Cloning and functional characterization of a high-affinity Na+/dicarboxylate cotransporter from mouse brain

被引:63
作者
Pajor, AM [1 ]
Gangula, R [1 ]
Yao, XZ [1 ]
机构
[1] Univ Texas, Med Branch, Dept Phys & Biophys, Galveston, TX 77555 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY | 2001年 / 280卷 / 05期
关键词
succinate; citrate; sodium; neurotransmitters; Xenopus oocytes;
D O I
10.1152/ajpcell.2001.280.5.C1215
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Neurons contain a high-affinity Na+/dicarboxylate cotransporter for absorption of neurotransmitter precursor substrates, such as alpha -ketoglutarate and malate, which are subsequently metabolized to replenish pools of neurotransmitters, including glutamate. We have isolated the cDNA coding for a high-affinity Na+/dicarboxylate cotransporter from mouse brain, called mNaDC-3. The mRNA coding for mNaDC-3 is found in brain and choroid plexus as well as in kidney and liver. The mNaDC-3 transporter has a broad substrate specificity for dicarboxylates, including succinate, alpha -ketoglutarate, fumarate, malate, and dimethylsuccinate. The transport of citrate is relatively insensitive to pH, but the transport of succinate is inhibited by acidic pH. The Michaelis-Menten constant for succinate in mNaDC-3 is 140 muM in transport assays and 16 mM at -250 mV in two-electrode voltage clamp assays. Transport is dependent on sodium, although lithium can partially substitute for sodium. In conclusion, mNaDC-3 likely codes for the high-affinity Na+/dicarboxylate cotransporter in brain, and it has some unusual electrical properties compared with the other members of the family.
引用
收藏
页码:C1215 / C1223
页数:9
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