Glutamine uptake by neurons: Interaction of protons with system a transporters

被引:169
作者
Chaudhry, FA
Schmitz, D
Reimer, RJ
Larsson, P
Gray, AT
Nicoll, R
Kavanaugh, M
Edwards, RH
机构
[1] Univ Calif San Francisco, Sch Med, Dept Neurol, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Sch Med, Dept Pharmacol, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Sch Med, Dept Anesthesia, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Sch Med, Dept Physiol, Grad Program Neurosci, San Francisco, CA 94143 USA
[5] Univ Calif San Francisco, Sch Med, Dept Physiol, Grad Program Cell Biol & Biomed Sci, San Francisco, CA 94143 USA
[6] Oregon Hlth & Sci Univ, Vollum Inst, Portland, OR 97201 USA
关键词
glutamine-glutamate cycle; system A; system N; glutamine; synaptic transmission; H+ coupling;
D O I
10.1523/JNEUROSCI.22-01-00062.2002
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Astrocytes provide the glutamine required by neurons to synthesize glutamate and GABA. However, the mechanisms involved in glutamine transfer from glia to neurons have remained poorly understood. Recent work has implicated the System N transporter SN1 in the efflux of glutamine from astrocytes and the very closely related System A transporters SA1 and SA2 in glutamine uptake by neurons. To understand how these closely related proteins mediate flux in different directions, we have examined their ionic coupling. In contrast to the electroneutral exchange of H+ for Na+ and neutral amino acid catalyzed by SN1, we now show that SA1 and SA2 do not couple H+ movement to amino acid flux. As a result, SA1 and SA2 are electrogenic and do not mediate flux reversal as readily as SN1. Differences between System N and A transporters in coupling to H+ thus contribute to the delivery of glutamine from glia to neurons. Nonetheless, although they are not transported, H+ inhibit SA1 and SA2 by competing with Na+.
引用
收藏
页码:62 / 72
页数:11
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