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TRPM7-Mediated Ca(2+) Regulates Mussel Settlement through the CaMKKβ-AMPK-SGF1 Pathway
Many marine invertebrates have planktonic larval and benthic juvenile/adult stages. When the planktonic larvae are fully developed, they must find a favorable site to settle and metamorphose into benthic juveniles. This transition from a planktonic to a benthic mode of life is a complex behavioral p...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10049526/ https://www.ncbi.nlm.nih.gov/pubmed/36982474 http://dx.doi.org/10.3390/ijms24065399 |
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author | He, Jian Wang, Peng Wang, Zhixuan Feng, Danqing Zhang, Dun |
author_facet | He, Jian Wang, Peng Wang, Zhixuan Feng, Danqing Zhang, Dun |
author_sort | He, Jian |
collection | PubMed |
description | Many marine invertebrates have planktonic larval and benthic juvenile/adult stages. When the planktonic larvae are fully developed, they must find a favorable site to settle and metamorphose into benthic juveniles. This transition from a planktonic to a benthic mode of life is a complex behavioral process involving substrate searching and exploration. Although the mechanosensitive receptor in the tactile sensor has been implicated in sensing and responding to surfaces of the substrates, few have been unambiguously identified. Recently, we identified that the mechanosensitive transient receptor potential melastatin-subfamily member 7 (TRPM7) channel, highly expressed in the larval foot of the mussel Mytilospsis sallei, was involved in substrate exploration for settlement. Here, we show that the TRPM7-mediated Ca(2+) signal was involved in triggering the larval settlement of M. sallei through the calmodulin-dependent protein kinase kinase β/AMP-activated protein kinase/silk gland factor 1 (CaMKKβ-AMPK-SGF1) pathway. It was found that M. sallei larvae preferred the stiff surfaces for settlement, on which TRPM7, CaMKKβ, AMPK, and SGF1 were highly expressed. These findings will help us to better understand the molecular mechanisms of larval settlement in marine invertebrates, and will provide insights into the potential targets for developing environmentally friendly antifouling coatings for fouling organisms. |
format | Online Article Text |
id | pubmed-10049526 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-100495262023-03-29 TRPM7-Mediated Ca(2+) Regulates Mussel Settlement through the CaMKKβ-AMPK-SGF1 Pathway He, Jian Wang, Peng Wang, Zhixuan Feng, Danqing Zhang, Dun Int J Mol Sci Article Many marine invertebrates have planktonic larval and benthic juvenile/adult stages. When the planktonic larvae are fully developed, they must find a favorable site to settle and metamorphose into benthic juveniles. This transition from a planktonic to a benthic mode of life is a complex behavioral process involving substrate searching and exploration. Although the mechanosensitive receptor in the tactile sensor has been implicated in sensing and responding to surfaces of the substrates, few have been unambiguously identified. Recently, we identified that the mechanosensitive transient receptor potential melastatin-subfamily member 7 (TRPM7) channel, highly expressed in the larval foot of the mussel Mytilospsis sallei, was involved in substrate exploration for settlement. Here, we show that the TRPM7-mediated Ca(2+) signal was involved in triggering the larval settlement of M. sallei through the calmodulin-dependent protein kinase kinase β/AMP-activated protein kinase/silk gland factor 1 (CaMKKβ-AMPK-SGF1) pathway. It was found that M. sallei larvae preferred the stiff surfaces for settlement, on which TRPM7, CaMKKβ, AMPK, and SGF1 were highly expressed. These findings will help us to better understand the molecular mechanisms of larval settlement in marine invertebrates, and will provide insights into the potential targets for developing environmentally friendly antifouling coatings for fouling organisms. MDPI 2023-03-11 /pmc/articles/PMC10049526/ /pubmed/36982474 http://dx.doi.org/10.3390/ijms24065399 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article He, Jian Wang, Peng Wang, Zhixuan Feng, Danqing Zhang, Dun TRPM7-Mediated Ca(2+) Regulates Mussel Settlement through the CaMKKβ-AMPK-SGF1 Pathway |
title | TRPM7-Mediated Ca(2+) Regulates Mussel Settlement through the CaMKKβ-AMPK-SGF1 Pathway |
title_full | TRPM7-Mediated Ca(2+) Regulates Mussel Settlement through the CaMKKβ-AMPK-SGF1 Pathway |
title_fullStr | TRPM7-Mediated Ca(2+) Regulates Mussel Settlement through the CaMKKβ-AMPK-SGF1 Pathway |
title_full_unstemmed | TRPM7-Mediated Ca(2+) Regulates Mussel Settlement through the CaMKKβ-AMPK-SGF1 Pathway |
title_short | TRPM7-Mediated Ca(2+) Regulates Mussel Settlement through the CaMKKβ-AMPK-SGF1 Pathway |
title_sort | trpm7-mediated ca(2+) regulates mussel settlement through the camkkβ-ampk-sgf1 pathway |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10049526/ https://www.ncbi.nlm.nih.gov/pubmed/36982474 http://dx.doi.org/10.3390/ijms24065399 |
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