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• W2039813168 abstract "Vesicular glutamate transporter is present in neuronal synaptic vesicles and endocrine synaptic-like microvesicles and is responsible for vesicular storage ofl-glutamate. A brain-specific Na+-dependent inorganic phosphate transporter (BNPI) functions as a vesicular glutamate transporter in synaptic vesicles, and the expression of this BNPI defines the glutamatergic phenotype in the central nervous system (Bellocchio, E. E., Reimer, R. J., Fremeau, R. T., Jr., and Edwards, R. H. (2000) Science 289, 957–960; Takamori, S., Rhee, J. S., Rosenmund, C., and Jahn, R. (2000) Nature 407, 189–194). However, since not all glutamatergic neurons contain BNPI, an additional transporter(s) responsible for vesicular glutamate uptake has been postulated. Here we report that differentiation-associated Na+-dependent inorganic phosphate cotransporter (DNPI), an isoform of BNPI (Aihara, Y., Mashima, H., Onda, H., Hisano, S., Kasuya, H., Hori, T., Yamada, S., Tomura, H., Yamada, Y., Inoue, I., Kojima, I., and Takeda, J. (2000) J. Neurochem.74, 2622–2625), also transports l-glutamate at the expense of an electrochemical gradient of protons established by the vacuolar proton pump when expressed in COS7 cells. Molecular, biological, and immunohistochemical studies have indicated that besides its presence in neuronal cells DNPI is preferentially expressed in mammalian pinealocytes, αTC6 cells, clonal pancreatic α cells, and α cells of Langerhans islets, these cells being proven to secretel-glutamate through Ca2+-dependent regulated exocytosis followed by its vesicular storage. Pancreatic polypeptide-secreting F cells of Langerhans islets also expressed DNPI. These results constitute evidence that DNPI functions as another vesicular transporter in glutamatergic endocrine cells as well as in neurons. Vesicular glutamate transporter is present in neuronal synaptic vesicles and endocrine synaptic-like microvesicles and is responsible for vesicular storage ofl-glutamate. A brain-specific Na+-dependent inorganic phosphate transporter (BNPI) functions as a vesicular glutamate transporter in synaptic vesicles, and the expression of this BNPI defines the glutamatergic phenotype in the central nervous system (Bellocchio, E. E., Reimer, R. J., Fremeau, R. T., Jr., and Edwards, R. H. (2000) Science 289, 957–960; Takamori, S., Rhee, J. S., Rosenmund, C., and Jahn, R. (2000) Nature 407, 189–194). However, since not all glutamatergic neurons contain BNPI, an additional transporter(s) responsible for vesicular glutamate uptake has been postulated. Here we report that differentiation-associated Na+-dependent inorganic phosphate cotransporter (DNPI), an isoform of BNPI (Aihara, Y., Mashima, H., Onda, H., Hisano, S., Kasuya, H., Hori, T., Yamada, S., Tomura, H., Yamada, Y., Inoue, I., Kojima, I., and Takeda, J. (2000) J. Neurochem.74, 2622–2625), also transports l-glutamate at the expense of an electrochemical gradient of protons established by the vacuolar proton pump when expressed in COS7 cells. Molecular, biological, and immunohistochemical studies have indicated that besides its presence in neuronal cells DNPI is preferentially expressed in mammalian pinealocytes, αTC6 cells, clonal pancreatic α cells, and α cells of Langerhans islets, these cells being proven to secretel-glutamate through Ca2+-dependent regulated exocytosis followed by its vesicular storage. Pancreatic polypeptide-secreting F cells of Langerhans islets also expressed DNPI. These results constitute evidence that DNPI functions as another vesicular transporter in glutamatergic endocrine cells as well as in neurons. brain-specific Na+-dependent inorganic phosphate cotransporter differentiation-associated Na+-dependent inorganic phosphate cotransporter 3-N-morpholinopropanesulfonic acid synaptic-like microvesicle reverse transcription polymerase chain reaction l-Glutamate is the major excitatory neurotransmitter in the mammalian central nervous system and plays important roles in many neuronal processes such as fast synaptic transmission and neuronal plasticity (1Foster A. Fagg G. Brain Res. 1984; 319: 103-164Crossref PubMed Scopus (673) Google Scholar, 2Mayer M.L. Westbrook G. Prog. Neurobiol. 1997; 28: 197-276Crossref Scopus (1341) Google Scholar). To use l-glutamate as an intercellular signaling molecule, neuronal cells develop glutamatergic systems comprising the storage of glutamate in synaptic vesicles and its exocytosis (signal output), glutamate receptors (signal input), and glutamate reuptake systems (signal termination). Recent evidence has indicated that peripheral endocrine cells also develop glutamatergic systems (3Moriyama Y. Yamamoto A. Yamada H. Tashiro Y. Futa M. Biol. Chem. 1996; 377: 155-165PubMed Google Scholar, 4Moriyama Y. Hayashi M. Yamada H. Yatsushiro S. Ishio S. Yamamoto A. J. Exp. Biol. 2000; 203: 117-125PubMed Google Scholar). For instance, mammalian pinealocytes, endocrine cells for melatonin, secrete l-glutamate through Ca2+-dependent regulated exocytosis and use it as a paracrine- or autocrine-like chemical transmitter to inhibit melatonin synthesis (3Moriyama Y. Yamamoto A. Yamada H. Tashiro Y. Futa M. Biol. Chem. 1996; 377: 155-165PubMed Google Scholar, 4Moriyama Y. Hayashi M. Yamada H. Yatsushiro S. Ishio S. Yamamoto A. J. Exp. Biol. 2000; 203: 117-125PubMed Google Scholar). Vesicular glutamate transporter plays its primary role in the storage of l-glutamate in neurons (5Liu Y. Edwards R.H. Annu. Rev. Neurosci. 1997; 20: 125-156Crossref PubMed Scopus (236) Google Scholar, 6Maycox P.R. Hell J.W. Jahn R. Trends Neurosci. 1990; 13: 83-87Abstract Full Text PDF PubMed Scopus (195) Google Scholar) and endocrine cells (3Moriyama Y. Yamamoto A. Yamada H. Tashiro Y. Futa M. Biol. Chem. 1996; 377: 155-165PubMed Google Scholar, 4Moriyama Y. Hayashi M. Yamada H. Yatsushiro S. Ishio S. Yamamoto A. J. Exp. Biol. 2000; 203: 117-125PubMed Google Scholar) through the transport of l-glutamate at the expense of an electrochemical gradient of protons that is established by vacuolar H+-ATPase. Although vesicular glutamate transporter has been characterized to some extent, its protein nature has not been known long. Very recently brain-specific Na+-dependent inorganic phosphate cotransporter (BNPI),1 representing a family of proteins that use the inwardly directed Na+gradient across the membrane and transport inorganic phosphate (7Ni B. Rosteck Jr., P.R. Nadi N.S. Paul S.M. Proc. Natl. Acad. Sci. U. S. A. 1994; 91: 5607-5611Crossref PubMed Scopus (274) Google Scholar), has been identified as the vesicular glutamate transporter in synaptic vesicles (8Bellocchio E.E. Reimer R.J. Fremeau Jr., R.T. Edwards R.H. Science. 2000; 289: 957-960Crossref PubMed Scopus (657) Google Scholar, 9Takamori S. Rhee J.S. Rosenmund C. Jahn R. Nature. 2000; 407: 189-194Crossref PubMed Scopus (705) Google Scholar). Upon expression in either PC12 or BON6 cells, BNPI becomes associated with secretory vesicles and accumulatesl-glutamate (8Bellocchio E.E. Reimer R.J. Fremeau Jr., R.T. Edwards R.H. Science. 2000; 289: 957-960Crossref PubMed Scopus (657) Google Scholar, 9Takamori S. Rhee J.S. Rosenmund C. Jahn R. Nature. 2000; 407: 189-194Crossref PubMed Scopus (705) Google Scholar). BNPI is associated with synaptic vesicles in various glutamatergic neurons (8Bellocchio E.E. Reimer R.J. Fremeau Jr., R.T. Edwards R.H. Science. 2000; 289: 957-960Crossref PubMed Scopus (657) Google Scholar, 9Takamori S. Rhee J.S. Rosenmund C. Jahn R. Nature. 2000; 407: 189-194Crossref PubMed Scopus (705) Google Scholar, 10Ni B. Wu X. Yan G.-M. Wang J. Paul S.M. J. Neurosci. 1995; 15: 5789-5799Crossref PubMed Google Scholar, 11Bellocchio E.E. Hu H. Pohorille A. Chan J. Pickel V.M. Edwards R.H. J. Neurosci. 1998; 18: 8648-8659Crossref PubMed Google Scholar). However, it is not present in all glutamatergic neurons (8Bellocchio E.E. Reimer R.J. Fremeau Jr., R.T. Edwards R.H. Science. 2000; 289: 957-960Crossref PubMed Scopus (657) Google Scholar, 9Takamori S. Rhee J.S. Rosenmund C. Jahn R. Nature. 2000; 407: 189-194Crossref PubMed Scopus (705) Google Scholar, 10Ni B. Wu X. Yan G.-M. Wang J. Paul S.M. J. Neurosci. 1995; 15: 5789-5799Crossref PubMed Google Scholar, 11Bellocchio E.E. Hu H. Pohorille A. Chan J. Pickel V.M. Edwards R.H. J. Neurosci. 1998; 18: 8648-8659Crossref PubMed Google Scholar), suggesting that another vesicular glutamate transporter(s) may function in the neurons lacking BNPI (12Otis T.S. Neuron. 2001; 29: 11-14Abstract Full Text Full Text PDF PubMed Scopus (43) Google Scholar). Differentiation-associated Na+-dependent inorganic phosphate cotransporter (DNPI), a homologue of BNPI isolated from AR42J cells differentiating into neuroendocrine cells, shows 82% amino acid identity and 92% similarity to human BNPI (13Aihara Y. Mashima H. Onda H. Hisano S. Kasuya H. Hori T. Yamada S. Tomura H. Yamada Y. Inoue I. Kojima I. Takeda J. J. Neurochem. 2000; 74: 2622-2625Crossref PubMed Scopus (237) Google Scholar). In human and rat, the DNPI gene as well as the DNPI protein was shown to be expressed in neurons in various regions, especially in the encephalon, its expression patterns being somewhat different from that of BNPI (14Hisano S. Hoshi K. Ikeda Y. Maruyama D. Kanemoto M. Ichijo H. Kojima I. Takeda J. Nogami H. Mol. Brain Res. 2000; 83: 34-43Crossref PubMed Scopus (136) Google Scholar, 15Sakata-Haga H. Kanemoto M. Maruyama D. Hoshi K. Mogi K. Narita M. Okado N. Ikeda Y. Nogami H. Fukui Y. Kojima I. Takeda J. Hisano S. Brain Res. 2001; 902: 143-155Crossref PubMed Scopus (94) Google Scholar, 16Fujiwara F. Furuta T. Kaneko T. J. Comp. Neurol. 2001; 435: 379-387Crossref PubMed Scopus (291) Google Scholar). Furthermore, DNPI was shown to be located in synaptic vesicles in the neocortex (16Fujiwara F. Furuta T. Kaneko T. J. Comp. Neurol. 2001; 435: 379-387Crossref PubMed Scopus (291) Google Scholar). One can expect that DNPI is another vesicular glutamate transporter. In the present study, we tested this hypothesis and found that DNPI shows ATP-dependent glutamate transport activity when expressed in COS7 cells. We also showed that besides its presence in neurons DNPI is also present in pinealocytes, αTC6 cells, and α and pancreatic polypeptide-secreting F cells in Langerhans islets, which contain a glutamatergic system. Pineal glands and Langerhans islets were isolated from male Wistar rats at postnatal week 6. COS7 cells and αTC6 cells, a clonal α cell line (17Hamaguchi K. Leiter E.H. Diabetes. 1990; 39: 415-425Crossref PubMed Google Scholar), were maintained in Dulbecco's modified Eagle's medium (Life Technologies, Inc.) supplemented with 10% fetal calf serum, 55 μg/ml sodium pyruvate, 4.5 g/liter glucose, 0.1 mg/liter streptomycin, 100 units/ml penicillin G, and 0.25 mg/liter Fungizone and incubated at 37 °C under 5% CO2. The dispersed cells were washed three times with the above medium, then placed in a 35-mm culture dish coated with poly-l-lysine to give 2.0 × 105cells/dish, and cultured in the above medium at 37 °C under 5% CO2. Pinealocytes were cultured as described previously (18Yamada H. Yatsushiro S. Ishio S. Hayashi M. Nishi T. Yamamoto A. Futai M. Yamaguchi A. Moriyama Y. J. Neurosci. 1998; 18: 2056-2062Crossref PubMed Google Scholar). For experimental procedures, cells were maintained for 5 days, washed with culture medium, cultured further for 1 h, and then used for experiments. Rat DNPI cDNA, as previously described (13Aihara Y. Mashima H. Onda H. Hisano S. Kasuya H. Hori T. Yamada S. Tomura H. Yamada Y. Inoue I. Kojima I. Takeda J. J. Neurochem. 2000; 74: 2622-2625Crossref PubMed Scopus (237) Google Scholar), was subcloned into the EcoRI site of expression vector pcDNA3.1 (Invitrogen, San Diego, CA). The resultant construct, DNPI-pcDNA3.1, was used to transfect COS7 cells by lipofection using Trans IT reagent (Mirus, Madison, WI). COS7 cells were grown in Dulbecco's modified Eagle's medium containing 10% fetal calf serum, penicillin, and streptomycin in a humidified incubator at 37 °C with 5% CO2. After incubation for 24 h in 35-mm dishes, DNPI-pcDNA3.1 or the pcDNA3.1 vector alone was transfected into COS7 cells by adding 2 μg of the plasmid DNA/dish. After further incubation for 48 h, the cells were rinsed with 1 ml of buffer containing 20 mm MOPS-Tris (pH 7.0), 0.3 m sucrose, 2 mm magnesium acetate, and 4 mm KCl and then used for further experiments. Total RNA extracted from isolated glands (1 μg) was transcribed into cDNA in a final volume of 20 μl of a reaction buffer containing 0.5 mm of each dNTP, 10 mm dithiothreitol, 25 pmol of random hexamers, and 200 units of Moloney murine leukemia virus reverse transcriptase (Amersham Pharmacia Biotech). After a 1-h incubation at 42 °C, the reaction was terminated by heating at 90 °C for 5 min. For PCR amplification, the 10-fold-diluted synthesized cDNA solution was added to the reaction buffer containing 1.2 mm total dNTP (300 μm of each dNTP), 6 pmol of primers, and 0.5 units of PLATINUM Pfx DNA polymerase (Life Technologies, Inc.). Thirty temperature cycles were conducted, each cycle being as follows: denaturation at 94 °C for 15 s, annealing at temperatures specific for each set of primers for 30 s, and extension at 68 °C for 1 min. The amplification products were analyzed by polyacrylamide gel electrophoresis. The sequences of the oligonucleotides used as primers were based on published sequences (13Aihara Y. Mashima H. Onda H. Hisano S. Kasuya H. Hori T. Yamada S. Tomura H. Yamada Y. Inoue I. Kojima I. Takeda J. J. Neurochem. 2000; 74: 2622-2625Crossref PubMed Scopus (237) Google Scholar): sense primer, 5′-AACACATCAACCAAGCAAGTC-3′ (bases 2304–2324); antisense primer, 5′-AGGTAGTGAATGGGAGAGCA-3′ (bases 2896–2915). For Northern blot analysis, mRNA (4.5 μg) isolated from pineal gland or other tissues was separated on a formaldehyde agarose gel (1%) and then transferred to a nylon membrane (Amersham Pharmacia Biotech). The immobilized RNA was probed with cDNA fragments of DNPI labeled with [32P]dCTP by random priming. After extensive washing, the membrane was subjected to autoradiography using BAS 1000 film (Fuji Film Co.). DNPI-expressing COS7 cells were rinsed with 1 ml of buffer comprising 20 mm MOPS-Tris (pH 7.0), 0.3 msucrose, 2 mm magnesium acetate, and 4 mm KCl. The cells were then permeabilized for 10 min at 37 °C in 0.5 ml of the same buffer containing 10 μm digitonin (19Erickson J.D. Eiden L.E. Hoffman B.J. Proc. Natl. Acad. Sci. U. S. A. 1992; 89: 10993-10997Crossref PubMed Scopus (417) Google Scholar, 20Yamada H. Otuska M. Hayashi M. Nakatsuka S. Hamaguchi K. Yamamoto A. Moriyama Y. Diabetes. 2001; 50: 1012-1020Crossref PubMed Scopus (34) Google Scholar). The medium was then replaced with fresh buffer containing Tris-ATP at 2 mm in the absence of digitonin. In some experiments, bafilomycin A1 or other chemicals were also included in the medium at the specified concentrations. Then glutamate uptake was immediately started by the addition of radioactive l-glutamate (2.5 μCi, 0.1 mm) at 37 °C as described previously (20Yamada H. Otuska M. Hayashi M. Nakatsuka S. Hamaguchi K. Yamamoto A. Moriyama Y. Diabetes. 2001; 50: 1012-1020Crossref PubMed Scopus (34) Google Scholar). After a 10-min incubation, uptake was terminated by washing the cells twice with 1 ml of ice-cold 20 mm MOPS-Tris (pH 7.0) containing 0.3 m sucrose. Then the cells were lysed with 1 ml of 1% SDS, and the radioactivity and protein concentration were measured. In some experiments, radioactive d-aspartate (2.5 μCi, 0.1 mm) was used for the substrate. Site-specific polyclonal antibodies against rat DNPI were raised in rabbits using synthetic polypeptides corresponding to the C-terminal 12 residues (C)DAYSYKDRDDYS (GenBankTM accession number AAF76223). The polypeptide was conjugated with keyhole limpet hemocyanin (Calbiochem) with m-maleimidebenzoyl-N-hydrosuccinimide ester. The monoclonal antibodies against synaptophysin and vimentin (VIM3B4) were obtained from Progen. The monoclonal antibodies against glial fibrillary acidic protein and OX42 were purchased from Reo Markers and Cosmo Bio, respectively. The mouse monoclonal antibodies against EEA1 and Rab 5, for early endosomes, and GM130, for the cis Golgi apparatus, were obtained from Transduction Laboratories. Monoclonal antibodies against protein disulfide isomerase for endoplasmic reticulum were from Fuji Yakuhin Kogyo Co. Ltd. (Toyama, Japan). The monoclonal antibodies against glucagon and insulin (MAB1) were from Sigma and Cymbus Biotechnology Ltd., respectively. The rat monoclonal antibodies against somatostatin were from Chemicon. Guinea pig polyclonal antisera against rat pancreatic polypeptide were from Linco Research, Inc. Membrane fractions (particulate fractions) of rat brain, pineal gland, Langerhans islets, and cultured cells prepared as described previously (18Yamada H. Yatsushiro S. Ishio S. Hayashi M. Nishi T. Yamamoto A. Futai M. Yamaguchi A. Moriyama Y. J. Neurosci. 1998; 18: 2056-2062Crossref PubMed Google Scholar, 20Yamada H. Otuska M. Hayashi M. Nakatsuka S. Hamaguchi K. Yamamoto A. Moriyama Y. Diabetes. 2001; 50: 1012-1020Crossref PubMed Scopus (34) Google Scholar) were denatured with SDS sample buffer containing 1% SDS and 10% β-mercaptoethanol and then electrophoresed on a 12% polyacrylamide gel in the presence of SDS. Following electrotransfer at 0.3 A for 2 h, the nitrocellulose filters were blocked in a buffer consisting of 20 mmTris-Cl (pH 7.6), 5 mm EDTA, 0.1 m NaCl, and 0.5% bovine serum albumin for 4 h and then probed with 1000-fold diluted anti-DNPI antibodies in the same buffer. The filters were washed with 20 mm Tris-Cl buffer (pH 7.6) containing 5 mm EDTA, 0.1 m NaCl, and 0.1% Tween 20, treated with peroxidase-labeled anti-rabbit IgG or anti-mouse IgG at a dilution of 1:2000 for 30 min, washed further with the same buffer, and then subjected to ECL amplification according to the manufacturer's manual (Amersham Pharmacia Biotech). The previously published procedure was used (21Hayashi M. Yamamoto A. Yatsushiro S. Yamada H. Futai M. Yamaguchi A. Moriyama Y. J. Neurochem. 1998; 71: 356-365Crossref PubMed Scopus (33) Google Scholar, 22Hayashi M. Haga M. Yatsushiro S. Yamamoto A. Moriyama Y. J. Neurochem. 1999; 73: 2538-2545Crossref PubMed Scopus (21) Google Scholar). In brief, cells on poly-l-lysine-coated glass coverslips were fixed in 4% paraformaldehyde for 20 min, washed with phosphate-buffered saline, incubated with the same buffer containing 0.1% Triton X-100 for 30 min, then further incubated with 2% goat serum and 0.5% bovine serum albumin in the same buffer, and finally incubated with antibodies at the specified dilution as described in the figure legends in phosphate-buffered saline containing 0.5% bovine serum albumin for 1 h at room temperature. The samples were washed three times with phosphate-buffered saline and then incubated with the second antibodies for 1 h at room temperature. The second antibodies used were AlexaFluor 568-labeled anti-mouse IgG at 1 μg/ml, AlexaFluor 488-labeled anti-rabbit IgG at 2 μg/ml, Cy3-labeled goat anti-rat IgG at 1 μg/ml, Cy3-labeled anti-rabbit IgG at 2 μg/ml, or fluorescein isothiocyanate-labeled anti-guinea pig IgG at 2 μg/ml. These second antibodies were obtained from Amersham Pharmacia Biotech or Molecular Probes. Finally, immunoreactivity was examined under an Olympus Fluoview FV300 confocal laser microscope. DNA sequencing was performed by the chain-termination method (23Sambrook J. Fritsch E.F. Maniatis T. Molecular Cloning: A Laboratory Manual. 2nd Ed. Cold Spring Harbor Laboratory, Cold Spring Harbor, NY1989Google Scholar). Protein concentrations were determined with a Pierce Protein Assay kit with bovine serum albumin as a standard. l-[2,3-3H]Glutamate (9.25 MBq) and d-[2,3-3H]aspartate (9.25 MBq)were obtained from PerkinElmer Life Sciences. Digitonin was purchased from Wako Chemical Co. (Osaka, Japan). Other chemicals were of the highest grade commercially available. To examine whether or not DNPI is a vesicular glutamate transporter, DNPI was expressed in COS7 cells. As shown in Fig.1 A, anti-DNPI antibodies recognized a major broad protein band corresponding to an apparent molecular mass of ∼65 kDa when DNPI-pcDNA3.1, a DNPI-expressing vector, was transfected to COS7 cells. The molecular mass corresponding to the DNPI immunoreactivity is similar to that expected from its primary amino acid sequence and DNPI from the brain (Fig.1 A). Two additional protein bands with apparent molecular masses of ∼72 and ∼42 kDa were also observed. Neither untransfected control COS7 cells nor COS cells transfected with a control vector expressed any DNPI gene, as revealed on RT-PCR analysis (data not shown), or the immunoreactive polypeptide (Fig. 1 A). The DNPI immunoreactivity disappeared when the antigenic polypeptide was included during antibody treatment (Fig. 1 A). These results indicated that DNPI is expressed in COS7 cells. The expressed DNPI was distributed throughout COS7 cells (Fig.1 B). Immunohistochemical analysis indicated that DNPI is co-localized with EEA1 or Rab 5, early endosomal markers (Fig.1 C). DNPI is partially co-localized with GM130, a marker protein of the cis Golgi apparatus but not with protein disulfide isomerase, a marker protein of endoplasmic reticulum (Fig.1 C). These results suggest that DNPI is mainly associated with early endosomes in the cells. We examined whether or not DNPI shows vesicular glutamate transport activity. As shown in Fig. 1 D, digitonin-permeabilized DNPI-expressing cells took up radiolabeled l-glutamate depending on ATP. Neither untransfected control cells nor cells transfected with a control vector showed ATP-dependent glutamate uptake activity. The omission of Mg2+ reduced the ATP-dependent l-glutamate uptake to the control level. Bafilomycin A1, a specific inhibitor of vacuolar H+-ATPase (24Bowman E.J. Siebers A. Altendorf K. Proc. Natl. Acad. Sci. U. S. A. 1988; 85: 7972-7976Crossref PubMed Scopus (1582) Google Scholar), at 1 μm inhibited the ATP-dependent l-glutamate uptake. SF6847, a proton conductor that dissipates an electrochemical proton gradient, also inhibited the ATP-dependent l-glutamate uptake. In contrast, vanadate (1 mm), an inhibitor of P-type ion-transporting ATPases, did not affect the ATP-dependent glutamate uptake. These results indicated that the glutamate uptake is driven by an electrochemical gradient of protons established by vacuolar H+-ATPase. The addition of either l-aspartate or d-aspartate at 1.0 mm during the assay had a little effect on the ATP-dependent glutamate uptake, indicating that the glutamate transporter does not recognize l-aspartate ord-aspartate as a substrate, one of the characteristics of vesicular glutamate transporters (25Naito S. Ueda T. J. Neurochem. 1985; 44: 99-109Crossref PubMed Scopus (375) Google Scholar, 26Maycox P.R. Deckwerth T. Hell J.W. Jahn R. J. Biol. Chem. 1988; 263: 15423-15428Abstract Full Text PDF PubMed Google Scholar, 27Moriyama Y. Yamamoto A. J. Biol. Chem. 1995; 270: 22314-22320Abstract Full Text Full Text PDF PubMed Scopus (85) Google Scholar). The inability of DNPI to transport d-aspartate was also confirmed by the direct uptake assay (Fig. 1 D). Together these results indicate that DNPI is responsible for the vesicular storage ofl-glutamate. Besides the central nervous system, peripheral endocrine tissues possess glutamatergic systems (3Moriyama Y. Yamamoto A. Yamada H. Tashiro Y. Futa M. Biol. Chem. 1996; 377: 155-165PubMed Google Scholar, 4Moriyama Y. Hayashi M. Yamada H. Yatsushiro S. Ishio S. Yamamoto A. J. Exp. Biol. 2000; 203: 117-125PubMed Google Scholar). Mammalian pinealocytes accumulatel-glutamate in SLMVs, counterparts of synaptic vesicles in endocrine cells, and secrete it to the extracellular space through exocytosis (28Yamada H. Yamamoto A. Yodozawa S. Nozaki S. Takahashi M. Michibata H. Morita M. Furuichi T. Mikoshiba K. Moriyama Y. J. Pineal Res. 1996; 21: 175-191Crossref PubMed Scopus (53) Google Scholar, 29Yatsushiro S. Yamada H. Kozaki S. Kumon H. Michibata H. Yamamoto A. Moriyama Y. J. Neurochem. 1997; 69: 340-347Crossref PubMed Scopus (56) Google Scholar). Vesicular glutamate transporter is responsible for the storage of l-glutamate in pineal SLMVs (27Moriyama Y. Yamamoto A. J. Biol. Chem. 1995; 270: 22314-22320Abstract Full Text Full Text PDF PubMed Scopus (85) Google Scholar, 30Moriyama Y. Yamamoto A. FEBS Lett. 1995; 367: 233-236Crossref PubMed Scopus (61) Google Scholar). To determine whether or not DNPI is expressed in pinealocytes, expression of the DNPI gene in pineal gland was examined by RT-PCR using specific DNA probes. As shown in Fig.2 A, amplified products of expected size for DNPI were obtained when total RNAs isolated from pineal glands and cultured pineal cells as well as brain were used. The nucleotide and deduced amino acid sequences of the amplified products exactly matched that of the DNPI gene. Northern blot analysis with the amplified RT-PCR products further demonstrated the expression of mRNA for DNPI in pineal glands: two major bands (∼3.2 and 4.1 kilobases) for pineal glands and brain mRNA were detected (Fig. 2 B). Western blot analysis indicated that the anti-DNPI antibodies recognized a single polypeptide of ∼65 kDa in pineal glands, cultured pinealocytes, and brain membranes (Fig.2 C). The DNPI immunoreactivity was blocked when the nitrocellulose sheet was treated with an antigenic peptide during the immunodecoration (Fig. 2 C). Overall it is concluded that DNPI is expressed in pineal glands and cultured pinealocytes. Immunohistochemistry with frozen-sectioned pineal gland revealed the localization of DNPI at the cellular level. We used the following cell markers to classify DNPI-positive cells: synaptophysin for pinealocytes (30Moriyama Y. Yamamoto A. FEBS Lett. 1995; 367: 233-236Crossref PubMed Scopus (61) Google Scholar, 31Redecker P. Bargsten G. J. Neurosci. Res. 1993; 34: 79-96Crossref PubMed Scopus (65) Google Scholar), glial fibrillary acidic protein for astrocytes (32Papasozomenos S.C. J. Neuropathol. Exp. Neurol. 1983; 42: 391-408Crossref PubMed Scopus (44) Google Scholar), OX42 for microglia (33Pedersen E.B. Fox L.M. Castro A.J. McNulty J.A. Cell Tissue Res. 1993; 272: 257-265Crossref PubMed Scopus (51) Google Scholar), and vimentin for interstitial cells (34Schachner M. Huang S.K. Ziegelmuller P. Bizzini B. Taugner R. Cell Tissue Res. 1984; 237: 245-252Crossref PubMed Scopus (57) Google Scholar). The antibodies against these marker proteins immunostained the corresponding populations of pineal cells with a similar morphology as reported previously (33Pedersen E.B. Fox L.M. Castro A.J. McNulty J.A. Cell Tissue Res. 1993; 272: 257-265Crossref PubMed Scopus (51) Google Scholar, 35Yamada H. Yatsushiro S. Yamamoto A. Nishi T. Futai M. Yamaguchi A. Moriyama Y. J. Neurochem. 1997; 69: 1491-1498Crossref PubMed Scopus (39) Google Scholar) (Fig. 2 D). The DNPI-positive cells coincided with synaptophysin but not with any of the above-mentioned cell markers, indicating that pinealocytes contain DNPI (Fig. 2 D). Essentially the same results were obtained for cultured pineal cells (data not shown). DNPI and synaptophysin are enriched in the process terminal regions, the site for glutamate exocytosis (3Moriyama Y. Yamamoto A. Yamada H. Tashiro Y. Futa M. Biol. Chem. 1996; 377: 155-165PubMed Google Scholar, 4Moriyama Y. Hayashi M. Yamada H. Yatsushiro S. Ishio S. Yamamoto A. J. Exp. Biol. 2000; 203: 117-125PubMed Google Scholar) (Fig. 2 E). These results strongly suggested that DNPI is associated with SLMVs in pinealocytes. Langerhans islets express various types of ionotropic glutamate receptors and reuptake systems (36Inagaki N. Kuromi H. Gonoi T. Okamoto Y. Ishida H. Seino Y. Kaneko T. Iwanaga T. Seino S. FASEB J. 1995; 9: 686-691Crossref PubMed Scopus (172) Google Scholar, 37Weaver C.D. Yao T.L. Powers A.C. Verdoon T.A. J. Biol. Chem. 1996; 271: 12977-12984Abstract Full Text Full Text PDF PubMed Scopus (103) Google Scholar, 38Weaver C.D. Gundersen V. Verdoorn T.A. J. Biol. Chem. 1998; 273: 1647-1653Abstract Full Text Full Text PDF PubMed Scopus (40) Google Scholar). Clonal pancreatic αTC6 cells store and secretel-glutamate through exocytosis, the mechanism being similar to those in neurons and pinealocytes (20Yamada H. Otuska M. Hayashi M. Nakatsuka S. Hamaguchi K. Yamamoto A. Moriyama Y. Diabetes. 2001; 50: 1012-1020Crossref PubMed Scopus (34) Google Scholar). Thus, it is possible that Langerhans islets are another example of an endocrine glutamatergic system and that DNPI is responsible for the storage ofl-glutamate in the islets. To examine this possibility, the expression of DNPI in αTC6 cells and islets was measured. RT-PCR analysis indicated the presence of DNPI mRNA in αTC6 cells (Fig.3 A). Western blotting and immunohistochemistry indicated the presence of DNPI in αTC6 cells (Fig. 3, B and C). Langerhans islets are composed of four major types of endocrine cells,i.e. insulin-secreting β cells, glucagon-secreting α cells, pancreatic polypeptide-secreting F cells, and somatostatin-secreting δ cells. Western blotting clearly indicated the presence of DNPI in the islets (Fig. 3 B). DNPI was co-localized with glucagon but not with insulin or somatostatin in horizontal sections of the islets, indicating the presence of DNPI in α cells but not in β or δ cells (Fig. 3 C). DNPI is also co-localized with pancreatic polypeptides. These results suggested that DNPI is mainly present in α cells and partially in pancreatic polypeptide-secreting F cells (Fig. 3 C). Vesicular glutamate transporter is responsible for the glutamatergic characteristics of neurons and was originally identified in synapsin I-associated synaptic vesicles (25Naito S. Ueda T. J. Neurochem. 1985; 44: 99-109Crossref PubMed Scopus (375) Google Scholar, 39Naito S. Ueda T. J. Biol. Chem. 1983; 258: 696-699Abstract Full Text PDF PubMed Google Scholar). In the earlier stage of studies, vesicular glutamate transporter was defined as the ATP-dependent proton conductor-sensitive glutamate transport activity in synaptic vesicles, but little was known about the protein nature of the transporter at the molecular level (25Naito S. Ueda T. J. Neurochem. 1985; 44: 99-109Crossref PubMed Scopus (375) Google Scholar, 26Maycox P.R. Deckwerth T. Hell J.W. Jahn R. J. Biol. Chem. 1988; 263: 15423-15428Abstract Full Text PDF PubMed Google Scholar, 27Moriyama Y. Yamamoto A. J. Biol. Chem. 1995; 270: 22314-22320Abstract Full Text Full Text PDF PubMed Scopus (85) Google Scholar, 39Naito S. Ueda T. J. Biol. Chem. 1983; 258: 696-699Abstract Full Text PDF PubMed Google Scholar). In the last year, two groups have independently reported that BNPI is vesicular glutamate transporter itself and that BNPI is a potential tool for substantial studies on vesicular glutamate transporter. DNPI is a potential candidate for another vesicular glutamate transporter since DNPI is distributed throughout the brain, being especially abundant in the nerve endings of glutamatergic neurons where BNPI is scarce (15Sakata-Haga H. Kanemoto M. Maruyama D. Hoshi K. Mogi K. Narita M. Okado N. Ikeda Y. Nogami H. Fukui Y. Kojima I. Takeda J. Hisano S. Brain Res. 2001; 902: 143-155Crossref PubMed Scopus (94) Google Scholar, 16Fujiwara F. Furuta T. Kaneko T. J. Comp. Neurol. 2001; 435: 379-387Crossref PubMed Scopus (291) Google Scholar). Here we showed that DNPI actually functions as a vesicular glutamate transporter when expressed in COS7 cells. DNPI expressed in COS7 cells seems to be mainly localized in endosomes. Since endosomes contain vacuolar H+-ATPase (40Stevens T.H. Forgac M. Annu. Rev. Cell Dev. Biol. 1997; 13: 779-808Crossref PubMed Scopus (516) Google Scholar, 41Nerlson N. Harvey W.R. Physiol. Rev. 1999; 79: 361-385Crossref PubMed Scopus (363) Google Scholar), the active transport of glutamate into the organelles should be expected upon the addition of ATP in digitonin-permeabilized cells. In fact, digitonin-permeabilized cells took up l-glutamate depending on MgATP, and the properties of the uptake are consistent with those of vesicular glutamate transporter (25Naito S. Ueda T. J. Neurochem. 1985; 44: 99-109Crossref PubMed Scopus (375) Google Scholar, 26Maycox P.R. Deckwerth T. Hell J.W. Jahn R. J. Biol. Chem. 1988; 263: 15423-15428Abstract Full Text PDF PubMed Google Scholar, 27Moriyama Y. Yamamoto A. J. Biol. Chem. 1995; 270: 22314-22320Abstract Full Text Full Text PDF PubMed Scopus (85) Google Scholar, 39Naito S. Ueda T. J. Biol. Chem. 1983; 258: 696-699Abstract Full Text PDF PubMed Google Scholar), indicating that DNPI expressed functions as a vesicular glutamate transporter. The fact that DNPI exhibits vesicular glutamate transport activity is not surprising since the amino acid identity of the core portions of DNPI and BNPI excluding their hydrophilic N- and C-terminal regions is over 90% with 12 putative transmembrane helices (7Ni B. Rosteck Jr., P.R. Nadi N.S. Paul S.M. Proc. Natl. Acad. Sci. U. S. A. 1994; 91: 5607-5611Crossref PubMed Scopus (274) Google Scholar, 13Aihara Y. Mashima H. Onda H. Hisano S. Kasuya H. Hori T. Yamada S. Tomura H. Yamada Y. Inoue I. Kojima I. Takeda J. J. Neurochem. 2000; 74: 2622-2625Crossref PubMed Scopus (237) Google Scholar). In the original studies on the expression and functions of BNPI and DNPI, both proteins were found to facilitate the transport of inorganic phosphate depending on extracellular Na+ (7Ni B. Rosteck Jr., P.R. Nadi N.S. Paul S.M. Proc. Natl. Acad. Sci. U. S. A. 1994; 91: 5607-5611Crossref PubMed Scopus (274) Google Scholar, 13Aihara Y. Mashima H. Onda H. Hisano S. Kasuya H. Hori T. Yamada S. Tomura H. Yamada Y. Inoue I. Kojima I. Takeda J. J. Neurochem. 2000; 74: 2622-2625Crossref PubMed Scopus (237) Google Scholar). On the other hand, vesicular glutamate transporters use a proton as a coupling ion and only recognize l-glutamate and a few cyclic glutamate analogues as substrates (25Naito S. Ueda T. J. Neurochem. 1985; 44: 99-109Crossref PubMed Scopus (375) Google Scholar, 26Maycox P.R. Deckwerth T. Hell J.W. Jahn R. J. Biol. Chem. 1988; 263: 15423-15428Abstract Full Text PDF PubMed Google Scholar, 27Moriyama Y. Yamamoto A. J. Biol. Chem. 1995; 270: 22314-22320Abstract Full Text Full Text PDF PubMed Scopus (85) Google Scholar, 39Naito S. Ueda T. J. Biol. Chem. 1983; 258: 696-699Abstract Full Text PDF PubMed Google Scholar). Thus, DNPI and BNPI are versatile in their coupling ions and substrate specificity in nature. Further studies will be necessary to elucidate the molecular mechanism underlying the versatility and to assign the domains responsible for the Na+-dependent inorganic phosphate transport and proton-coupled glutamate transport. A significant finding in this study is that DNPI is expressed in glutamatergic endocrine cells. Recent studies have revealed that some endocrine cells secrete l-glutamate through exocytosis, and the released glutamate may function as a paracrine or autocrine chemical transmitter by way of a glutamate receptor expressed on the same or neighboring cells (3Moriyama Y. Yamamoto A. Yamada H. Tashiro Y. Futa M. Biol. Chem. 1996; 377: 155-165PubMed Google Scholar, 4Moriyama Y. Hayashi M. Yamada H. Yatsushiro S. Ishio S. Yamamoto A. J. Exp. Biol. 2000; 203: 117-125PubMed Google Scholar). Vesicular glutamate transporters play a key role in glutamate signal output through the storage ofl-glutamate in endocrine cells. Consistent with the presence of glutamatergic systems, DNPI is present in pinealocytes and is co-localized with SLMVs. Thus, DNPI may function to storel-glutamate in SLMVs and secrete it through exocytosis, which is one of the components of the negative regulatory mechanism for melatonin synthesis. Not all pinealocytes processes are positive for DNPI (Fig. 2 E, arrows and arrowheads), indicating the functional heterogeneity of SLMVs in pinealocytes as suggested by Redecker (42Redecker P. Int. Rev. Cytol. 1999; 191: 201-255Crossref PubMed Google Scholar). It should be emphasized that DNPI is present in αTC6 cells and α cells in Langerhans islets. DNPI is also present in pancreatic polypeptide-secreting F cells, suggesting that pancreatic polypeptide-secreting F cells are capable of storing and secretingl-glutamate. Therefore, α cells and possibly pancreatic peptide-secreting F cells are the sites for the glutamate release in the islets, which was first proposed by Weaver et al. (38Weaver C.D. Gundersen V. Verdoorn T.A. J. Biol. Chem. 1998; 273: 1647-1653Abstract Full Text Full Text PDF PubMed Scopus (40) Google Scholar). Thus, Langerhans islets may equip their own input, output, and termination systems for glutamate signals. Although the physiological role(s) of the glutamatergic system in the islets is not fully understood at present, the glutamate may regulate the secretion of insulin and glucagon by way of its binding to the receptors in α and β cells (43Bertrand G. Gross R. Puech R. Loubatieres-Mariani M.M. Bockaert J. Br. J. Pharmacol. 1992; 106: 354-359Crossref PubMed Scopus (96) Google Scholar, 44Bertrand G. Gross R. Puech R. Loubatieres-Mariani M.M. Bockaert J. Eur. J. Pharmacol. 1993; 237: 45-50Crossref PubMed Scopus (85) Google Scholar). A role of l-glutamate as an intracellular signaling molecule in β cells, which enhances the second phase of insulin secretion, has also been postulated (45Maechler P. Wollheim C.B. Nature. 1999; 402: 685-689Crossref PubMed Scopus (433) Google Scholar). In conclusion, DNPI is an indicator for glutamatergic systems in peripheral tissues as well as neurons and is a very useful probe for studies on peripheral glutamatergic systems. We are extensively studying the localization of DNPI in various organs, which will reveal the site where l-glutamate acts as an intercellular signaling molecule in peripheral organs. Just before our submission, Bai et al.(46Bai L. Xu H. Collins J.F. Ghishan F.K. J. Biol. Chem. 2001; 276: 36764-36769Abstract Full Text Full Text PDF PubMed Scopus (173) Google Scholar) cloned mouse cDNA similar to DNPI. When this cDNA was expressed in PC12 cells, the vesicular glutamate transport activity appeared." @default.
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• W2039813168 title "Differentiation-associated Na+-dependent Inorganic Phosphate Cotransporter (DNPI) Is a Vesicular Glutamate Transporter in Endocrine Glutamatergic Systems" @default.
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