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Intravital Two-photon Imaging of Ca(2+) signaling in Secretory Organs of Yellow Cameleon Transgenic Mice
Intracellular calcium ([Ca(2+)]i) signaling regulates physiological functions in most cells. In secretory organs, such as the pancreas, salivary gland, and lacrimal gland (LG), [Ca(2+)]i elevation in acinar cells triggers fluid secretion, which plays vital roles in the maintenance of functional heal...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6203801/ https://www.ncbi.nlm.nih.gov/pubmed/30367106 http://dx.doi.org/10.1038/s41598-018-34347-1 |
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author | Jin, Kai Imada, Toshihiro Nakamura, Shigeru Izuta, Yusuke Oonishi, Erina Shibuya, Michiko Sakaguchi, Hisayo Adachi, Takahiro Tsubota, Kazuo |
author_facet | Jin, Kai Imada, Toshihiro Nakamura, Shigeru Izuta, Yusuke Oonishi, Erina Shibuya, Michiko Sakaguchi, Hisayo Adachi, Takahiro Tsubota, Kazuo |
author_sort | Jin, Kai |
collection | PubMed |
description | Intracellular calcium ([Ca(2+)]i) signaling regulates physiological functions in most cells. In secretory organs, such as the pancreas, salivary gland, and lacrimal gland (LG), [Ca(2+)]i elevation in acinar cells triggers fluid secretion, which plays vital roles in the maintenance of functional health across the life-course. It is important to understand the secretory mechanism of secretory organs, but lack of analytic systems available for living animals limits the scope of research to gain deeper insights into the precise mechanism of secretion. We established an intravital imaging system for specific cell types of secretory organs to monitor the [Ca(2+)]i changes using mouse line expressing Yellow Cameleon 3.60, a genetically encoded Ca(2+) indicator. Elevation of [Ca(2+)]i in specific cell types of secretory organs could be monitored after cholinergic stimulation ex vivo and intravitally. We found that a marked attenuation of LG [Ca(2+)]i response to cholinergic stimulation was induced under pathological conditions by postganglionic denervation. Intravital Ca(2+) imaging in secretory organs will broaden our understanding of the cellular mechanisms in animal models of secretory diseases. |
format | Online Article Text |
id | pubmed-6203801 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-62038012018-10-31 Intravital Two-photon Imaging of Ca(2+) signaling in Secretory Organs of Yellow Cameleon Transgenic Mice Jin, Kai Imada, Toshihiro Nakamura, Shigeru Izuta, Yusuke Oonishi, Erina Shibuya, Michiko Sakaguchi, Hisayo Adachi, Takahiro Tsubota, Kazuo Sci Rep Article Intracellular calcium ([Ca(2+)]i) signaling regulates physiological functions in most cells. In secretory organs, such as the pancreas, salivary gland, and lacrimal gland (LG), [Ca(2+)]i elevation in acinar cells triggers fluid secretion, which plays vital roles in the maintenance of functional health across the life-course. It is important to understand the secretory mechanism of secretory organs, but lack of analytic systems available for living animals limits the scope of research to gain deeper insights into the precise mechanism of secretion. We established an intravital imaging system for specific cell types of secretory organs to monitor the [Ca(2+)]i changes using mouse line expressing Yellow Cameleon 3.60, a genetically encoded Ca(2+) indicator. Elevation of [Ca(2+)]i in specific cell types of secretory organs could be monitored after cholinergic stimulation ex vivo and intravitally. We found that a marked attenuation of LG [Ca(2+)]i response to cholinergic stimulation was induced under pathological conditions by postganglionic denervation. Intravital Ca(2+) imaging in secretory organs will broaden our understanding of the cellular mechanisms in animal models of secretory diseases. Nature Publishing Group UK 2018-10-26 /pmc/articles/PMC6203801/ /pubmed/30367106 http://dx.doi.org/10.1038/s41598-018-34347-1 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 Jin, Kai Imada, Toshihiro Nakamura, Shigeru Izuta, Yusuke Oonishi, Erina Shibuya, Michiko Sakaguchi, Hisayo Adachi, Takahiro Tsubota, Kazuo Intravital Two-photon Imaging of Ca(2+) signaling in Secretory Organs of Yellow Cameleon Transgenic Mice |
title | Intravital Two-photon Imaging of Ca(2+) signaling in Secretory Organs of Yellow Cameleon Transgenic Mice |
title_full | Intravital Two-photon Imaging of Ca(2+) signaling in Secretory Organs of Yellow Cameleon Transgenic Mice |
title_fullStr | Intravital Two-photon Imaging of Ca(2+) signaling in Secretory Organs of Yellow Cameleon Transgenic Mice |
title_full_unstemmed | Intravital Two-photon Imaging of Ca(2+) signaling in Secretory Organs of Yellow Cameleon Transgenic Mice |
title_short | Intravital Two-photon Imaging of Ca(2+) signaling in Secretory Organs of Yellow Cameleon Transgenic Mice |
title_sort | intravital two-photon imaging of ca(2+) signaling in secretory organs of yellow cameleon transgenic mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6203801/ https://www.ncbi.nlm.nih.gov/pubmed/30367106 http://dx.doi.org/10.1038/s41598-018-34347-1 |
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