Basolateral Mg2+ Extrusion via CNNM4 Mediates Transcellular Mg2+ Transport across Epithelia: A Mouse Model

被引:125
作者
Yamazaki, Daisuke [1 ]
Funato, Yosuke [1 ]
Miura, Jiro [2 ]
Sato, Sunao [3 ]
Toyosawa, Satoru [3 ]
Furutani, Kazuharu [4 ]
Kurachi, Yoshihisa [4 ]
Omori, Yoshihiro [5 ,6 ]
Furukawa, Takahisa [5 ,7 ]
Tsuda, Tetsuya [8 ]
Kuwabata, Susumu [8 ]
Mizukami, Shin [9 ]
Kikuchi, Kazuya [9 ]
Miki, Hiroaki [1 ]
机构
[1] Osaka Univ, Microbial Dis Res Inst, Dept Cellular Regulat, Suita, Osaka 565, Japan
[2] Osaka Univ, Dent Hosp, Div Interdisciplinary Dent, Suita, Osaka, Japan
[3] Osaka Univ, Grad Sch Dent, Dept Oral Pathol, Suita, Osaka, Japan
[4] Osaka Univ, Grad Sch Med, Dept Pharmacol, Suita, Osaka, Japan
[5] Osaka Univ, Inst Prot Res, Lab Mol & Dev Biol, Suita, Osaka 565, Japan
[6] Japan Sci & Technol Corp, PRESTO, Kawaguchi, Saitama, Japan
[7] Japan Sci & Technol Corp, CREST, Kawaguchi, Saitama, Japan
[8] Osaka Univ, Grad Sch Engn, Dept Appl Chem, Suita, Osaka, Japan
[9] Osaka Univ, Grad Sch Engn, Div Adv Sci & Biotechnol, Suita, Osaka, Japan
来源
PLOS GENETICS | 2013年 / 9卷 / 12期
基金
日本学术振兴会;
关键词
CONE-ROD DYSTROPHY; MAGNESIUM TRANSPORT; RENAL-FAILURE; MUTATIONS; SLC41A1; PROTEIN; HOMEOSTASIS; TRPM6; HYPOMAGNESEMIA; PARACELLIN-1;
D O I
10.1371/journal.pgen.1003983
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Transcellular Mg2+ 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 Mg2+ 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 Mg2+ extrusion to the inner parts of body. Imaging analyses revealed that CNNM4 can extrude Mg2+ by exchanging intracellular Mg2+ 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 Mg2+ extrusion activity. These results demonstrate the crucial importance of Mg2+ extrusion by CNNM4 in organismal and topical regulation of magnesium.
引用
收藏
页数:14
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