Sodium-dependent vitamin C transporter-2 mediates vitamin C transport at the cortical nerve terminal

被引:6
作者
Pierce, Marquicia R. [1 ]
Raj, Amita [2 ]
Betke, Katherine M. [3 ]
Zeidan, L. Nora [4 ]
Matthies, Heinrich J. G. [1 ]
May, James M. [4 ]
机构
[1] Vanderbilt Univ, Dept Mol Physiol & Biophys, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Dept Neurosci, Nashville, TN 37235 USA
[3] Vanderbilt Univ, Med Ctr, Dept Pharmacol, Nashville, TN 37232 USA
[4] Vanderbilt Univ, Dept Med, Nashville, TN USA
关键词
synaptosome; antioxidant; ganglia; cortical neurons; membrane transport; ASCORBIC-ACID; RAT-BRAIN; NOREPINEPHRINE TRANSPORTER; ENDOTHELIAL-CELLS; OXIDATIVE STRESS; ASTROCYTES; SVCT2; EFFLUX; LOCALIZATION; MAINTENANCE;
D O I
10.1002/jnr.23669
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
It has been shown that vitamin C (VC) is transported at synaptic boutons, but how this occurs has not been elucidated. This study investigates the role of the sodium-dependent vitamin C transporter-2 (SVCT2) in transporting VC at the cortical nerve terminal. Immunostaining of cultured mouse superior cervical ganglion cells showed the SVCT2 to be expressed in presynaptic boutons, colocalizing with the vesicular monoamine transporter-2 and the norepinephrine transporter. Immunoblotting of enriched cortical synaptosomes demonstrated that the SVCT2 was enriched in presynaptic fractions, confirming a predominantly presynaptic location. In crude synaptosomes, known inhibitors of SVCT2 inhibited uptake of VC. Furthermore, the kinetic features of VC uptake were consistent with SVCT2-mediated function. VC was also found to efflux from synaptosomes by a mechanism not involving the SVCT2. Indeed, VC efflux was substantially offset by reuptake of VC on the SVCT2. The presence and function of the SVCT2 at the presynaptic nerve terminal suggest that it is the transporter responsible for recovery of VC released into the synaptic cleft. (c) 2015 Wiley Periodicals, Inc.
引用
收藏
页码:1881 / 1890
页数:10
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