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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...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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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. |
format | Online Article Text |
id | pubmed-3854942 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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