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Cdk5 regulates IP3R1-mediated Ca(2+) dynamics and Ca(2+)-mediated cell proliferation
Loss of cyclin-dependent kinase 5 (Cdk5) in the mitochondria-associated endoplasmic reticulum (ER) membranes (MAMs) increases ER–mitochondria tethering and ER Ca(2+) transfer to the mitochondria, subsequently increasing mitochondrial Ca(2+) concentration ([Ca(2+)](mt)). This suggests a role for Cdk5...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9402492/ https://www.ncbi.nlm.nih.gov/pubmed/36001172 http://dx.doi.org/10.1007/s00018-022-04515-8 |
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author | NavaneethaKrishnan, Saranya Law, Vincent Lee, Jungkwon Rosales, Jesusa L. Lee, Ki-Young |
author_facet | NavaneethaKrishnan, Saranya Law, Vincent Lee, Jungkwon Rosales, Jesusa L. Lee, Ki-Young |
author_sort | NavaneethaKrishnan, Saranya |
collection | PubMed |
description | Loss of cyclin-dependent kinase 5 (Cdk5) in the mitochondria-associated endoplasmic reticulum (ER) membranes (MAMs) increases ER–mitochondria tethering and ER Ca(2+) transfer to the mitochondria, subsequently increasing mitochondrial Ca(2+) concentration ([Ca(2+)](mt)). This suggests a role for Cdk5 in regulating intracellular Ca(2+) dynamics, but how Cdk5 is involved in this process remains to be explored. Using ex vivo primary mouse embryonic fibroblasts (MEFs) isolated from Cdk5(−/−) mouse embryos, we show here that loss of Cdk5 causes an increase in cytosolic Ca(2+)concentration ([Ca(2+)](cyt)), which is not due to reduced internal Ca(2+) store capacity or increased Ca(2+) influx from the extracellular milieu. Instead, by stimulation with ATP that mediates release of Ca(2+) from internal stores, we determined that the rise in [Ca(2+)](cyt) in Cdk5(−/−) MEFs is due to increased inositol 1,4,5-trisphosphate receptor (IP3R)-mediated Ca(2+) release from internal stores. Cdk5 interacts with the IP3R1 Ca(2+) channel and phosphorylates it at Ser(421). Such phosphorylation controls IP3R1-mediated Ca(2+) release as loss of Cdk5, and thus, loss of IP3R1 Ser(421) phosphorylation triggers an increase in IP3R1-mediated Ca(2+) release in Cdk5(−/−) MEFs, resulting in elevated [Ca(2+)](cyt). Elevated [Ca(2+)](cyt) in these cells further induces the production of reactive oxygen species (ROS), which upregulates the levels of Nrf2 and its targets, Prx1 and Prx2. Cdk5(−/−) MEFs, which have elevated [Ca(2+)](cyt), proliferate at a faster rate compared to wt, and Cdk5(−/−) embryos have increased body weight and size compared to their wt littermates. Taken together, we show that altered IP3R1-mediated Ca(2+) dynamics due to Cdk5 loss correspond to accelerated cell proliferation that correlates with increased body weight and size in Cdk5(−/−) embryos. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00018-022-04515-8. |
format | Online Article Text |
id | pubmed-9402492 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-94024922022-08-26 Cdk5 regulates IP3R1-mediated Ca(2+) dynamics and Ca(2+)-mediated cell proliferation NavaneethaKrishnan, Saranya Law, Vincent Lee, Jungkwon Rosales, Jesusa L. Lee, Ki-Young Cell Mol Life Sci Original Article Loss of cyclin-dependent kinase 5 (Cdk5) in the mitochondria-associated endoplasmic reticulum (ER) membranes (MAMs) increases ER–mitochondria tethering and ER Ca(2+) transfer to the mitochondria, subsequently increasing mitochondrial Ca(2+) concentration ([Ca(2+)](mt)). This suggests a role for Cdk5 in regulating intracellular Ca(2+) dynamics, but how Cdk5 is involved in this process remains to be explored. Using ex vivo primary mouse embryonic fibroblasts (MEFs) isolated from Cdk5(−/−) mouse embryos, we show here that loss of Cdk5 causes an increase in cytosolic Ca(2+)concentration ([Ca(2+)](cyt)), which is not due to reduced internal Ca(2+) store capacity or increased Ca(2+) influx from the extracellular milieu. Instead, by stimulation with ATP that mediates release of Ca(2+) from internal stores, we determined that the rise in [Ca(2+)](cyt) in Cdk5(−/−) MEFs is due to increased inositol 1,4,5-trisphosphate receptor (IP3R)-mediated Ca(2+) release from internal stores. Cdk5 interacts with the IP3R1 Ca(2+) channel and phosphorylates it at Ser(421). Such phosphorylation controls IP3R1-mediated Ca(2+) release as loss of Cdk5, and thus, loss of IP3R1 Ser(421) phosphorylation triggers an increase in IP3R1-mediated Ca(2+) release in Cdk5(−/−) MEFs, resulting in elevated [Ca(2+)](cyt). Elevated [Ca(2+)](cyt) in these cells further induces the production of reactive oxygen species (ROS), which upregulates the levels of Nrf2 and its targets, Prx1 and Prx2. Cdk5(−/−) MEFs, which have elevated [Ca(2+)](cyt), proliferate at a faster rate compared to wt, and Cdk5(−/−) embryos have increased body weight and size compared to their wt littermates. Taken together, we show that altered IP3R1-mediated Ca(2+) dynamics due to Cdk5 loss correspond to accelerated cell proliferation that correlates with increased body weight and size in Cdk5(−/−) embryos. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00018-022-04515-8. Springer International Publishing 2022-08-24 2022 /pmc/articles/PMC9402492/ /pubmed/36001172 http://dx.doi.org/10.1007/s00018-022-04515-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 | Original Article NavaneethaKrishnan, Saranya Law, Vincent Lee, Jungkwon Rosales, Jesusa L. Lee, Ki-Young Cdk5 regulates IP3R1-mediated Ca(2+) dynamics and Ca(2+)-mediated cell proliferation |
title | Cdk5 regulates IP3R1-mediated Ca(2+) dynamics and Ca(2+)-mediated cell proliferation |
title_full | Cdk5 regulates IP3R1-mediated Ca(2+) dynamics and Ca(2+)-mediated cell proliferation |
title_fullStr | Cdk5 regulates IP3R1-mediated Ca(2+) dynamics and Ca(2+)-mediated cell proliferation |
title_full_unstemmed | Cdk5 regulates IP3R1-mediated Ca(2+) dynamics and Ca(2+)-mediated cell proliferation |
title_short | Cdk5 regulates IP3R1-mediated Ca(2+) dynamics and Ca(2+)-mediated cell proliferation |
title_sort | cdk5 regulates ip3r1-mediated ca(2+) dynamics and ca(2+)-mediated cell proliferation |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9402492/ https://www.ncbi.nlm.nih.gov/pubmed/36001172 http://dx.doi.org/10.1007/s00018-022-04515-8 |
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