Identification of the differentiation-associated Na+/PI transporter as a novel vesicular glutamate transporter expressed in a distinct set of glutamatergic synapses

被引:376
作者
Varoqui, H
Schäfer, MKH
Zhu, HM
Weihe, E
Erickson, JD
机构
[1] Louisiana State Univ, Hlth Sci Ctr, Ctr Neurosci, New Orleans, LA 70112 USA
[2] Louisiana State Univ, Hlth Sci Ctr, Dept Ophthalmol, New Orleans, LA 70112 USA
[3] Louisiana State Univ, Hlth Sci Ctr, Dept Pharmacol, New Orleans, LA 70112 USA
[4] Univ Marburg, Inst Anat & Cell Biol, Dept Mol Neurosci, D-35033 Marburg, Germany
关键词
DNPI; BNPI; VGLUT1; VGLUT2; synaptic vesicle; excitatory synapse; vesicular glutamate transporter; glutamate release; chloride ion; synaptic plasticity; release probability;
D O I
10.1523/JNEUROSCI.22-01-00142.2002
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Glutamate transport into synaptic vesicles is a prerequisite for its regulated neurosecretion. Here we functionally identify a second isoform of the vesicular glutamate transporter (VGLUT2) that was previously identified as a plasma membrane Na+-dependent inorganic phosphate transporter (differentiation-associated Na+/P-I transporter). Studies using intracellular vesicles from transiently transfected PC12 cells indicate that uptake by VGLUT2 is highly selective for glutamate, is H+ dependent, and requires Cl- ion. Both the vesicular membrane potential (Delta psi) and the proton gradient (Delta pH) are important driving forces for vesicular glutamate accumulation under physiological Cl- concentrations. Using an antibody specific for VGLUT2, we also find that this protein is enriched on synaptic vesicles and selective for a distinct class of glutamatergic nerve terminals. The pathway-specific, complementary expression of two different vesicular glutamate transporters suggests functional diversity in the regulation of vesicular release at excitatory synapses. Together, the two isoforms may account for the uptake of glutamate by synaptic vesicles from all central glutamatergic neurons.
引用
收藏
页码:142 / 155
页数:14
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