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1.
J Neurosci ; 21(19): RC168, 2001 Oct 01.
Article in English | MEDLINE | ID: mdl-11567079

ABSTRACT

Orexins (also called hypocretins) are peptide neurotransmitters expressed in neurons of the lateral hypothalamic area (LHA). Mice lacking the orexin peptides develop narcolepsy-like symptoms, whereas mice with a selective loss of the orexin neurons develop hypophagia and severe obesity in addition to the narcolepsy phenotype. These different phenotypes suggest that orexin neurons may contain neurotransmitters besides orexin that regulate feeding and energy balance. Dynorphin neurons are common in the LHA, and dynorphin has been shown to influence feeding; hence, we studied whether dynorphin and orexin are colocalized. In rats, double-label in situ hybridization revealed that nearly all (94%) neurons expressing prepro-orexin mRNA also expressed prodynorphin mRNA. The converse was also true: 96% of neurons in the LHA containing prodynorphin mRNA also expressed prepro-orexin mRNA. Double-label immunohistochemistry confirmed that orexin-A and dynorphin-A peptides were highly colocalized in the LHA. Wild-type mice and orexin knock-out mice showed abundant prodynorphin mRNA-expressing neurons in the LHA, but orexin/ataxin-3 mice with a selective loss of the orexin neurons completely lacked prodynorphin mRNA in this area, further confirming that within the LHA, dynorphin expression is restricted to the orexin neurons. These findings suggest that dynorphin-A may play an important role in the function of the orexin neurons.


Subject(s)
Carrier Proteins/metabolism , Dynorphins/metabolism , Intracellular Signaling Peptides and Proteins , Neurons/metabolism , Neuropeptides/metabolism , Protein Precursors/metabolism , Animals , Ataxin-3 , Carrier Proteins/genetics , Dynorphins/genetics , Fornix, Brain/cytology , Fornix, Brain/metabolism , Hypothalamus/cytology , Hypothalamus/metabolism , Immunohistochemistry , In Situ Hybridization , Mice , Mice, Inbred C57BL , Mice, Inbred DBA , Mice, Knockout , Mice, Transgenic , Nerve Tissue Proteins/genetics , Neuropeptides/deficiency , Neuropeptides/genetics , Nuclear Proteins , Orexins , Protein Precursors/genetics , RNA, Messenger/metabolism , Rats , Rats, Sprague-Dawley , Repressor Proteins , Transcription Factors
2.
Neuron ; 30(2): 345-54, 2001 May.
Article in English | MEDLINE | ID: mdl-11394998

ABSTRACT

Orexins (hypocretins) are a pair of neuropeptides implicated in energy homeostasis and arousal. Recent reports suggest that loss of orexin-containing neurons occurs in human patients with narcolepsy. We generated transgenic mice in which orexin-containing neurons are ablated by orexinergic-specific expression of a truncated Machado-Joseph disease gene product (ataxin-3) with an expanded polyglutamine stretch. These mice showed a phenotype strikingly similar to human narcolepsy, including behavioral arrests, premature entry into rapid eye movement (REM) sleep, poorly consolidated sleep patterns, and a late-onset obesity, despite eating less than nontransgenic littermates. These results provide evidence that orexin-containing neurons play important roles in regulating vigilance states and energy homeostasis. Orexin/ataxin-3 mice provide a valuable model for studying the pathophysiology and treatment of narcolepsy.


Subject(s)
Carrier Proteins/metabolism , Feeding and Eating Disorders/genetics , Hypothalamus/physiopathology , Intracellular Signaling Peptides and Proteins , Narcolepsy/genetics , Nerve Tissue Proteins/genetics , Neurons/physiology , Neuropeptides/metabolism , Neurotransmitter Agents/metabolism , Obesity/genetics , Sleep Stages/genetics , Animals , Ataxin-3 , Feeding and Eating Disorders/physiopathology , Female , Humans , Hypothalamus/pathology , Machado-Joseph Disease/genetics , Male , Mice , Mice, Inbred C57BL , Mice, Inbred DBA , Mice, Transgenic , Narcolepsy/physiopathology , Nerve Tissue Proteins/chemistry , Nerve Tissue Proteins/metabolism , Neurons/pathology , Nuclear Proteins , Obesity/physiopathology , Orexins , Peptides/genetics , Repressor Proteins , Sequence Deletion , Sleep Stages/physiology , Sleep, REM/genetics , Transcription Factors
3.
J Comp Neurol ; 428(1): 62-78, 2000 Dec 04.
Article in English | MEDLINE | ID: mdl-11058225

ABSTRACT

We applied high-resolution laser-scanning microscopy, electron microscopy, and non-radioactive in situ hybridization histochemistry to determine the cellular and intracellular localization of lipocalin-type prostaglandin D synthase, the major brain-derived protein component of cerebrospinal fluid, and its mRNA in leptomeninges, choroid plexus, and parenchyma of the adult rat brain. Both immunoreactivity and mRNA for prostaglandin D synthase were located in arachnoid barrier cells, arachnoid trabecular cells, and arachnoid pia mater cells. Furthermore, meningeal macrophages and perivascular microglial cells, identified by use of ED2 antibody, were immunopositive for prostaglandin D synthase. In the arachnoid trabecular cells, the immunoreactivity for prostaglandin D synthase was located in the nuclear envelope, Golgi apparatus, and secretory vesicles, indicating the active production and secretion of prostaglandin D synthase. In the meningeal macrophages, prostaglandin D synthase was not found around the nucleus but in lysosomes in the cytoplasm, pointing to an uptake of the protein from the cerebrospinal fluid. Furthermore, the existence of meningeal cyclooxygenase (COX) -1 and COX-2 was investigated by Western blot, Northern blot, and reverse transcriptase-polymerase chain reaction (RT-PCR), and the colocalization of COX-2 and prostaglandin D synthase was demonstrated in virtually all cells of the leptomeninges, choroid plexus epithelial cells, and perivascular microglial cells, suggesting that these cells synthesize prostaglandin D(2) actively. Alternatively, oligodendrocytes showed prostaglandin D synthase immunoreactivity without detectable COX-2. The localization of lipocalin-type prostaglandin D synthase in meningeal cells and its colocalization with COX-2 provide evidence for its function as a prostaglandin D(2)-producing enzyme.


Subject(s)
Central Nervous System/enzymology , Intramolecular Oxidoreductases/metabolism , Meninges/enzymology , Rats, Sprague-Dawley/metabolism , Animals , Arachnoid/metabolism , Arachnoid/ultrastructure , Brain/metabolism , Brain/ultrastructure , Central Nervous System/ultrastructure , Choroid Plexus/metabolism , Choroid Plexus/ultrastructure , Cyclooxygenase 1 , Cyclooxygenase 2 , Intramolecular Oxidoreductases/genetics , Isoenzymes/genetics , Isoenzymes/metabolism , Lipocalins , Male , Membrane Proteins , Meninges/ultrastructure , Pia Mater/metabolism , Pia Mater/ultrastructure , Prostaglandin-Endoperoxide Synthases/genetics , Prostaglandin-Endoperoxide Synthases/metabolism , RNA, Messenger/metabolism , Rats , Rats, Sprague-Dawley/anatomy & histology
4.
Neurochem Res ; 25(5): 733-8, 2000 May.
Article in English | MEDLINE | ID: mdl-10905636

ABSTRACT

Cytosolic prostaglandin (PG) E synthase was purified from human brain cortex. The N-terminal amino acid sequence, PMTLGYXNIRGL, was identical to that of the human mu-class glutathione transferase (GST) M2 subunit. Complementary DNAs for human GSTM2, GSTM3, and GSTM4 subunits were cloned, and recombinant proteins were expressed as homodimers in Escherichia coli. The recombinant GSTM2-2 and 3-3 catalyzed the conversion of PGH2 to PGE2 at the rates of 282 and 923 nmol/min/mg of protein, respectively, at the optimal pH of 8, whereas GSTM4-4 was inactive; although all three enzymes showed GST activity. The PGE synthase activity depended on thiols, such as glutathione, dithiothreitol, 2-mercaptoethanol, or L-cysteine. Michaelis-Menten constants and turnover numbers for PGH2 were 141 microM and 10.8 min(-1) for GSTM2-2 and 1.5 mM and 130 min(-1) for GSTM3-3, respectively. GSTM2-2 and 3-3 may play crucial roles in temperature regulation, nociception, and sleep-wake regulation by producing PGE2 in the brain.


Subject(s)
Cerebral Cortex/enzymology , Glutathione Transferase/metabolism , Intramolecular Oxidoreductases/metabolism , Amino Acid Sequence , Cloning, Molecular , Cytosol/enzymology , Glutathione Transferase/chemistry , Glutathione Transferase/genetics , Humans , Intramolecular Oxidoreductases/chemistry , Intramolecular Oxidoreductases/genetics , Isoenzymes/chemistry , Isoenzymes/genetics , Isoenzymes/metabolism , Kinetics , Peptide Fragments/chemistry , Prostaglandin-E Synthases , Protein Subunits , Recombinant Proteins/chemistry , Recombinant Proteins/metabolism , Substrate Specificity , Sulfhydryl Compounds/metabolism
5.
Brain Res Brain Res Protoc ; 5(3): 248-56, 2000 Jul.
Article in English | MEDLINE | ID: mdl-10906490

ABSTRACT

Studies on drug entry into the brain and permeation of the blood-brain barrier start to gain more and more importance in neuropharmaceutical research in order to develop new drugs for the therapy of central nervous system diseases. Procedures that provide quick access to permeation properties of those drugs with high throughput are difficult to achieve with animal models. Although various useful cell culture models approaching this issue have been described, results are often not comparable among each other unless determined with an equal experimental setup. Reproducibility of cell culture methods as well as corresponding findings gathered with these tools are often impeded due to the lack of details in experimental manuals. Here we present a precise manual for preparation and maintenance of porcine brain microvessel endothelial cells, serving as a culture model of the blood-brain barrier. Furthermore experimental details for blood-brain barrier transport investigations are presented. Validation of this model was carried out by determination of bioelectric properties and permeation experiments using various marker molecules reflecting paracellular and transcellular blood-brain barrier penetration. Results obtained with our model are closely resembling the in vivo-situation although astrocytes are not included. This simplification of the system is one of the major advantages towards robot derived cell cultures necessary for high throughput screening.


Subject(s)
Blood-Brain Barrier/physiology , Brain/blood supply , Cell Culture Techniques/methods , Endothelium, Vascular/cytology , Retinoids/pharmacokinetics , Animals , Blood Proteins/pharmacology , Blood-Brain Barrier/drug effects , Capillaries/cytology , Collagen/isolation & purification , Collagen/pharmacology , Culture Media, Serum-Free/pharmacology , Female , Male , Rats , Rats, Wistar , Swine
6.
Biochemistry ; 38(25): 8006-13, 1999 Jun 22.
Article in English | MEDLINE | ID: mdl-10387044

ABSTRACT

Lipocalin-type prostaglandin D synthase is a major protein of the cerebrospinal fluid and was originally known as beta-trace. We investigated the binding ability of prostaglandin D synthase toward bile pigments, thyroid hormones, steroid hormones, and fatty acids in this present study. We found that the recombinant enzyme binds bile pigments and thyroid hormones, resulting in quenching of the intrinsic tryptophan fluorescence, the appearance of induced circular dichroism of the lipophilic ligands, and a red shift of the absorption spectra of bilirubin and biliverdin. The binding of prostaglandin D synthase to lipophilic ligands was also demonstrated by the resonant mirror technique and surface plasmon resonance detection. The dissociation constants were calculated to be 33 nM, 37 nM, 660 nM, 820 nM, and 2.08 microM for biliverdin, bilirubin, L-thyroxine, 3,3',5'-triiodo-L-thyronine, and 3,3', 5-triiodo-L-thyronine, respectively. Biliverdin and bilirubin underwent a shift in their absorption peaks from 375 to 380 nm and from 439 to 446 nm, respectively, after binding to prostaglandin D synthase. Bilirubin bound to the enzyme showed a bisignate CD spectrum with a (-) Cotton effect at 422 nm and a (+) Cotton effect at 472 nm, indicating a right-handed chirality. The ligands also inhibited prostaglandin D synthase activity noncompetitively in a concentration-dependent manner, with IC50 values between 3.9 and 10. 9 microM. Epididymal retinoic acid-binding protein and beta-lactoglobulin, two other lipocalin proteins that bind retinoids such as prostaglandin D synthase, did not show any significant interaction with bile pigments or thyroid hormones. These results show that prostaglandin D synthase binds small lipophilic ligands with a specificity distinct from that of other lipocalins.


Subject(s)
Bilirubin/chemistry , Biliverdine/chemistry , Carrier Proteins/chemistry , Intramolecular Oxidoreductases/chemistry , Neoplasm Proteins , Nerve Tissue Proteins , Thyroid Hormones/chemistry , Animals , Beta-Globulins/chemistry , Beta-Globulins/metabolism , Bilirubin/metabolism , Biliverdine/metabolism , Carrier Proteins/metabolism , Enzyme Inhibitors/chemistry , Fatty Acid-Binding Protein 7 , Fatty Acid-Binding Proteins , Intramolecular Oxidoreductases/antagonists & inhibitors , Intramolecular Oxidoreductases/metabolism , Lactoglobulins/chemistry , Ligands , Lipocalins , Models, Molecular , Myelin P2 Protein/chemistry , Myelin P2 Protein/metabolism , Rats , Receptors, Retinoic Acid/chemistry , Receptors, Retinoic Acid/metabolism , Spectrometry, Fluorescence , Thyroid Hormones/metabolism
7.
Brain Res ; 818(1): 65-71, 1999 Feb 06.
Article in English | MEDLINE | ID: mdl-9914438

ABSTRACT

Primary cultures of porcine brain capillary endothelial cells grown on collagen coated polycarbonate membranes were used to build up an in vitro-model for the blood-brain barrier. Improved cultivation techniques allowed cell-storage and experiments under serum-free conditions. We employed this model to perform permeability studies in vitro with the radioactively labelled marker substances sucrose, retinoic acid, retinol, haloperidol, caffeine, and mannitol. Permeability values obtained with this blood-brain barrier model (1. 0x10-6 cm/s for sucrose, 6.2x10-6 cm/s for retinoic acid, 4.8x10-6 cm/s for retinol, 49.5x10-6 cm/s for haloperidol, 62.4x10-6 cm/s for caffeine, and 1.8x10-6 cm/s for mannitol) show a good correlation to data which are already known from in vivo-experiments. As judged by the sucrose permeability our blood-brain barrier model is less permeable than numerous other models published so far. Therefore it represents a powerful tool for in vitro-prediction of blood-brain barrier permeability of drugs and offers the possibility to scan a large quantity of drugs for their potential to enter the brain.


Subject(s)
Blood-Brain Barrier/physiology , Caffeine/pharmacokinetics , Haloperidol/pharmacokinetics , Mannitol/pharmacokinetics , Retinoids/pharmacokinetics , Sucrose/pharmacokinetics , Animals , Cells, Cultured , Colchicine/pharmacology , Culture Media, Serum-Free , Endothelium, Vascular/cytology , Endothelium, Vascular/metabolism , Swine
9.
J Neurochem ; 71(3): 937-45, 1998 Sep.
Article in English | MEDLINE | ID: mdl-9721719

ABSTRACT

Prostaglandin (PG) D2 is one of the major prostanoids in the mammalian brain and eye tissues. Its function is mediated by the prostanoid DP receptor, which is specific for PGD2 among the various prostanoids. In this study, we cloned the full-length cDNA for the rat DP receptor and used it for detection of DP receptor mRNA in various rat tissues. Northern blotting and RT-PCR analyses revealed that this DP receptor was expressed most intensely in the eye tissues, moderately in the leptomeninges and oviduct, and weakly in the epididymis. The tissue distribution profile of the mRNA for the rat DP receptor is overlapped with those of hematopoietic and lipocalin-type PGD synthases. Among rat eye tissues, the expression was the highest in the iris. In situ hybridization and in situ RT-PCR revealed DP receptor mRNA to be localized in the epithelium of the iris and ciliary body and in photoreceptor cells of the retina, suggesting the involvement of the receptor in the physiological regulation of intraocular pressure and the vision process. In the brain, DP receptor mRNA was dominantly expressed in the leptomeninges and was not detected in the brain parenchyma including the ventral rostral forebrain, the surface area of which is reportedly involved in sleep induction by PGD2.


Subject(s)
Arachnoid/metabolism , Eye/metabolism , Pia Mater/metabolism , RNA, Messenger/metabolism , Receptors, Immunologic , Receptors, Prostaglandin/genetics , Amino Acid Sequence , Animals , Ciliary Body/metabolism , Epithelium/metabolism , Female , Genes, Dominant/genetics , Iris/metabolism , Male , Molecular Sequence Data , Photoreceptor Cells/metabolism , Rats , Rats, Sprague-Dawley , Sequence Homology, Amino Acid
10.
Invest Ophthalmol Vis Sci ; 39(1): 198-203, 1998 Jan.
Article in English | MEDLINE | ID: mdl-9430563

ABSTRACT

PURPOSE: Prostaglandin (PG) D synthase is present in neural tissues and cerebrospinal fluid (beta-trace). This enzyme belongs to the lipocalin family which consists of transporter proteins for lipophilic substances in the extracellular space. PGD synthase is found in retinal pigment epithelium, from where it is secreted into the interphotoreceptor matrix. The authors have undertaken the localization of this unique enzyme within the tissues and spaces of the anterior segment of the eye. METHODS: Iris, ciliary body, lens, and aqueous and vitreous humors were collected from adult rats and mice. PGD synthase activity was determined, and the protein was quantified by Western blot analysis and localized immunohistochemically. Finally, in situ hybridization was performed to localize PGD synthase mRNA. RESULTS: PGD synthase was most abundant in the aqueous and vitreous humors. It was less abundant in tissue cytosolic fractions; these fractions had almost 10-fold as much as their corresponding membrane-bound fractions. Lens tissue had the lowest amount observed. PGD synthase was localized to the epithelial cells of the iris and the ciliary body and to the adjacent extracellular chambers, but PGD synthase mRNA was found only within the epithelial cells. Several glycosylated forms of PGD synthase were also detected. CONCLUSIONS: PGD synthase was synthesized within the epithelial cells of the iris and the ciliary body and was then secreted into the aqueous and vitreous humors, where it accumulated as an active enzyme.


Subject(s)
Aqueous Humor/enzymology , Ciliary Body/enzymology , Intramolecular Oxidoreductases/metabolism , Iris/enzymology , Vitreous Body/enzymology , Animals , Blotting, Western , Female , Fluorescent Antibody Technique, Indirect , In Situ Hybridization , Intramolecular Oxidoreductases/genetics , Lens, Crystalline/enzymology , Lipocalins , Male , Mice , Mice, Inbred BALB C , Pigment Epithelium of Eye/enzymology , RNA, Messenger/metabolism , Rats , Rats, Sprague-Dawley
11.
J Neurosci ; 17(7): 2376-82, 1997 Apr 01.
Article in English | MEDLINE | ID: mdl-9065498

ABSTRACT

Glutathione-independent prostaglandin D synthase (PGDS) is an enzyme responsible for biosynthesis of prostaglandin D2 in the CNS and is identical to a major cerebrospinal fluid protein, beta-trace. Although PGDS has been identified recently in rat leptomeninges, little information is available about human meninges or meningiomas. Here, we report PGDS to be expressed consistently in 10 human arachnoid and arachnoid villi and in 21 meningiomas by immunohistochemistry, Western blot, and reverse transcription (RT)-PCR analyses. In arachnoid, PGDS immunoreactivity was seen in arachnoid barrier cells but was negligible in arachnoid trabecula and pia mater. In contrast, in arachnoid villi, PGDS was seen in core arachnoid cells rather than in the cap cell cluster or arachnoid cell layer. Meningioma cells also showed intense immunoreactivity in the perinuclear region, and it was often concentrated within meningocytic whorls and around calcifying psammoma bodies. Immunoelectron microscopic data, when compared with the ultrastructure, showed that PGDS was localized at rough endoplasmatic reticulum of arachnoid and meningioma cells. Western blot showed a 29 kDa immunoreactive band indicating PGDS, but the extent of expression was variable from case to case, which was compatible with immunohistochemical data. RT-PCR revealed PGDS gene expression in all meningiomas studied, regardless of histological subtypes, and also in human arachnoid villi. Because human arachnoid and meningioma cells exclusively express PGDS, it can be considered their specific cell marker. These results show functional differences in various types of meningeal cells attributable to differences in PGDS expression.


Subject(s)
Arachnoid/enzymology , Biomarkers, Tumor/analysis , Biomarkers/analysis , Calcinosis/enzymology , Intramolecular Oxidoreductases/analysis , Meningeal Neoplasms/enzymology , Meningioma/enzymology , Animals , Arachnoid/pathology , Arachnoid/ultrastructure , Calcinosis/pathology , Female , Humans , Immunohistochemistry , Intramolecular Oxidoreductases/cerebrospinal fluid , Lipocalins , Male , Meningeal Neoplasms/pathology , Meningeal Neoplasms/surgery , Meningeal Neoplasms/ultrastructure , Meningioma/pathology , Meningioma/surgery , Meningioma/ultrastructure , Microscopy, Immunoelectron , Microvilli/enzymology , Middle Aged , Rats , Reverse Transcriptase Polymerase Chain Reaction
12.
Cytotechnology ; 24(1): 11-7, 1997 May.
Article in English | MEDLINE | ID: mdl-22358592

ABSTRACT

Astrocytes, a member of the glial cell family in the central nervous system, are assumed to play a crucial role in the formation of the blood-brain barrier (BBB) in vertebrates. It was shown that astrocytes induce BBB-properties in brain capillary endothelial cells (BCEC) in vitro. We now established an astroglial cell line of non-tumoral origin. The cloned cell line (A7) shows a highly increased proliferation rate and expresses the astrocytic marker glial fibrillary acidic protein. Furthermore, the clone A7 expresses S-100-protein and vimentin, which are also expressed by primary cultured astrocytes. This cell line therefore shows general astrocytic features. In addition, we were able to show that A7 cells re-induce the BBB-related marker enzyme alkaline phosphatase in BCEC, when these two cell types are co-cultured. Thus we have a cell line which can be readily cultured in large quantities, shows common astrocyte properties and is able to influence BCEC with respect to a BBB-related feature.

13.
J Neurosci ; 16(19): 6119-24, 1996 Oct 01.
Article in English | MEDLINE | ID: mdl-8815894

ABSTRACT

Glutathione-Independent prostaglandin D synthase, identical to beta-trace, (a major CSF protein), is localized in the CNS. This enzyme, lipocalin-type prostaglandin D synthase, is a member of the lipocalin family of secretory proteins that transport small lipophilic substances. This enzyme's activity in adult rat retina was enriched sixfold in retinal pigment epithelium (RPE) and even more in interphotoreceptor matrix (IPM), all higher than brain. Western blots with anti-lipocalin-type prostaglandin D synthase showed three distinct immunoreactive bands. In the retinal cytosolic fraction, only one band was observed (M(r) 25,000); in IPM, the larger component occurred (M(r), 26,000). The RPE membrane-bound fraction showed two bands (M(r) 20,000 and 23,000), indicating synthesis, and the cytosolic fraction contained two bands (M(r) 23,000 and 26,000), indicating modification for release into IPM. At least two glycosylation sites occurred on the prostaglandin D synthase moiety, explaining the three immunoreactive bands in Western blots. Immunohistochemistry with polyclonal antibodies against this lipocalin-type enzyme showed intense localization in RPE, but less in photoreceptor outer and inner segments. In situ hybridization showed mRNA specifically expressed in RPE. Thus, lipocalin-type prostaglandin D synthase is predominantly expressed in RPE and actively accumulated in IPM. This may demonstrate gene sharing because, while catalyzing prostaglandin D2 synthesis, it may perform an additional, unrelated role in IPM. This enzyme is secreted from the RPE into IPM from which it is then taken up by photoreceptors. However, the nature of its ligand(s) is not known; they may be retinoids and/or docosahexanoic acid.


Subject(s)
Carrier Proteins/metabolism , Extracellular Matrix/enzymology , Intramolecular Oxidoreductases , Isomerases/metabolism , Photoreceptor Cells/enzymology , Pigment Epithelium of Eye/enzymology , Salivary Proteins and Peptides/metabolism , Animals , Blotting, Northern , Blotting, Western , Carrier Proteins/chemistry , Carrier Proteins/genetics , Female , Immunohistochemistry , In Situ Hybridization , Isomerases/chemistry , Isomerases/genetics , Lipocalin 1 , Lipocalins , Male , RNA, Messenger/metabolism , Rats , Rats, Sprague-Dawley , Retina/enzymology , Salivary Proteins and Peptides/chemistry , Salivary Proteins and Peptides/genetics , Tissue Distribution
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