-Sofie Pflugers Arch Invited Review Chemical signaling strength during intercellular communication can be regulated by secretory cells through controlling the amount of signaling molecules that are released from a secretory vesicle during the exocytosis process. In addition, the chemical signal can also be influenced by the amount of neurotransmitters that is accumulated and stored inside the secretory vesicle compartment. Here, we present the development of analytical methodologies and cell model systems that have been applied in neuroscience research for gaining better insights into the biophysics and the molecular mechanisms, which are involved in the regulatory aspects of the exocytosis machinery affecting the output signal of chemical transmission at neuronal and neuroendocrine cells. Springer Berlin Heidelberg 2017-09-27 2018 /pmc/articles/PMC5748430/ /pubmed/28951968 http://dx.doi.org/10.1007/s00424-017-2069-9 Text en © The Author(s) 2017 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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.
spellingShingle Invited Review
Fathali, Hoda
Cans, Ann-Sofie
Amperometry methods for monitoring vesicular quantal size and regulation of exocytosis release
title Amperometry methods for monitoring vesicular quantal size and regulation of exocytosis release
title_full Amperometry methods for monitoring vesicular quantal size and regulation of exocytosis release
title_fullStr Amperometry methods for monitoring vesicular quantal size and regulation of exocytosis release
title_full_unstemmed Amperometry methods for monitoring vesicular quantal size and regulation of exocytosis release
title_short Amperometry methods for monitoring vesicular quantal size and regulation of exocytosis release
title_sort amperometry methods for monitoring vesicular quantal size and regulation of exocytosis release
topic Invited Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5748430/
https://www.ncbi.nlm.nih.gov/pubmed/28951968
http://dx.doi.org/10.1007/s00424-017-2069-9
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