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Jaw1/LRMP increases Ca(2+) influx upon GPCR stimulation with heterogeneous effect on the activity of each ITPR subtype

Ca(2+) influx upon G protein-coupled receptor (GPCR) stimulation is observed as a cytosolic Ca(2+) concentration oscillation crucial to initiating downstream responses including cell proliferation, differentiation, and cell–cell communication. Although Jaw1 is known to interact with inositol 1,4,5-t...

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Autores principales: Okumura, Wataru, Kozono, Takuma, Sato, Hiroyuki, Matsui, Hitomi, Takagi, Tsubasa, Tonozuka, Takashi, Nishikawa, Atsushi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9177832/
https://www.ncbi.nlm.nih.gov/pubmed/35676525
http://dx.doi.org/10.1038/s41598-022-13620-4
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author Okumura, Wataru
Kozono, Takuma
Sato, Hiroyuki
Matsui, Hitomi
Takagi, Tsubasa
Tonozuka, Takashi
Nishikawa, Atsushi
author_facet Okumura, Wataru
Kozono, Takuma
Sato, Hiroyuki
Matsui, Hitomi
Takagi, Tsubasa
Tonozuka, Takashi
Nishikawa, Atsushi
author_sort Okumura, Wataru
collection PubMed
description Ca(2+) influx upon G protein-coupled receptor (GPCR) stimulation is observed as a cytosolic Ca(2+) concentration oscillation crucial to initiating downstream responses including cell proliferation, differentiation, and cell–cell communication. Although Jaw1 is known to interact with inositol 1,4,5-triphosphate receptor (ITPRs), Ca(2+) channels on the endoplasmic reticulum, the function of Jaw1 in the Ca(2+) dynamics with physiological stimulation remains unclear. In this study, using inducible Jaw1-expressing HEK293 cells, we showed that Jaw1 increases Ca(2+) influx by GPCR stimulation via changing the Ca(2+) influx oscillation pattern. Furthermore, we showed that Jaw1 increases the Ca(2+) release activity of all ITPR subtypes in a subtly different manner. It is well known that the Ca(2+) influx oscillation pattern varies from cell type to cell type, therefore these findings provide an insight into the relationship between the heterogeneous Ca(2+) dynamics and the specific ITPR and Jaw1 expression patterns.
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spelling pubmed-91778322022-06-10 Jaw1/LRMP increases Ca(2+) influx upon GPCR stimulation with heterogeneous effect on the activity of each ITPR subtype Okumura, Wataru Kozono, Takuma Sato, Hiroyuki Matsui, Hitomi Takagi, Tsubasa Tonozuka, Takashi Nishikawa, Atsushi Sci Rep Article Ca(2+) influx upon G protein-coupled receptor (GPCR) stimulation is observed as a cytosolic Ca(2+) concentration oscillation crucial to initiating downstream responses including cell proliferation, differentiation, and cell–cell communication. Although Jaw1 is known to interact with inositol 1,4,5-triphosphate receptor (ITPRs), Ca(2+) channels on the endoplasmic reticulum, the function of Jaw1 in the Ca(2+) dynamics with physiological stimulation remains unclear. In this study, using inducible Jaw1-expressing HEK293 cells, we showed that Jaw1 increases Ca(2+) influx by GPCR stimulation via changing the Ca(2+) influx oscillation pattern. Furthermore, we showed that Jaw1 increases the Ca(2+) release activity of all ITPR subtypes in a subtly different manner. It is well known that the Ca(2+) influx oscillation pattern varies from cell type to cell type, therefore these findings provide an insight into the relationship between the heterogeneous Ca(2+) dynamics and the specific ITPR and Jaw1 expression patterns. Nature Publishing Group UK 2022-06-08 /pmc/articles/PMC9177832/ /pubmed/35676525 http://dx.doi.org/10.1038/s41598-022-13620-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Okumura, Wataru
Kozono, Takuma
Sato, Hiroyuki
Matsui, Hitomi
Takagi, Tsubasa
Tonozuka, Takashi
Nishikawa, Atsushi
Jaw1/LRMP increases Ca(2+) influx upon GPCR stimulation with heterogeneous effect on the activity of each ITPR subtype
title Jaw1/LRMP increases Ca(2+) influx upon GPCR stimulation with heterogeneous effect on the activity of each ITPR subtype
title_full Jaw1/LRMP increases Ca(2+) influx upon GPCR stimulation with heterogeneous effect on the activity of each ITPR subtype
title_fullStr Jaw1/LRMP increases Ca(2+) influx upon GPCR stimulation with heterogeneous effect on the activity of each ITPR subtype
title_full_unstemmed Jaw1/LRMP increases Ca(2+) influx upon GPCR stimulation with heterogeneous effect on the activity of each ITPR subtype
title_short Jaw1/LRMP increases Ca(2+) influx upon GPCR stimulation with heterogeneous effect on the activity of each ITPR subtype
title_sort jaw1/lrmp increases ca(2+) influx upon gpcr stimulation with heterogeneous effect on the activity of each itpr subtype
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9177832/
https://www.ncbi.nlm.nih.gov/pubmed/35676525
http://dx.doi.org/10.1038/s41598-022-13620-4
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