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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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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. |
format | Online Article Text |
id | pubmed-9177832 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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