QUICK SEARCH:   [advanced] Author: Keyword(s): Year:  Vol:  Page:

This Article Abstract Full Text (PDF) Purchase Article View Shopping Cart Alert me when this article is cited Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via HighWire Citing Articles via Google Scholar Google Scholar Articles by Colvin, R. A. Articles by Carter, P. A. Search for Related Content PubMed PubMed Citation Articles by Colvin, R. A. Articles by Carter, P. A.

---

Supplement

Zinc Transport in the Brain: Routes of Zinc Influx and Efflux in Neurons^{1 ,2}

Department of Biological Sciences, Program in Neuroscience, Ohio University Athens, OH 45701

³To whom correspondence should be addressed.

	ABSTRACT

TOP ABSTRACT INTRODUCTION Histochemically detectable zinc Future studies REFERENCES

 
Studies of the routes of entry and exit for zinc in different tissues and cell types have shown that zinc can use several pathways of exit or entry. In neurons, known pathways include (1) presynaptic release along with glutamate when synaptic vesicles empty their contents into the synaptic cleft, (2) voltage-gated L-type Ca²⁺ channels and glutamate-gated channels that provide an entry route when cells are depolarized and that mediate extracellular zinc toxicity and (3) a plasma membrane transporter potentially present in all neurons important for cellular zinc homeostasis. The least understood of these pathways, in terms of mechanism, is the transporter pathway. The kinetics of zinc uptake in cultured neurons under resting conditions are consistent with and suggest the existence of a saturable transporter in the plasma membrane. The proteins responsible for plasma membrane zinc transport have not yet been definitely identified. Likely candidates include two proteins identified by molecular cloning termed zinc transporter 1 and divalent cation transporter DCT1. Both proteins have been shown to be expressed in the brain, but only DCT1 is clearly demonstrated to be a transport protein, whereas zinc transporter 1 may only modulate zinc transport in association with as-yet-unidentified proteins. Understanding the mechanism and neuromodulation of plasma membrane zinc transport will be an important first step toward a complete understanding of neuronal zinc homeostasis.

KEY WORDS: • zinc • ion transport • heavy metal ions • trace elements • metal transporters • rat

	INTRODUCTION

TOP ABSTRACT INTRODUCTION Histochemically detectable zinc Future studies REFERENCES

 
Large amounts of zinc are present in the brain, yet very little is actually known about the molecular events underlying cellular zinc homeostasis and the functional role played by zinc in synaptic signaling (for several excellent recent reviews, see Choi and Koh 1998 , Cuajungco and Lees 1997 , Huang 1997 , McMahon and Cousins 1998 , Reyes 1996 ). Most of that zinc is tightly bound to metalloenzymes where zinc is involved as a cofactor in important functions such as gene expression or enzymatic reactions. However, a considerable amount, estimated to be as much as 10% of total brain zinc, is in a highly localized pool that can be detected by histochemical stains for metal ions. The chelatable pool is localized to synaptic vesicles, may be released on excitation and may play a role in modulation of synaptic signaling. Most cells, and neurons are no exception, must maintain cellular zinc content within a very narrow window, because low zinc levels inhibit cell growth and division and can lead to cell death and because high zinc levels are toxic. This presents the neuron with a very difficult problem to solve. Each neuron must be able to juggle the requirement for zinc and its constant turnover (which is particularly true of neurons, which presumably release zinc stored in vesicles on excitation) with the need to maintain zinc levels within narrow limits. It will not be surprising, therefore, if neurons in particular have a large complement of zinc homeostatic mechanisms at their disposal. It is known that neurons contain a ubiquitous zinc binding protein called metallothionein III (Erickson et al. 1997 ) that is thought to be very important in buffering cytoplasmic levels of zinc. When expressed in cultured cells, metallothionein can confer resistance to extracellular zinc toxicity (Palmiter 1998 ). Zinc is also known to be sequestered in synaptic vesicles, and this process may be stimulated when neurons are grown in zinc-containing media (Palmiter et al. 1996a ). Just as important as these homeostatic processes is the control of zinc influx and efflux across the plasma membrane. Zinc-specific or nonspecific divalent cation transporters, or both, and ion channels are thought to provide entry and exit routes for zinc. The focus of this report is to describe what is known about the mechanisms of zinc entry and exit from neurons.

	Histochemically detectable zinc

TOP ABSTRACT INTRODUCTION Histochemically detectable zinc Future studies REFERENCES

 
Released zinc may play a neuromodulatory role.

Approximately 10% of the total brain zinc is in a histochemically reactive chelatable pool (Fredrickson et al. 1983 ). Particularly in hippocampal mossy fibers, this zinc is localized to the lumen of glutamate containing synaptic vesicles. When these fibers are stimulated by K⁺ depolarization, kainic acid treatment or electrically, it is possible to detect zinc release and the depletion of the histochemically reactive zinc pool (Aniksztein et al. 1987 , Assaf and Chung 1984 , Charton et al. 1985 , Howell et al. 1984 ). Although not proven, it is presumed that such zinc release is the result of synaptic vesicle fusion with the presynaptic membrane. Large amounts of zinc are thought to be released along with glutamate, so it has been hypothesized that zinc could play an important neuromodulatory role at glutamatergic synapses. In support of this notion, micromolar concentrations of zinc have been shown to inhibit N-methyl-D-aspartate (NMDA)⁴ receptors (Chen et al. 1997 , Paoletti et al. 1997 , Traynelis et al. 1998 ). Two modes of inhibition exist that are either voltage dependent or voltage independent. The NR1 subunit appears to play a critical role in determining the sensitivity to zinc. In addition, zinc blocks -aminobutyric acid_A receptor currents (Berger et al. 1998 , Fisher and MacDonald 1998 ), the glutamate transporter EAAT1 (Vandenberg et al. 1998 ) and the dopamine transporter (Norregaard et al. 1998 ). Released zinc is then taken back up into neurons to replenish depleted synaptic vesicle stores (Howell et al. 1984 , Perez-Clausell and Danscher 1986 ). The process of neuronal uptake of zinc is mediated by a saturable transporter in the plasma membrane (see later) with a zinc affinity in the range of 20 µmol/l (Colvin 1998a , Colvin et al. 2000 , Howell et al. 1984 , Wensink et al. 1988 ).

Depolarized neurons exhibit rapid zinc uptake that can be associated with excitotoxicity.

Cortical neurons in primary culture have provided a useful model system in which to study depolarization-induced zinc entry. This type of movement of zinc across the plasma membrane may have immense pathophysiological significance, because this is thought to be the means by which zinc contributes to excitotoxicity (Koh et al. 1996 ). Studies have shown that when cells incubated in high concentrations of zinc are excited with glutamate, zinc rapidly enters the cell, and intracellular concentrations of zinc increase significantly and can reach levels that are toxic (Koh and Choi 1994 , Sensi et al. 1997 ). Depolarization-induced zinc influx is probably mediated primarily by L-type dihydropyridine-sensitive Ca²⁺ channels, because K⁺-stimulated neuronal ⁶⁵Zn²⁺ uptake and toxicity are blocked by nimodipine, verapamil or 10 µmol/l Gd³⁺ and only partially blocked by -conotoxin GVIA (Sensi et al. 1997 ). Increasing extracellular Ca²⁺ to 10–20 mmol/l reduced zinc-induced neuronal death consistent with a competition between zinc and calcium for entry routes (Koh and Choi 1994 ). Zinc-induced neurotoxicity showed sensitivity to NMDA channel antagonists (Koh and Choi 1994 ), suggesting that zinc entry can also occur via glutamate-activated channels. The application of either NMDA or kainate to cortical cells in the presence of 300 µmol/l zinc resulted in a rapid elevation in intracellular zinc. Glutamate agonist–induced zinc uptake was blocked by the addition of the corresponding antagonists [i.e., D2-amino-5-phosphonopentanoate and 1,2,3,4-tetrahydro-6-nitro-2,3-dioxo-benzo[f]quinoxaline-7-sulfonamide. It should be noted, however, that entry through Ca²⁺ channels also contributes to the rise in intracellular zinc after kainate exposure (Sensi et al. 1997 ). Using the fluorescent dye mag-Fura-5, cell body zinc was estimated to reach a maximum of 50 nmol/l under these conditions. A small apparent Na⁺/Zn²⁺ exchange current was observed in cortical neurons when extracellular Na⁺ was held at zero (Sensi et al. 1997 ). This exchange current was completely inhibited by 300 µmol/l benzamil. These data suggest that zinc may substitute for Ca²⁺ in the Na⁺/Ca²⁺ exchange transport mechanism. However, micromolar concentrations of zinc inhibit ⁴⁵Ca²⁺ transport by the Na⁺/Ca²⁺ exchanger in a manner that is not consistent with competitive kinetics (Colvin 1998b ).

Resting neurons slowly accumulate zinc.

Zinc uptake in resting cultured neurons probably represents transporter-mediated zinc uptake. Resting zinc uptake was measured in cultured cortical neurons by incubating neurons in a physiological buffer (modified Lock’s buffer) containing various concentrations of ⁶⁵Zn²⁺. These studies show that cultured neurons slowly accumulate ⁶⁵Zn²⁺ under these conditions and that a steady state ⁶⁵Zn²⁺ content is obtained after several hours of incubation. Shown in Figure 1 is the concentration dependence of ⁶⁵Zn²⁺ uptake measured in cultured neurons that had been exposed to ⁶⁵Zn²⁺-containing buffers for 15 min at 37°C. Zinc uptake clearly shows saturation kinetics, and the apparent K_m value is 10–20 µmol/l. Lanthanum (maximal effect seen at 5 mmol/l) inhibits a portion of ⁶⁵Zn²⁺ uptake. The data presented in Figure 1 represent La³⁺-sensitive ⁶⁵Zn²⁺ uptake. The nature of the La³⁺-insensitive ⁶⁵Zn²⁺ uptake is still unclear. Figure 2 shows the time course of ⁶⁵Zn²⁺ uptake in the presence of 5 mmol/l La³⁺. Over the range of zinc concentrations used (10–65 µmol/l) in these studies, a substantial amount of the total uptake of ⁶⁵Zn²⁺ is La³⁺ insensitive. However, a comparison of Figures 1 & 2 shows that important differences exist between La³⁺-sensitive and - insensitive ⁶⁵Zn²⁺ uptake. Figure 2 shows that La³⁺-insensitive uptake was very rapid and nearly complete within the first time point assayed (15 min). This finding contrasts with that seen for La³⁺-sensitive ⁶⁵Zn²⁺ uptake, where uptake continues for several hours. Another important difference is that over the concentration range studied (10–65 µmol/l), La³⁺-insensitive ⁶⁵Zn²⁺ uptake appears to be nearly saturated. The above results provide evidence for a binding site for ⁶⁵Zn²⁺ in cultured neurons with submicromolar affinity. This binding site may be on the cell surface, as the rapid time course argues against cellular accumulation. In the uptake assay, the cells are washed three times with 1 mmol/l EGTA before cells are lysed and ⁶⁵Zn²⁺ content is determined, so if La³⁺-insensitive ⁶⁵Zn²⁺ uptake represents surface binding, it would have to be occluded in some way. The addition of the heavy metal chelator o-phenanthroline to the uptake reaction blocked nearly all of the La³⁺-insensitive ⁶⁵Zn²⁺ uptake (Fig. 3 ).

View larger version (12K): [in this window] [in a new window]   Figure 1. 65Zn2+ uptake was measured in cortical neurons in primary culture 4 d after plating. Uptake assays were performed in 1 ml of modified Locke’s solution containing 154 mmol/l NaCl, 5.6 mmol/l KCl, 5.0 mmol/l HEPES, pH 7.4 and 10 mmol/l glucose containing varying concentrations of ZnCl2 and 65Zn2+ (4 µCi/ml). After 15 min at 37°C, the medium was removed, and 2 ml of ice-cold stop solution was added that contained modified Locke’s solution (without zinc) as given earlier with 5 mmol/l La3+. The cells were washed three times with 2 ml of wash buffer containing modified Locke’s solution (without zinc) and 1 mmol/l EGTA. Cells were lysed in 0.5 N NaOH, and all lysates were assayed for 65Zn2+ by gamma counting. Proteins were determined according to the Lowry method. Parallel experiments were performed with the addition of 5 mmol/l La3+, and these values were subtracted from total 65Zn2+ uptake to obtain the values plotted. Each point represents the mean and ± SE of duplicate determinations.

View larger version (14K): [in this window] [in a new window]   Figure 2. Cortical neurons in primary culture were incubated at 37°C for 15, 30, 60 and 120 min in 1 ml of modified Locke’s solution described in the legend to Figure 1 except 5 mmol/l La3+ was included. The concentrations of ZnCl2 used were 10, 30 and 65µmol/l. Each point represents the mean ± SE of triplicate determinations.

View larger version (14K): [in this window] [in a new window]   Figure 3. 65Zn2+ uptake was assayed as described in the legend to Figure 1 without the addition of lanthanum. The cells were incubated in 1 ml of modified Locke’s solution (Fig. 1) adjusted to the pH indicated containing 20 µmol/l ZnCl2 for 15 min. The concentration of o-phenanthroline was 1 mmol/l. Each point represents the mean ± SE of duplicate determinations.

To test the effect of various channel blockers on ⁶⁵Zn²⁺ uptake, purified plasma membrane vesicles were used and the results of these experiments are shown in Figure 4 . Appropriate blockers were chosen to block all the known routes of depolarization-induced zinc uptake (see earlier). None of these blockers had any effect on resting ⁶⁵Zn²⁺ accumulation (either La³⁺ sensitive or insensitive). These findings support the notion that a distinct plasma membrane transporter is mediating ⁶⁵Zn²⁺ uptake under these conditions.

View larger version (24K): [in this window] [in a new window]   Figure 4. 65Zn2+ uptake was measured, and plasma membrane vesicles were purified from rat brain. Vesicles were incubated in 137 mmol/l KCl and 10 mmol/l HEPES, pH 7.4, for 5 min at 37°C. The concentration of ZnCl2/65Zn2+ was 20 µmol/l. Parallel experiments were performed that included 1 mmol/l La3+ from the start of the reaction. To stop the reaction, La3+-containing tubes were placed on ice. To stop the reaction in tubes without La3+, ice-cold La3+ was added to a final concentration of 1 mmol/l. Vesicles were immediately filtered on GFC filters and washed four times with an ice-cold buffer containing 137 mmol/l choline Cl, 1 mmol/l EGTA and 10 mmol/l HEPES, pH 7.4. Each blocker was tested for its effects at the following concentrations: MK-801, 100 µmol/l; GYKI 52466, 100 µmol/l; nifedipine, 10 µmol/l; FTX-3.3, 1 µmol/l; and -conotoxin GVIA, 1 µmol/l. Each point represents the mean ± SE of duplicate determinations.

The first demonstration of a cloned gene that codes for a protein that is likely to transport zinc across the plasma membrane was achieved only recently by Gunshin et al. (1997 ). They used the heterologous expression system of Xenopus oocytes to isolate a nonspecific divalent cation transporter they termed DCT1. In oocytes injected with DCT1 mRNA, 50 µmol/l Fe²⁺ induced a large inward current enhanced by lowering extracellular pH from 7.4 to 5.5. Large inward currents were obtained when Zn²⁺, Mn²⁺, Cu²⁺, Co²⁺ or Cd²⁺ was used, and lesser currents were obtained when Ni²⁺ and Pb²⁺ were used. Pre–steady state currents suggested that H⁺ may bind to the transporter. Steady state currents were half-maximal at Fe²⁺ = 2 µmol/l. ⁵⁵Fe²⁺ uptake in NaCl-containing medium was the same as that seen in NaNO₃, NaSCN or choline Cl. The application of 50 µmol/l Fe²⁺ at pH 5.5 induced a faster and larger intracellular acidification. These results suggest that DCT1-mediated transport of Fe²⁺ is H⁺ coupled in a symport mechanism. The H⁺ effect was half-maximal at 1.3 µmol/l, and the Hill coefficient for both Fe²⁺ and H⁺ was 1, suggesting a transport stoichiometry of 1:1. DCT1 is a large protein and is predicted to have 12 transmembrane-spanning domains.

A second possible plasma membrane zinc transporter (ZnT-1) has been cloned (Palmiter and Findley 1995 ). This protein is one member of a family of proteins (Palmiter et al. 1996a , 1996b , Huang and Gitschier 1997 ; for a review, see McMahon and Cousins 1998 ) in which the other members of the family are localized to intracellular vesicular membranes. ZnT-1 is a smaller protein than DCT1 and is predicted to have only six transmembrane-spanning domains. Although the expression of ZnT-1 in cultured cells clearly has effects on zinc influx and efflux, it has never been directly demonstrated to transport zinc. The expression of ZnT-1 increased the rate of zinc influx and efflux from cells to the same extent. The efflux of ⁶⁵Zn²⁺ from cells expressing ZnT-1 was increased in a dose-dependent manner by increasing extracellular zinc over a range of 1–50 µmol/l. Extracellular zinc had no effect on the rate of zinc efflux from cells presumably lacking ZnT-1. Various inhibitors (10 mmol/l NaN or KCN) had no effect on zinc influx or efflux. Cd²⁺ (10 µmol/l) and iodoacetate (1 mmol/l) inhibited influx by 35% but had little effect on the rate of zinc efflux. There was no effect of changing the ionic composition of the extracellular media (e.g., K⁺, tetramethylammonium and Na⁺ all gave similar rates of transport; likewise, similar transport rates were obtained in either acetate or Cl^-) on zinc efflux. The removal of Ca²⁺ and Mg²⁺ had no effect on the rate of transport.

	Future studies

TOP ABSTRACT INTRODUCTION Histochemically detectable zinc Future studies REFERENCES

 
To arrive at a complete description of neuronal zinc homeostasis, a better understanding of the various zinc homeostatic mechanisms available to neurons is needed. These studies must include an investigation of the interaction and cellular modulation of the processes involved in zinc homeostasis. Particularly lacking is an adequate understanding of the mechanisms of neuronal plasma membrane transport. There are many important questions related to plasma membrane zinc transport that are at present unanswered. Are there separate zinc influx and efflux transporters, or can a single transporter mediate both influx and efflux? How does plasma membrane transport regulate intracellular zinc content? How are intracellular or extracellular zinc levels sensed, and what second messengers are used? Are cells able to regulate zinc influx and efflux in response to changes in either intracellular or extracellular zinc content or concentrations? Hopefully, future biochemical and genetic studies will provide the answers to these intriguing questions.

Note added in proof:

Recently the molecular cloning and functional expression of a human homolog of the ZRT1 and ZRT2 genes of Saccharomyces cerevisiae have been reported [Gaither, L.A. & Eide, D.J. (2000) Functional expression of the human hZIP2 zinc transporter. J. Biol. Chem. 275: 5560–5564]. When expressed in K562 erythroleukemia cells, the protein was localized to the plasma membrane and demonstrated saturable zinc uptake activity (K_m = 3 µmol/l). Zinc uptake was inhibited when other transition elements were added or when the solution pH was lowered to 5.5.

	FOOTNOTES

 
¹ Presented at the international workshop "Zinc and Health: Current Status and Future Directions," held at the National Institutes of Health in Bethesda, MD, on November 4–5, 1998. This workshop was organized by the Office of Dietary Supplements, NIH and cosponsored with the American Dietetic Association, the American Society for Clinical Nutrition, the Centers for Disease Control and Prevention, Department of Defense, Food and Drug Administration/Center for Food Safety and Applied Nutrition and seven Institutes, Centers and Offices of the NIH (Fogarty International Center, National Institute on Aging, National Institute of Dental and Craniofacial Research, National Institute of Diabetes and Digestive and Kidney Diseases, National Institute on Drug Abuse, National Institute of General Medical Sciences and the Office of Research on Women’s Health). Published as a supplement to The Journal of Nutrition. Guest editors for this publication were Michael Hambidge, University of Colorado Health Sciences Center, Denver; Robert Cousins, University of Florida, Gainesville; Rebecca Costello, Office of Dietary Supplements, NIH, Bethesda, MD; and session chair, Christopher Frederickson, NeuroBio Tex, Inc., Galveston, TX.

² Supported by a grant from the American Heart Association, Mid America Research Consortium.

⁴ Abbreviations used: NMDA, N-methyl-D-aspartate; ZnT, zinc transporter.

	REFERENCES

TOP ABSTRACT INTRODUCTION Histochemically detectable zinc Future studies REFERENCES

 

1. Aniksztein L., Charton G., Ben-Ari Y. Selective release of endogenous zinc from the hippocampal mossy fibers in situ. Brain Res 1987;404:58-64[Medline]

2. Assaf S. Y., Chung S. H. Release of endogenous Zn²⁺ from brain tissue during activity. Nature (Lond.) 1984;308:734-736[Medline]

3. Berger T., Schwarz C., Kraushaar U., Monyer H. Dentate gyrus basket cell GABA_A receptors are blocked by Zn²⁺ via changes of their desensitization kinetics: an in situ patch-clamp and single-cell PCR study. J. Neurosci. 1998;18:2437-2448[Abstract/Free Full Text]

4. Charton G., Rovira C., Ben-Ari Y., Leviel V. Spontaneous and evoked release of endogenous Zn²⁺ in the hippocampal mossy fiber zone of the rat in situ. Exp. Brain Res. 1985;58:202-205[Medline]

5. Chen N., Moshaver A., Raymond L. A. Differential sensitivity of recombinant N-methyl-D-aspartate receptor subtypes to zinc inhibition. Mol. Pharmacol. 1997;51:1015-1023[Abstract/Free Full Text]

6. Choi D. W., Koh J. Y. Zinc and brain injury. Annu. Rev. Neurosci. 1998;21:347-375[Medline]

7. Colvin R. A. Characterization of a plasma membrane zinc transporter in rat brain. Neurosci. Lett. 1998a;247:147-150[Medline]

8. Colvin R. A. Zinc inhibits Ca²⁺ transport by rat brain Na⁺/Ca²⁺ exchanger. Neuroreport 1998b;9:3091-3096[Medline]

9. Colvin R. A., Davis N., Nipper R. W., Carter P. A. Evidence for a zinc/proton antiporter in rat brain. Neurochem. Int. 2000;36:539-547[Medline]

10. Cuajungco M. P., Lees G. J. Zinc metabolism in the brain: relevance to human neurodegenerative disorders. Neurobiol. Dis. 1997;4:137-169[Medline]

11. Erickson J. C., Hollopeter G., Thomas S. A., Froelick G. J., Palmiter R. D. Disruption of the metallothionein-III gene in mice: analysis of brain zinc, behavior, and neuron vulnerability to metals, aging, and seizures. J. Neurosci. 1997;17:1271-1281[Abstract/Free Full Text]

12. Fisher J. L., MacDonald R. L. The role of an subtype M₂-M₃ His in regulating inhibition of GABA_A receptor current by zinc and other divalent cations. J. Neurosci. 1998;18:2944-2953[Abstract/Free Full Text]

13. Fredrickson C. J., Klitenick M. A., Manton W. I., Kirkpatrick J. B. Cytoarchitectonic distribution of zinc in the hippocampus of man and the rat. Brain Res 1983;273:335-339[Medline]

14. Gunshin H., Mackenzie B., Berger U. V., Gunshin Y., Romero M. F., Boron W. F., Nussberger S., Gollan J. L., Hediger M. A. Cloning and characterization of a mammalian proton coupled metal ion transporter. Nature (Lond.) 1997;388:482-488[Medline]

15. Howell G. A., Welch M. G., Frederickson C. J. Stimulation induced uptake and release of zinc in hippocampal slices. Nature (Lond.) 1984;308:736-738[Medline]

16. Huang E. P. Metal ions and synaptic transmission: think zinc. Proc. Natl. Acad. Sci. U.S.A. 1997;94:13386-13387[Free Full Text]

17. Huang L. P., Gitschier J. A novel gene involved in zinc transport is deficient in the lethal milk mouse. Nat. Genet. 1997;17:292-297[Medline]

18. Koh J., Suh S. W., Gwag B. J., He Y. Y., Hsu C. Y., Choi D. W. The role of zinc in selective neuronal death after transient global cerebral ischemia. Science (Washington DC) 1996;272:1013-1016[Abstract]

19. Koh J. Y., Choi D. W. Zinc toxicity on cultured cortical neurons: involvement of N-methyl-D-aspartate receptors. Neuroscience 1994;60:1049-1057[Medline]

20. McMahon R. J., Cousins R. J. Mammalian zinc transporters. J. Nutr. 1998;128:667-670[Abstract/Free Full Text]

21. Norregaard L., Frederiksen D., Nielsen E. O., Gether U. Delineation of an endogenous zinc-binding site in the human dopamine transporter. EMBO J 1998;17:4266-4273[Medline]

22. Palmiter R. D. The elusive functions of metallothioneins. Proc. Natl Acad. Sci. U.S.A. 1998;95:8428-8430[Abstract/Free Full Text]

23. Palmiter R. D., Cole T. B., Findley S. D. ZnT-2 mammalian protein that confers resistance to zinc by facilitating vesicular sequestration. EMBO J 1996a;15:1784-1791[Medline]

24. Palmiter R. D., Cole T. B., Quaife C. J., Findley S. D. ZnT-3, a putative transporter of zinc into synaptic vesicles. Proc. Natl. Acad. Sci. U.S.A. 1996b;93:14934-14939[Abstract/Free Full Text]

25. Palmiter R. D., Findley S. D. Cloning and functional characterization of a mammalian zinc transporter that confers resistance to zinc. EMBO J 1995;14:639-649[Medline]

26. Paoletti P., Ascher P., Neyton J. High-affinity zinc inhibition of NMDA NR1-NR2A receptors. J. Neurosci. 1997;17:5711-5725[Abstract/Free Full Text]

27. Perez-Clausell J., Danscher G. Release of zinc sulphide accumulations into synaptic clefts after in vivo injection of sodium sulphide. Brain Res 1986;362:358-361[Medline]

28. Reyes J. G. Zinc transport in mammalian cells. Am. J. Physiol. 1996;270:C401-C410[Abstract/Free Full Text]

29. Sensi S. L., Canzoniero L.M.T., Yu S. P., Ying H. S., Koh J.-Y., Kerchner G. A., Choi D. W. Measurement of intracellular free zinc in living cortical neurons: routes of entry. J. Neurosci. 1997;17:9554-9564[Abstract/Free Full Text]

30. Traynelis S. F., Burgess M. F., Zheng F., Lyuboslavsky P., Powers J. L. Control of voltage-independent zinc inhibition of NMDA receptors by the NR1 subunit. J. Neurosci. 1998;18:6163-6175[Abstract/Free Full Text]

31. Vandenberg R. J., Mitrovic A. D., Johnston G.A.R. Molecular basis for differential inhibition of glutamate transporter subtypes by zinc ions. Mol. Pharmacol. 1998;54:189-196[Abstract/Free Full Text]

32. Wensink J., Molenaar A. J., Woroniecka U. D., Vandenhammer C.J.A. Zinc uptake into synaptosomes. J. Neurochem. 1988;50:782-789[Medline]

This article has been cited by other articles:

				R. A. Colvin, A. I. Bush, I. Volitakis, C. P. Fontaine, D. Thomas, K. Kikuchi, and W. R. Holmes Insights into Zn2+ homeostasis in neurons from experimental and modeling studies Am J Physiol Cell Physiol, March 1, 2008; 294(3): C726 - C742. [Abstract] [Full Text] [PDF]

				G. Salazar, B. Craige, R. Love, D. Kalman, and V. Faundez Vglut1 and ZnT3 co-targeting mechanisms regulate vesicular zinc stores in PC12 cells J. Cell Sci., May 1, 2005; 118(9): 1911 - 1921. [Abstract] [Full Text] [PDF]

				L. Annunziato, G. Pignataro, and G. F. Di Renzo Pharmacology of Brain Na+/Ca2+ Exchanger: From Molecular Biology to Therapeutic Perspectives Pharmacol. Rev., December 1, 2004; 56(4): 633 - 654. [Abstract] [Full Text] [PDF]

				T. G. Smart, A. M. Hosie, and P. S. Miller Zn2+ Ions: Modulators of Excitatory and Inhibitory Synaptic Activity Neuroscientist, October 1, 2004; 10(5): 432 - 442. [Abstract] [PDF]

				K. Kordas and R. J. Stoltzfus New Evidence of Iron and Zinc Interplay at the Enterocyte and Neural Tissues J. Nutr., June 1, 2004; 134(6): 1295 - 1298. [Abstract] [Full Text] [PDF]

				C. J. Frederickson, W. Maret, and M. P. Cuajungco Zinc and Excitotoxic Brain Injury: A New Model Neuroscientist, February 1, 2004; 10(1): 18 - 25. [Abstract] [PDF]

				C. Klein, R. K. Sunahara, T. Y. Hudson, T. Heyduk, and A. C. Howlett Zinc Inhibition of cAMP Signaling J. Biol. Chem., March 29, 2002; 277(14): 11859 - 11865. [Abstract] [Full Text] [PDF]

				C. J. Frederickson, S. W. Suh, D. Silva, C. J. Frederickson, and R. B. Thompson Importance of Zinc in the Central Nervous System: The Zinc-Containing Neuron J. Nutr., May 1, 2000; 130(5): 1471S - 1483. [Abstract] [Full Text]

				R. A. Colvin pH dependence and compartmentalization of zinc transported across plasma membrane of rat cortical neurons Am J Physiol Cell Physiol, February 1, 2002; 282(2): C317 - C329. [Abstract] [Full Text] [PDF]

This Article Abstract Full Text (PDF) Purchase Article View Shopping Cart Alert me when this article is cited Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via HighWire Citing Articles via Google Scholar Google Scholar Articles by Colvin, R. A. Articles by Carter, P. A. Search for Related Content PubMed PubMed Citation Articles by Colvin, R. A. Articles by Carter, P. A.