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Basolateral Mg(2+) Extrusion via CNNM4 Mediates Transcellular Mg(2+) Transport across Epithelia: A Mouse Model

Transcellular Mg(2+) transport across epithelia, involving both apical entry and basolateral extrusion, is essential for magnesium homeostasis, but molecules involved in basolateral extrusion have not yet been identified. Here, we show that CNNM4 is the basolaterally located Mg(2+) extrusion molecul...

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Autores principales: Yamazaki, Daisuke, Funato, Yosuke, Miura, Jiro, Sato, Sunao, Toyosawa, Satoru, Furutani, Kazuharu, Kurachi, Yoshihisa, Omori, Yoshihiro, Furukawa, Takahisa, Tsuda, Tetsuya, Kuwabata, Susumu, Mizukami, Shin, Kikuchi, Kazuya, Miki, Hiroaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3854942/
https://www.ncbi.nlm.nih.gov/pubmed/24339795
http://dx.doi.org/10.1371/journal.pgen.1003983
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author Yamazaki, Daisuke
Funato, Yosuke
Miura, Jiro
Sato, Sunao
Toyosawa, Satoru
Furutani, Kazuharu
Kurachi, Yoshihisa
Omori, Yoshihiro
Furukawa, Takahisa
Tsuda, Tetsuya
Kuwabata, Susumu
Mizukami, Shin
Kikuchi, Kazuya
Miki, Hiroaki
author_facet Yamazaki, Daisuke
Funato, Yosuke
Miura, Jiro
Sato, Sunao
Toyosawa, Satoru
Furutani, Kazuharu
Kurachi, Yoshihisa
Omori, Yoshihiro
Furukawa, Takahisa
Tsuda, Tetsuya
Kuwabata, Susumu
Mizukami, Shin
Kikuchi, Kazuya
Miki, Hiroaki
author_sort Yamazaki, Daisuke
collection PubMed
description Transcellular Mg(2+) transport across epithelia, involving both apical entry and basolateral extrusion, is essential for magnesium homeostasis, but molecules involved in basolateral extrusion have not yet been identified. Here, we show that CNNM4 is the basolaterally located Mg(2+) extrusion molecule. CNNM4 is strongly expressed in intestinal epithelia and localizes to their basolateral membrane. CNNM4-knockout mice showed hypomagnesemia due to the intestinal malabsorption of magnesium, suggesting its role in Mg(2+) extrusion to the inner parts of body. Imaging analyses revealed that CNNM4 can extrude Mg(2+) by exchanging intracellular Mg(2+) with extracellular Na(+). Furthermore, CNNM4 mutations cause Jalili syndrome, characterized by recessive amelogenesis imperfecta with cone-rod dystrophy. CNNM4-knockout mice showed defective amelogenesis, and CNNM4 again localizes to the basolateral membrane of ameloblasts, the enamel-forming epithelial cells. Missense point mutations associated with the disease abolish the Mg(2+) extrusion activity. These results demonstrate the crucial importance of Mg(2+) extrusion by CNNM4 in organismal and topical regulation of magnesium.
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spelling pubmed-38549422013-12-11 Basolateral Mg(2+) Extrusion via CNNM4 Mediates Transcellular Mg(2+) Transport across Epithelia: A Mouse Model Yamazaki, Daisuke Funato, Yosuke Miura, Jiro Sato, Sunao Toyosawa, Satoru Furutani, Kazuharu Kurachi, Yoshihisa Omori, Yoshihiro Furukawa, Takahisa Tsuda, Tetsuya Kuwabata, Susumu Mizukami, Shin Kikuchi, Kazuya Miki, Hiroaki PLoS Genet Research Article Transcellular Mg(2+) transport across epithelia, involving both apical entry and basolateral extrusion, is essential for magnesium homeostasis, but molecules involved in basolateral extrusion have not yet been identified. Here, we show that CNNM4 is the basolaterally located Mg(2+) extrusion molecule. CNNM4 is strongly expressed in intestinal epithelia and localizes to their basolateral membrane. CNNM4-knockout mice showed hypomagnesemia due to the intestinal malabsorption of magnesium, suggesting its role in Mg(2+) extrusion to the inner parts of body. Imaging analyses revealed that CNNM4 can extrude Mg(2+) by exchanging intracellular Mg(2+) with extracellular Na(+). Furthermore, CNNM4 mutations cause Jalili syndrome, characterized by recessive amelogenesis imperfecta with cone-rod dystrophy. CNNM4-knockout mice showed defective amelogenesis, and CNNM4 again localizes to the basolateral membrane of ameloblasts, the enamel-forming epithelial cells. Missense point mutations associated with the disease abolish the Mg(2+) extrusion activity. These results demonstrate the crucial importance of Mg(2+) extrusion by CNNM4 in organismal and topical regulation of magnesium. Public Library of Science 2013-12-05 /pmc/articles/PMC3854942/ /pubmed/24339795 http://dx.doi.org/10.1371/journal.pgen.1003983 Text en © 2013 Yamazaki et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Yamazaki, Daisuke
Funato, Yosuke
Miura, Jiro
Sato, Sunao
Toyosawa, Satoru
Furutani, Kazuharu
Kurachi, Yoshihisa
Omori, Yoshihiro
Furukawa, Takahisa
Tsuda, Tetsuya
Kuwabata, Susumu
Mizukami, Shin
Kikuchi, Kazuya
Miki, Hiroaki
Basolateral Mg(2+) Extrusion via CNNM4 Mediates Transcellular Mg(2+) Transport across Epithelia: A Mouse Model
title Basolateral Mg(2+) Extrusion via CNNM4 Mediates Transcellular Mg(2+) Transport across Epithelia: A Mouse Model
title_full Basolateral Mg(2+) Extrusion via CNNM4 Mediates Transcellular Mg(2+) Transport across Epithelia: A Mouse Model
title_fullStr Basolateral Mg(2+) Extrusion via CNNM4 Mediates Transcellular Mg(2+) Transport across Epithelia: A Mouse Model
title_full_unstemmed Basolateral Mg(2+) Extrusion via CNNM4 Mediates Transcellular Mg(2+) Transport across Epithelia: A Mouse Model
title_short Basolateral Mg(2+) Extrusion via CNNM4 Mediates Transcellular Mg(2+) Transport across Epithelia: A Mouse Model
title_sort basolateral mg(2+) extrusion via cnnm4 mediates transcellular mg(2+) transport across epithelia: a mouse model
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3854942/
https://www.ncbi.nlm.nih.gov/pubmed/24339795
http://dx.doi.org/10.1371/journal.pgen.1003983
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