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Mammalian Zinc Transport, Trafficking, and Signals

2006; Elsevier BV; Volume: 281; Issue: 34 Linguagem: Inglês

10.1074/jbc.r600011200

1083-351X

Robert J. Cousins, Juan P. Liuzzi, Louis A. Lichten,

Iron Metabolism and Disorders

Structural, catalytic, and regulatory functions of zinc in biology continue to be defined. The number of genes coding for proteins with zinc-binding domains is conservatively estimated at >3% of the human genome but possibly is as much as 10% (1Blasie C.A. Berg J.M. Biochemistry. 2002; 41: 15068-15073Crossref PubMed Scopus (67) Google Scholar, 2Andreini C. Banci L. Bertini I. Rosato A. J. Proteome Res. 2006; 5: 196-201Crossref PubMed Scopus (757) Google Scholar). Zinc utilization in abundant, yet diverse, applications illustrates why organisms have evolved specific pathways to homeostatically regulate availability of this essential micronutrient at specific cellular sites through an array of transporters. Animals regulate zinc gain and loss efficiently. In humans, about 1% of the total body zinc content is replenished daily by the diet (3King J.C. Cousins R.J. Shils M.E. Shike M. Ross A.C. Caballero B. Cousins R.J. Modern Nutrition in Health and Disease. 10th Ed. Lippincott Williams & Wilkins, Baltimore2005: 271-285Google Scholar). This is accomplished principally by tight control of two systems, absorption from the intestine and endogenous loss via pancreatic and other intestinal secretions. Loss-of-function studies have not provided a delineation of how zinc participates in physiologic activities. Nevertheless, immune function and resistance to infection and control of nitrosative and/or oxidative stress of inflammation are two areas of particular contemporary interest. Unfolding knowledge of cell type-specific expression of zinc transporter genes that respond differentially to hormonal and cytokine stimulation should aid in understanding the role of zinc in these physiologic systems. Coordination of intracellular zinc trafficking has focused on the cysteine-rich protein metallothionein (MT). 2The abbreviations used are: MT, metallothionein; ZnT, zinc transporter; TMD, transmembrane domain; IL, interleukin; LZT, LIV-1 subfamily of Zip zinc transporters; STAT, signal transducer and activator of transcription; iNOS, inducible nitric oxide synthase; CDF, cation diffusion facilitator; EMT, epithelial-mesenchymal transition. Zinc-dependent expression of Mt and its well documented response to multiple mediators, including oxidants, cytokines, hormones, and nitric oxide, have been extensively investigated. Here we review recent findings of how zinc transporters and MT influence mammalian cellular zinc metabolism and signaling pathways. The first mammalian zinc transporter gene, ZnT1, was identified in 1995 (4Palmiter R.D. Findley S.D. EMBO J. 1995; 14: 639-649Crossref PubMed Scopus (643) Google Scholar). Before then, zinc transport in animals was viewed as occurring via co-transport as an anionic complex, as an amino acid (cysteine or histidine) chelate, or via the transferrin receptor route (5Ripa S. Ripa R. Minerva Med. 1995; 86: 37-43PubMed Google Scholar, 6Reyes J.G. Am. J. Physiol. 1996; 270: C401-C410Crossref PubMed Google Scholar). Two protein families have now been implicated in zinc transport. The ZnT (solute-linked carrier 30 (SLC30A)) proteins lower intracellular zinc by mediating zinc efflux from cells or influx into intracellular vesicles. The Zip (Zrt- and Irt-like proteins (SLC39A)) proteins promote zinc transport from the extracellular fluid or from intracellular vesicles into the cytoplasm (7Palmiter R.D. Huang L. Eur. J. Physiol. 2004; 447: 744-751Crossref PubMed Scopus (335) Google Scholar, 8Eide D.J. Eur. J. Physiol. 2004; 447: 796-800Crossref PubMed Scopus (304) Google Scholar, 9Liuzzi J.P. Cousins R.J. Annu. Rev. Nutr. 2004; 24: 151-172Crossref PubMed Scopus (473) Google Scholar). The mammalian ZnT family consists of 10 members (ZnT1–10). Zinc transporter activity for most ZnT proteins (ZnT1,2,4–8) has been confirmed indirectly by survival of cells in medium of high zinc content or directly through measuring zinc uptake/efflux or zinc accumulation in transfected or mutated mammalian cells, zinc-sensitive yeast strains, and Xenopus oocytes (4Palmiter R.D. Findley S.D. EMBO J. 1995; 14: 639-649Crossref PubMed Scopus (643) Google Scholar, 10Palmiter R.D. Cole T.B. Findley S.D. EMBO J. 1996; 15: 1784-1791Crossref PubMed Scopus (397) Google Scholar, 11Huang L. Gitschier J. Nat. Genet. 1997; 17: 292-297Crossref PubMed Scopus (310) Google Scholar, 12Kambe T. Narita H. Yamaguchi-Iwai Y. Hirose J. Amano T. Sugiera N. Sasaki R. Mori K. Iwanaga T. Nagao M. J. Biol. Chem. 2002; 277: 19049-19055Abstract Full Text Full Text PDF PubMed Scopus (230) Google Scholar, 13Cragg R.A. Christie G.R. Phillips S.R. Russi R.M. Kury S. Mathers J.C. Taylor P.M. Ford D. J. Biol. Chem. 2002; 277: 22789-22797Abstract Full Text Full Text PDF PubMed Scopus (121) Google Scholar, 14Huang L. Kirschke C.P. Gitschier J. J. Biol. Chem. 2002; 277: 26389-26395Abstract Full Text Full Text PDF PubMed Scopus (178) Google Scholar, 15Kirschke C.P. Huang L. J. Biol. Chem. 2003; 278: 4096-4102Abstract Full Text Full Text PDF PubMed Scopus (228) Google Scholar, 16Chimienti F. Devergnas S. Favier A. Seve M. Diabetes. 2004; 53: 2330-2337Crossref PubMed Scopus (404) Google Scholar). The ZnT-mediated transport mechanism is unknown. Cellular extrusion of zinc and zinc vesicular deposition occur against a zinc concentration gradient; therefore, it is likely that ZnT zinc transporters function as secondary active transporters or perhaps as antiporters. Homologous proteins function as antiporters exchanging Zn2+ for H+ or K+ (17Guffanti A.A. Wei Y. Rood S.V. Krulwich T.A. Mol. Microbiol. 2002; 45: 145-153Crossref PubMed Scopus (111) Google Scholar, 18Chao Y. Fu D. J. Biol. Chem. 2004; 279: 12043-12050Abstract Full Text Full Text PDF PubMed Scopus (122) Google Scholar) or are able to transport zinc without an energy source or proton gradient when reconstituted in proteo-liposomes (19Bloss T. Clemens S. Nies D.H. Planta. 2002; 214: 783-791Crossref PubMed Scopus (87) Google Scholar). There is considerable sequence homology among human ZnT proteins (20Seve M. Chimienti F. Devergnas S. Favier A. BMC Genomics. 2004; 5: 32Crossref PubMed Scopus (119) Google Scholar). These sequences vary in size, and most of them are predicted to have 6 transmembrane domains (TMD) with the exception of ZnT5, which has 12. These proteins have both N and C termini on the cytoplasmic side of the membrane. In addition, most ZnT proteins have a long intracellular loop with a variable number of histidine residues (20Seve M. Chimienti F. Devergnas S. Favier A. BMC Genomics. 2004; 5: 32Crossref PubMed Scopus (119) Google Scholar). These loops should bind zinc and have been implicated as ion-binding domains (21Murgia C. Vespignani I. Cerase J. Nobili F. Perozzi G. Am. J. Physiol. 1999; 277: G1231-G1239PubMed Google Scholar). Hydropathy plots of SLC30 proteins from different species show that four amphipathic TMDs likely form the channel through which zinc is translocated (22Paulsen I.T. Saier Jr., M.H. J. Membr. Biol. 1997; 156: 99-103Crossref PubMed Scopus (297) Google Scholar, 23Lee S.M. Grass G. Haney C.J. Fan B. Rosen B.P. Anton A. Nies D.H. Rensing C. FEMS Microbiol. Lett. 2002; 215: 273-278Crossref PubMed Google Scholar). Some ZnT proteins function as homoor hetero-oligomers (24Suzuki T. Ishihara K. Migaki H. Ishihara K. Nagao M. Yamaguchi-Iwai Y. Kambe T. J. Biol. Chem. 2005; 280: 30956-30962Abstract Full Text Full Text PDF PubMed Scopus (135) Google Scholar). These proteins are purportedly involved in the incorporation of zinc into enzymes, e.g. alkaline phosphatase, by mediating Zn2+ transport into the lumen of the Golgi apparatus (24Suzuki T. Ishihara K. Migaki H. Ishihara K. Nagao M. Yamaguchi-Iwai Y. Kambe T. J. Biol. Chem. 2005; 280: 30956-30962Abstract Full Text Full Text PDF PubMed Scopus (135) Google Scholar). Motifs have been found in ZnT sequences that may allow for protein-protein interactions (21Murgia C. Vespignani I. Cerase J. Nobili F. Perozzi G. Am. J. Physiol. 1999; 277: G1231-G1239PubMed Google Scholar, 25Sim D.L. Chow V.T. Genomics. 1999; 59: 224-233Crossref PubMed Scopus (51) Google Scholar). The mammalian Zip family (SLC39) consists of 14 members. Zinc transport activity for Zip1–8 and 14 has been confirmed (26Gaither L.A. Eide D.J. J. Biol. Chem. 2001; 276: 22258-22264Abstract Full Text Full Text PDF PubMed Scopus (223) Google Scholar, 27Gaither L.A. Eide D.J. J. Biol. Chem. 2000; 275: 5560-5564Abstract Full Text Full Text PDF PubMed Scopus (265) Google Scholar, 28Dufner-Beattie J. Langmade S.J. Wang F. Eide D. Andrews G.K. J. Biol. Chem. 2003; 278: 50142-50150Abstract Full Text Full Text PDF PubMed Scopus (146) Google Scholar, 29Dufner-Beattie J. Wang F. Kuo Y.M. Gitschier J. Eide D. Andrews G.K. J. Biol. Chem. 2003; 278: 33474-33481Abstract Full Text Full Text PDF PubMed Scopus (235) Google Scholar, 30Wang F. Kim B.E. Petris M.J. Eide D.J. J. Biol. Chem. 2004; 279: 51433-51441Abstract Full Text Full Text PDF PubMed Scopus (126) Google Scholar, 31Taylor K.M. Morgan H.E. Johnson A. Nicholson R.I. FEBS Lett. 2005; 579: 427-432Crossref PubMed Scopus (128) Google Scholar, 32Huang L. Kirschke C.P. Zhang Y. Yu Y.Y. J. Biol. Chem. 2005; 280: 15456-15463Abstract Full Text Full Text PDF PubMed Scopus (164) Google Scholar, 33Begum N.A. Kobayashi M. Moriwaki Y. Matsumoto M. Toyoshima K. Seya T. Genomics. 2002; 80: 630-645Crossref PubMed Scopus (119) Google Scholar, 34Liuzzi J.P. Lichten L.A. Rivera S. Blanchard R.K. Aydemir T.B. Knutson M.D. Ganz T. Cousins R.J. Proc. Natl. Acad. Sci. U. S. A. 2005; 102: 6843-6848Crossref PubMed Scopus (445) Google Scholar) by using transfection of DNA into mammalian (human embryonic kidney, K562, and Chinese hamster ovary) cells. Transport activity has been measured by 65Zn uptake or by using probes that produce emission fluorescence upon binding intracellular labile zinc. Cell-permeable fluorophores include Zinquin, Zin-naphthopyr 1, Newport Green, and FluoZin-3AM. Ion specificity and advances in fluorescence output and photostability of these fluorophores have improved their use for zinc trafficking and imaging studies. The mechanism of Zip-mediated transport is not well understood. Zinc uptake could be a facilitated process driven by a concentration gradient. hZip1 and hZip2 transporter activities do not require ATP (26Gaither L.A. Eide D.J. J. Biol. Chem. 2001; 276: 22258-22264Abstract Full Text Full Text PDF PubMed Scopus (223) Google Scholar, 27Gaither L.A. Eide D.J. J. Biol. Chem. 2000; 275: 5560-5564Abstract Full Text Full Text PDF PubMed Scopus (265) Google Scholar). Zip-dependent transport activity is induced by HCO–3, which suggests a symport mechanism (27Gaither L.A. Eide D.J. J. Biol. Chem. 2000; 275: 5560-5564Abstract Full Text Full Text PDF PubMed Scopus (265) Google Scholar). Metal competition studies indicate some mammalian Zip proteins are specific for zinc (28Dufner-Beattie J. Langmade S.J. Wang F. Eide D. Andrews G.K. J. Biol. Chem. 2003; 278: 50142-50150Abstract Full Text Full Text PDF PubMed Scopus (146) Google Scholar, 29Dufner-Beattie J. Wang F. Kuo Y.M. Gitschier J. Eide D. Andrews G.K. J. Biol. Chem. 2003; 278: 33474-33481Abstract Full Text Full Text PDF PubMed Scopus (235) Google Scholar, 30Wang F. Kim B.E. Petris M.J. Eide D.J. J. Biol. Chem. 2004; 279: 51433-51441Abstract Full Text Full Text PDF PubMed Scopus (126) Google Scholar); however, zinc uptake activity for h/mZip1, mZip3, and hZip2 was found to be inhibited by multiple cations (26Gaither L.A. Eide D.J. J. Biol. Chem. 2001; 276: 22258-22264Abstract Full Text Full Text PDF PubMed Scopus (223) Google Scholar, 27Gaither L.A. Eide D.J. J. Biol. Chem. 2000; 275: 5560-5564Abstract Full Text Full Text PDF PubMed Scopus (265) Google Scholar, 28Dufner-Beattie J. Langmade S.J. Wang F. Eide D. Andrews G.K. J. Biol. Chem. 2003; 278: 50142-50150Abstract Full Text Full Text PDF PubMed Scopus (146) Google Scholar). Recently, the transport activity of Zip14 for both zinc and non-transferrin-bound iron, when overexpressed in HEK cells and Sf9 insect cells, has been demonstrated. 3J. P. Liuzzi, F. Aydemir, H. Nam, M. D. Knutson, and R. J. Cousins, unpublished observations. A dendogram shows sequence similarity among mouse Zip proteins (supplemental Fig. 1). The Zip family can be divided into four subfamilies: Zip I, Zip II, gufA, and LZT (35Taylor K.M. Nicholson R.I. Biochim. Biophys. Acta. 2003; 1611: 16-30Crossref PubMed Scopus (215) Google Scholar). Most mammalian Zip proteins, including Zip4–8, Zip10, and Zip12–14, belong to the LZT subfamily. Zip1–3 are from the Zip II subfamily; Zip9 is from the Zip I subfamily; and Zip11 clusters within the gufA subfamily. The LZT transporter family was named after LIV-1 (Zip6), the first Zip member (36Taylor K.M. IUBMB Life. 2000; 49: 249-253Crossref PubMed Scopus (37) Google Scholar). Most Zip proteins are predicted to have eight TMDs, but LIV-1 has only six. TMDs IV and V are highly conserved and could form the pore through which metals pass (37Rogers E.E. Eide D.J. Guerinot M.L. Proc. Natl. Acad. Sci. U. S. A. 2000; 97: 12356-12360Crossref PubMed Scopus (375) Google Scholar, 38Gaither L.A. Eide D.J. Biometals. 2001; 14: 251-270Crossref PubMed Scopus (433) Google Scholar). Zip proteins are predicted to have extracellular N and C termini and a long intracellular loop with a histidine-rich repeat (35Taylor K.M. Nicholson R.I. Biochim. Biophys. Acta. 2003; 1611: 16-30Crossref PubMed Scopus (215) Google Scholar). In contrast, immunolocalization studies suggest mouse Zip14 has an extracellular histidine-rich loop (34Liuzzi J.P. Lichten L.A. Rivera S. Blanchard R.K. Aydemir T.B. Knutson M.D. Ganz T. Cousins R.J. Proc. Natl. Acad. Sci. U. S. A. 2005; 102: 6843-6848Crossref PubMed Scopus (445) Google Scholar). The presence of specific motifs may confer to Zip proteins the option of other functions separate from zinc transport or for protein-protein interactions involving zinc. For example, the novel metalloprotease motif (HEXPHEXGD) of LZT proteins may allow them to function as matrix metalloproteases or participate in the catalytic properties of these enzymes. Zip10 has putative C2H2 zinc finger and cytochrome c motifs in its first TMD, suggesting novel roles for targeted metal transport. Most ZnT proteins have been found in intracellular compartments, usually associated with endosomes, Golgi, or endoplasmic reticulum. ZnT1 appears to be the only ZnT transporter located at the plasma membrane, congruent with its role as the primary regulator of cellular zinc efflux (4Palmiter R.D. Findley S.D. EMBO J. 1995; 14: 639-649Crossref PubMed Scopus (643) Google Scholar). ZnT2 has a vesicular localization in pancreatic acinar cells, whereas ZnT1 has a vesicular localization but is also at the plasma membrane (39Liuzzi J.P. Bobo J.A. Lichten L.A. Samuelson D.A. Cousins R.J. Proc. Natl. Acad. Sci. U. S. A. 2004; 101: 14355-14360Crossref PubMed Scopus (155) Google Scholar). ZnT9 is located in the nucleus during mitosis (25Sim D.L. Chow V.T. Genomics. 1999; 59: 224-233Crossref PubMed Scopus (51) Google Scholar). ZnT5 localizes with secretory vesicles of pancreatic β cells and at the apical membrane of enterocytes. ZnT10 could be located at the plasma membrane according to software calculations. Most Zip proteins have been observed at the plasma membrane; however, Zip7 was located at the Golgi apparatus (32Huang L. Kirschke C.P. Zhang Y. Yu Y.Y. J. Biol. Chem. 2005; 280: 15456-15463Abstract Full Text Full Text PDF PubMed Scopus (164) Google Scholar). The localization of some Zip transporters may change according to zinc availability or physiologic conditions. Zip5 has a basolateral plasma membrane orientation in polarized cells during dietary zinc sufficiency, but its regulation by zinc is not defined (30Wang F. Kim B.E. Petris M.J. Eide D.J. J. Biol. Chem. 2004; 279: 51433-51441Abstract Full Text Full Text PDF PubMed Scopus (126) Google Scholar, 40Dufner-Beattie J. Kuo Y.M. Gitschier J. Andrews G.K. J. Biol. Chem. 2004; 279: 49082-49090Abstract Full Text Full Text PDF PubMed Scopus (182) Google Scholar). Similarly, Zip14 is mobilized to the sinusoidal membrane of the mouse hepatocyte during acute inflammation and, therefore, increases zinc uptake as a component of the acute phase response. Studies where zinc transporter regulation has been examined within an integrative context merge well with known zinc physiology (Fig. 1). The positive mode of ZnT1 regulation by zinc supports regulation by MTF1 (metal-responsive transcription factor 1). ZnT1 was identified as the gene responsible for zinc resistance in mutated baby hamster kidney cells and genomic ZnT1 sequences (4Palmiter R.D. Findley S.D. EMBO J. 1995; 14: 639-649Crossref PubMed Scopus (643) Google Scholar). The behavior of ZnT1 and a metal-responsive element-β Geo reporter gene to zinc concentrations was similar. Homozygous knock-outs of either ZnT1 or MTF1 in mice are lethal to the embryo (41Langmade S.J. Ravindra R. Daniels P.J. Andrews G.K. J. Biol. Chem. 2000; 275: 34803-34809Abstract Full Text Full Text PDF PubMed Scopus (319) Google Scholar). Homozygous MTF1–/– embryos do not express any ZnT1 mRNA compared with those from wild-type or heterozygous mice, suggesting ZnT1 is MTF1-regulated. In rodents, ZnT1 is ubiquitously expressed, but mRNA abundance exhibits wide differences among tissues (7Palmiter R.D. Huang L. Eur. J. Physiol. 2004; 447: 744-751Crossref PubMed Scopus (335) Google Scholar, 9Liuzzi J.P. Cousins R.J. Annu. Rev. Nutr. 2004; 24: 151-172Crossref PubMed Scopus (473) Google Scholar). The response of ZnT1 to dietary zinc restriction or supplementation is also variable among different tissues (41Langmade S.J. Ravindra R. Daniels P.J. Andrews G.K. J. Biol. Chem. 2000; 275: 34803-34809Abstract Full Text Full Text PDF PubMed Scopus (319) Google Scholar, 42Liuzzi J.P. Blanchard R.K. Cousins R.J. J. Nutr. 2001; 131: 46-52Crossref PubMed Scopus (203) Google Scholar, 43McMahon R.J. Cousins R.J. Proc. Natl. Acad. Sci. U. S. A. 1998; 95: 4841-4846Crossref PubMed Scopus (257) Google Scholar). ZnT1 transcript levels are markedly reduced in peripheral blood mononuclear cells of zinc-deficient mice (39Liuzzi J.P. Bobo J.A. Lichten L.A. Samuelson D.A. Cousins R.J. Proc. Natl. Acad. Sci. U. S. A. 2004; 101: 14355-14360Crossref PubMed Scopus (155) Google Scholar). In humans, ZnT1 mRNA levels in leukocytes increase markedly upon dietary zinc supplementation (44Aydemir T.B. Blanchard R.K. Cousins R.J. Proc. Natl. Acad. Sci. U. S. A. 2006; 103: 1699-1704Crossref PubMed Scopus (129) Google Scholar). Among human leukocyte subsets, ZnT1 transcripts are more abundant in monocytes than T-lymphocytes or neutrophils. Zinc responsiveness of ZnT1 is not dependent upon MT expression as it is normal in MT–/– mice (45Davis S.R. McMahon R.J. Cousins R.J. J. Nutr. 1998; 128: 825-831Crossref PubMed Scopus (81) Google Scholar). Expression of neuronal ZnT1 is induced by forebrain ischemia (46Tsuda M. Imaizumi K. Katayama T. Kitagawa K. Wanaka A. Tohyama M. Takagi T. J. Neurosci. 1997; 17: 6678-6684Crossref PubMed Google Scholar), and considerable evidence shows ZnT1 is protective against Zn2+-induced neuronal cell damage by promoting efflux (47Kim A.H. Sheline C.T. Tian M. Higashi T. McMahon R.J. Cousins R.J. Choi D.W. Brain Res. 2000; 886: 99-107Crossref PubMed Scopus (96) Google Scholar, 48Nolte C. Gore A. Sekler I. Kresse W. Hershfinkel M. Hoffmann A. Kettenmann H. Moran A. Glia. 2004; 48: 145-155Crossref PubMed Scopus (90) Google Scholar). Multiple mutations in human Zip4 produce the zinc malabsorption phenotype, acrodermatitis enteropathica (49Wang K. Zhou B. Kuo Y.M. Zemansky J. Gitschier J. Am. J. Hum. Genet. 2002; 71: 66-73Abstract Full Text Full Text PDF PubMed Scopus (400) Google Scholar). Dietary zinc restriction in mice up-regulates Zip4 and causes an increase in Zip4 localized to the plasma membrane of enterocytes (29Dufner-Beattie J. Wang F. Kuo Y.M. Gitschier J. Eide D. Andrews G.K. J. Biol. Chem. 2003; 278: 33474-33481Abstract Full Text Full Text PDF PubMed Scopus (235) Google Scholar, 39Liuzzi J.P. Bobo J.A. Lichten L.A. Samuelson D.A. Cousins R.J. Proc. Natl. Acad. Sci. U. S. A. 2004; 101: 14355-14360Crossref PubMed Scopus (155) Google Scholar). Repletion with zinc rapidly down-regulates Zip4 expression and lowers membrane localization to basal conditions (39Liuzzi J.P. Bobo J.A. Lichten L.A. Samuelson D.A. Cousins R.J. Proc. Natl. Acad. Sci. U. S. A. 2004; 101: 14355-14360Crossref PubMed Scopus (155) Google Scholar). Presumably, individuals with acrodermatitis enteropathica do not synthesize a fully functional Zip4 and are not capable of transporting sufficient dietary zinc to prevent a systemic deficiency. The defect can be overridden with supplemental dietary zinc. Therefore, supplemental zinc is used as a therapeutic measure (3King J.C. Cousins R.J. Shils M.E. Shike M. Ross A.C. Caballero B. Cousins R.J. Modern Nutrition in Health and Disease. 10th Ed. Lippincott Williams & Wilkins, Baltimore2005: 271-285Google Scholar). The mechanism of the negative responsiveness of Zip4 to zinc is not known. Up-regulation of Zip4 in enterocytes and concurrent down-regulation of ZnT1 and ZnT2 in pancreatic acinar cells of mice when dietary zinc intake is low are key factors that may balance intestinal intake with endogenous loss via pancreatic secretions (homeostasis) (39Liuzzi J.P. Bobo J.A. Lichten L.A. Samuelson D.A. Cousins R.J. Proc. Natl. Acad. Sci. U. S. A. 2004; 101: 14355-14360Crossref PubMed Scopus (155) Google Scholar). Additionally, it has been proposed that Zip 5, although constitutively expressed in intestine and pancreatic acinar cells, is differentially internalized in response to dietary zinc intake and thus contributes to integrative homeostasis through producing less plasma to cell zinc transport in intestine (40Dufner-Beattie J. Kuo Y.M. Gitschier J. Andrews G.K. J. Biol. Chem. 2004; 279: 49082-49090Abstract Full Text Full Text PDF PubMed Scopus (182) Google Scholar) and kidney (30Wang F. Kim B.E. Petris M.J. Eide D.J. J. Biol. Chem. 2004; 279: 51433-51441Abstract Full Text Full Text PDF PubMed Scopus (126) Google Scholar). Mtf1–/– liver cells show up-regulation of Zip10, suggesting MTF1 represses expression under basal conditions (50Wimmer U. Wang Y. Georgiev O. Schaffner W. Nucleic Acids Res. 2005; 33: 5715-5727Crossref PubMed Scopus (130) Google Scholar). The up-regulation of Zip4 during zinc deficiency may be another example of MTF1 negative regulation (29Dufner-Beattie J. Wang F. Kuo Y.M. Gitschier J. Eide D. Andrews G.K. J. Biol. Chem. 2003; 278: 33474-33481Abstract Full Text Full Text PDF PubMed Scopus (235) Google Scholar, 39Liuzzi J.P. Bobo J.A. Lichten L.A. Samuelson D.A. Cousins R.J. Proc. Natl. Acad. Sci. U. S. A. 2004; 101: 14355-14360Crossref PubMed Scopus (155) Google Scholar). Similarly, monocytic human cell lines made zinc deficient using a cell-permeant Zn2+ chelator show increased Zip2 expression (51Cousins R.J. Blanchard R.K. Popp M.P. Liu L. Cao J. Moore J.B. Green C.L. Proc. Natl. Acad. Sci. U. S. A. 2003; 100: 6952-6957Crossref PubMed Scopus (153) Google Scholar). A corresponding increase in expression of a putative, uncharacterized, zinc-responsive transcription factor MTF2 was observed. Of note is that in zinc-supplemented human subjects, ZnT1 and Mt expression, both of which are MTF1 mediated, are increased, although Zip3 expression is decreased under the same conditions (44Aydemir T.B. Blanchard R.K. Cousins R.J. Proc. Natl. Acad. Sci. U. S. A. 2006; 103: 1699-1704Crossref PubMed Scopus (129) Google Scholar). Findings that some Zip genes are down-regulated by zinc is of considerable interest, as it is indicative of another potential mode of regulation by zinc. A number of ZnT/Zip transporter genes appear to be regulated by hormones or cytokines (Fig. 2). These relationships closely follow established roles of these mediators in zinc physiology. Developmentally regulated changes in expression of some ZnT genes have been reported (9Liuzzi J.P. Cousins R.J. Annu. Rev. Nutr. 2004; 24: 151-172Crossref PubMed Scopus (473) Google Scholar). Zip1 in prostate is regulated by prolactin and testosterone and may contribute to the atypically high zinc in the prostatic epithelium (52Franklin R.B. Feng P. Milon B. Desouki M.M. Singh K.K. Kajdacsy-Balla A. Bagasra O. Costello L.C. Mol. Cancer. 2005; 4: 32Crossref PubMed Scopus (192) Google Scholar). Zip1 is markedly reduced in the malignant prostate and correlates with concomitantly lower zinc concentration in the malignant cells. Zip3 expression is very high in mammary epithelial cells, is inducible with prolactin, and is correlated with 65Zn transport as shown by knockdown with small interfering RNA (53Kelleher S.L. Lonnerdal B. Am. J. Physiol. 2005; 288: C1042-C1047Crossref PubMed Scopus (66) Google Scholar). LIV1 (Zip6) was identified as a novel estrogen-responsive gene in breast cancer cells that sequence data revealed was a member of the Zip transporter family (36Taylor K.M. IUBMB Life. 2000; 49: 249-253Crossref PubMed Scopus (37) Google Scholar). Zip6 expression is related to metastasis to lymph nodes. cDNA transfection and Newport Green (Zn2+ fluorophore) were used to demonstrate Zip6 transporter function. Zip8 (BIGM103) was identified as a TNFαand endotoxin-induced gene expressed in monocytes (33Begum N.A. Kobayashi M. Moriwaki Y. Matsumoto M. Toyoshima K. Seya T. Genomics. 2002; 80: 630-645Crossref PubMed Scopus (119) Google Scholar). Expression is very low in unstimulated monocytes. DNA microarray analysis of the response of humans to acute systemic inflammation induced by endotoxin administration revealed a marked transient increase in Zip8 expression in total leukocytic RNA. 4R. J. Cousins and T. Beker Aydemir, unpublished results. Among human leukocytes, Zip8 exhibits extremely high transcript abundance in T-lymphocytes (44Aydemir T.B. Blanchard R.K. Cousins R.J. Proc. Natl. Acad. Sci. U. S. A. 2006; 103: 1699-1704Crossref PubMed Scopus (129) Google Scholar). Systemic responses to sepsis and inflammation include hepatic zinc uptake, which produces a transient hypozincemia (3King J.C. Cousins R.J. Shils M.E. Shike M. Ross A.C. Caballero B. Cousins R.J. Modern Nutrition in Health and Disease. 10th Ed. Lippincott Williams & Wilkins, Baltimore2005: 271-285Google Scholar). Zip14 was identified as highly induced in hepatocytes of mice during the acute phase response (34Liuzzi J.P. Lichten L.A. Rivera S. Blanchard R.K. Aydemir T.B. Knutson M.D. Ganz T. Cousins R.J. Proc. Natl. Acad. Sci. U. S. A. 2005; 102: 6843-6848Crossref PubMed Scopus (445) Google Scholar). This novel Zip protein was demonstrated to transport zinc (31Taylor K.M. Morgan H.E. Johnson A. Nicholson R.I. FEBS Lett. 2005; 579: 427-432Crossref PubMed Scopus (128) Google Scholar, 34Liuzzi J.P. Lichten L.A. Rivera S. Blanchard R.K. Aydemir T.B. Knutson M.D. Ganz T. Cousins R.J. Proc. Natl. Acad. Sci. U. S. A. 2005; 102: 6843-6848Crossref PubMed Scopus (445) Google Scholar). Wild-type mice produce robust amounts of Zip14 mRNA in response to acute inflammation and exhibit hypozincemia, whereas IL6–/– mice produce no Zip14 and do not experience hypozincemia. Inflammation and IL6 in vitro increase Zip14 at the plasma membrane of hepatocytes. A probable signal pathway for this IL6-mediated response is via STAT regulation. Zip14 regulation by lipopolysaccharide during the acute phase is more complex, including NO-induced activation of AP-1. 5L. A. Lichten and R. J. Cousins, unpublished results. Zip14 regulation by IL6 and NO has implications for a role of zinc in resistance to toxin-induced liver injury and cancer progression. Physiologic stimuli that regulate metallothionein synthesis merge with those that regulate specific ZnT and Zip genes (Fig. 2). Expression of MT is ubiquitous but is particularly high in parenchymal cells of the intestine, pancreas, kidney, and liver. Spatial arrangement of the 20 cysteines of the MT molecule accounts for metal binding that has high thermodynamic and high kinetic lability (54Zangger K. Oz G. Haslinger E. Kunert O. Armitage I.M. FASEB J. 2001; 15: 1303-1305Crossref PubMed Scopus (108) Google Scholar). The β domain binds three Zn2+ atoms via thiolate ligands from nine cysteines. The α domain binds four Zn2+ atoms via eleven cysteines. The metabolic pool from which the apo-MT (thionein) molecule acquires these seven Zn2+ atoms has not been identified. Structural studies using 1Hand 113Cd-NMR spectroscopy reveal that Zn2+ atoms bound to thiolates of the β domain are more labile than those of the α domain (54Zangger K. Oz G. Haslinger E. Kunert O. Armitage I.M. FASEB J. 2001; 15: 1303-1305Crossref PubMed Scopus (108) Google Scholar). This suggests the β domain is physiologically relevant, whereas the α domain may be related to metal detoxification. Such dual properties for the same molecule complicate interpretation of studies aimed at function. MT binds Zn2+ strongly (up to 1013m–1). However, experiments using model systems suggest MT may assume a donor/acceptor role for zinc-binding motifs and could activate or deactivate apozinc finger proteins or other zinc metalloproteins (55Roesijadi G. Bogumil R. Vasak M. Kaki J.H. J. Biol. Chem. 1998; 273: 17425-17432Abstract Full Text Full Text PDF PubMed Scopus (90) Google Scholar). Viability of MT–/– mice suggests essential zinc-dependent functions, such as formation of zinc finger proteins, acquire zinc from sources other than MT. A widely studied role of MT is its ability to protect in vivo and in vitro against cellular stressors such as carbon-centered radicals and reactive oxygen and nitrogen species. The mechanism of cytoprotection remains unclear. In vitro studies have shown that the metal thiolate clusters of MT possess the unique ability to function as a redox unit; therefore, the protein has the potential to be involved in redox-sensitive signaling pathways (56Maret W. Biochemistry. 2004; 43: 3301-3309Crossref PubMed Scopus (230) Google Scholar). Comparative studies with nitric oxide (NO), H2O2, singlet oxygen, peroxyl radicals, and peroxynitrite suggest only stress from NO causing S-nitrosylation of MT cysteines and Zn2+ release is sufficiently mild to allow reconstitution of MT through Zn2+ rebinding (57Kröncke K.D. Klotz L.O. Suschek C.V. Sies H. J. Biol. Chem. 2002; 277: 13294-13301Abstract Full Text Full Text PDF PubMed Scopus (61) Google Scholar). Fluorescence resonance energy transfer experiments have confirmed that in cultured endothelial cells MT undergoes conformational changes in the presence of NO donors, e.g. S-nitrocysteine (58St. Croix C.M. Stitt M.S. Leelavanichkul K. Wasserloos K.J. Pitt B.R. Watkins S.C. Free Radic. Biol. Med. 2004; 37: 785-792Crossref PubMed Scopus (25) Google Scholar). These alterations in cellular zinc homeostasis suggest protective effects of MT against nitric oxide toxicity (54Zangger K. Oz G. Haslinger E. Kunert O. Armitage I.M. FASEB J. 2001; 15: 1303-1305Crossref PubMed Scopus (108) Google Scholar). During inflammation or endotoxemia, hepatocytes respond to cytokines by up-regulating inducible nitric oxide synthase (iNOS), which generates large amounts of NO from arginine. Increased MT expression parallels the rise in cellular NO (59Spahl D.U. Berendji-Grun D. Suschek C.V. Kolb-Bachofen V. Kröncke K.D. Proc. Natl. Acad. Sci. U. S. A. 2003; 100: 13952-13957Crossref PubMed Scopus (140) Google Scholar). NO promotes zinc release from MT, which in turn may repress iNOS (54Zangger K. Oz G. Haslinger E. Kunert O. Armitage I.M. FASEB J. 2001; 15: 1303-1305Crossref PubMed Scopus (108) Google Scholar). In zinc-deficient rodents, iNOS expression increases (60Cui L. Blanchard R.K. Cousins R.J. J. Nutr. 2003; 133: 51-56Crossref PubMed Scopus (17) Google Scholar), perhaps because MT-bound zinc is not available. Another link between NO and MT may be through MTF1 activation. MTF1 nuclear translocation occurs under a variety of stress conditions. Hypoxia and oxidants such as H2O2 and tert-butylhydroquinone have been shown to increase MTF1 binding to the metal-responsive elements of the MT promoter. Release of labile zinc from MT or other thiolate ligands by NO may provide the means, via zinc binding to MTF1 and other zinc finger proteins, for regulation of other metal-responsive genes that are involved in cellular protection, including those of the ZnT and Zip families. Homology between mammalian and non-mammalian zinc transporters suggests conserved functions. Here we present two examples, drawn from the non-mammalian literature, that integrate zinc transport into cell signaling mechanisms common to divergent species, including mammals (Fig. 2). Zinc has been shown to inhibit Ras signaling in numerous in vitro experiments. In Caenorhabditis elegans, the cation diffusion facilitator (CDF) protein family confers resistance to many heavy metals. CDF-1, which is a homologue of mammalian ZnT1, responds to Zn2+ in a mode consistent with activity as a zinc exporter (61Bruinsma J.J. Jirakulaporn T. Muslin A.J. Kornfeld K. Dev. Cell. 2002; 2: 567-578Abstract Full Text Full Text PDF PubMed Scopus (103) Google Scholar). CDF-1 activity reduces cytosolic Zn2+ concentrations and concomitantly increases Ras-mediated signaling. Zn2+ may function to maintain Ras in an inactive state. Because CDF-1 is expressed in intestinal cells of C. elegans, there is a potential for ZnT1 involvement in the abnormal regulation of Ras associated with colon cancer in humans. Similarly, CDF-1 and ZnT1 bind to Raf-1 and may be responsible for full activation of this downstream component of transduction (62Jirakulaporn T. Muslin A.J. J. Biol. Chem. 2004; 279: 27807-27815Abstract Full Text Full Text PDF PubMed Scopus (57) Google Scholar) initiated through ligand binding by receptors for growth factors, mitogens, and hormones. Zip6 (LIV1) may be involved in control of epithelial-mesenchymal transition (EMT). EMT is essential for embryonic development, tissue regeneration, and metastasis of neoplastic cells. During gastrulation in zebrafish, STAT3-dependent zLIV-1 (Zip6) expression regulates the nuclear translocation of the zinc finger protein Snail, which regulates EMT in organizer cells, and their invasive behavior (63Yamashita S. Miyagi C. Fukada T. Kagara N. Che Y.S. Hirano T. Nature. 2004; 429: 298-302Crossref PubMed Scopus (318) Google Scholar). Through comparable mechanisms, Zip6 and Snail may be involved in metastasis of breast cancer cells, possibly through constitutive activation by STAT3 (64Taylor K.M. Hiscox S. Nicholson R.I. Trends Endocrinol. Metab. 2004; 15: 461-463Abstract Full Text Full Text PDF PubMed Scopus (56) Google Scholar). Similarly, the LIV1 (Zip6) homologue FOI, the fear of intimacy gene, is required for proper gonad formation in Drosophila (65Mathews W.R. Ong D. Milutinovich A.B. Van Doren M. Development. 2006; 133: 1143-1153Crossref PubMed Scopus (48) Google Scholar). A common downstream target for LIV1 (Zip6) and its homologues could be to inactivate cadherin expression, which has important roles in development, tissue remodeling, wound healing, and tumor promotion and metastasis. Within the past decade, tremendous strides have been made toward our understanding of zinc transport. Evolving descriptions of tissue-specific expression and regulation by zinc through metal-responsive transcription factor, MTF1, or through cytokines, growth factors, and hormones merge well with known zinc physiology. The emerging role of Zn2+ as another secondary signaling mediator and control of that signaling through cellular and vesicular transport is providing exciting new insights into functional outcomes of zinc trafficking. Pathways of Zn2+ transport and their dysregulation have been linked to specific diseases. The labile nature of Zn2+ bound to specific zinc finger motifs and in cluster domains, as found in metallothionein, has shown how nitric oxide and reactive oxygen species mobilize bound Zn2+ with subsequent reentry into cellular Zn2+ pools.