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  • 1
    Online Resource
    Online Resource
    Elsevier BV ; 1990
    In:  Journal of Biological Chemistry Vol. 265, No. 22 ( 1990-08), p. 13118-13123
    In: Journal of Biological Chemistry, Elsevier BV, Vol. 265, No. 22 ( 1990-08), p. 13118-13123
    Type of Medium: Online Resource
    ISSN: 0021-9258
    Language: English
    Publisher: Elsevier BV
    Publication Date: 1990
    detail.hit.zdb_id: 2997-X
    SSG: 12
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  • 2
    Online Resource
    Online Resource
    European Respiratory Society (ERS) ; 2008
    In:  European Respiratory Journal Vol. 31, No. 5 ( 2008-01-09), p. 949-956
    In: European Respiratory Journal, European Respiratory Society (ERS), Vol. 31, No. 5 ( 2008-01-09), p. 949-956
    Type of Medium: Online Resource
    ISSN: 0903-1936 , 1399-3003
    Language: English
    Publisher: European Respiratory Society (ERS)
    Publication Date: 2008
    detail.hit.zdb_id: 639359-7
    detail.hit.zdb_id: 1499101-9
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  • 3
    Online Resource
    Online Resource
    Proceedings of the National Academy of Sciences ; 1994
    In:  Proceedings of the National Academy of Sciences Vol. 91, No. 8 ( 1994-04-12), p. 3275-3279
    In: Proceedings of the National Academy of Sciences, Proceedings of the National Academy of Sciences, Vol. 91, No. 8 ( 1994-04-12), p. 3275-3279
    Abstract: The Cl- secretory pathway that is defective in cystic fibrosis (CF) can be bypassed by an alternative pathway for Cl- transport that is activated by extracellular nucleotides. Accordingly, the P2 receptor that mediates this effect is a therapeutic target for improving Cl- secretion in CF patients. In this paper, we report the sequence and functional expression of a cDNA cloned from human airway epithelial (CF/T43) cells that encodes a protein with properties of a P2U nucleotide receptor. With a retrovirus system, the human airway clone was stably expressed in 1321N1 astrocytoma cells, a human cell line unresponsive to extracellular nucleotides. Studies of inositol phosphate accumulation and intracellular Ca2+ mobilization induced by extracellular nucleotides in 1321N1 cells expressing the receptor identified this clone as the target receptor in human airway epithelia. In addition, we independently isolated an identical cDNA from human colonic epithelial (HT-29) cells, indicating that this is the same P2U receptor that has been functionally identified in other human tissues. Expression of the human P2U receptor (HP2U) in 1321N1 cells revealed evidence for autocrine ATP release and stimulation of transduced receptors. Thus, HP2U expression in the 1321N1 cell line will be useful for studying autocrine regulatory mechanisms and in screening of potential therapeutic drugs.
    Type of Medium: Online Resource
    ISSN: 0027-8424 , 1091-6490
    RVK:
    RVK:
    Language: English
    Publisher: Proceedings of the National Academy of Sciences
    Publication Date: 1994
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    detail.hit.zdb_id: 1461794-8
    SSG: 11
    SSG: 12
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  • 4
    Online Resource
    Online Resource
    Proceedings of the National Academy of Sciences ; 1994
    In:  Proceedings of the National Academy of Sciences Vol. 91, No. 26 ( 1994-12-20), p. 13067-
    In: Proceedings of the National Academy of Sciences, Proceedings of the National Academy of Sciences, Vol. 91, No. 26 ( 1994-12-20), p. 13067-
    Type of Medium: Online Resource
    ISSN: 0027-8424 , 1091-6490
    RVK:
    RVK:
    Language: English
    Publisher: Proceedings of the National Academy of Sciences
    Publication Date: 1994
    detail.hit.zdb_id: 209104-5
    detail.hit.zdb_id: 1461794-8
    SSG: 11
    SSG: 12
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  • 5
    Online Resource
    Online Resource
    American Physiological Society ; 1995
    In:  American Journal of Physiology-Cell Physiology Vol. 268, No. 2 ( 1995-02-01), p. C425-C433
    In: American Journal of Physiology-Cell Physiology, American Physiological Society, Vol. 268, No. 2 ( 1995-02-01), p. C425-C433
    Abstract: Luminal extracellular ATP evoked a bumetanide-sensitive short-circuit current in cultured T84 cell epithelia (90.2 +/- 18.2 microA/cm2 at 100 microM ATP, apparent 50% effective concentration, 11.5 microM). ATP appeared to increase the Cl- conductance of the apical membrane but not the driving force for Cl- secretion determined by basolateral membrane K+ conductance. Specifically, the magnitude of Cl- secretion stimulated by ATP was independent of basal current, and forskolin pretreatment abolished subsequent stimulation of Cl- secretion by ATP. Whereas ATP stimulated modest production of adenosine 3',5'-cyclic monophosphate (cAMP) by T84 cells, ATP caused smaller increases in intracellular Ca2+ and inositol phosphate activities than the Ca(2+)-signaling Cl- secretagogue carbachol. An inhibitor of 5'-nucleotidase, alpha,beta-methyleneadenosine 5'-diphosphate, blocked most of the response to luminal ATP. The adenosine receptor antagonist 8-(p-sulfophenyl)theophylline blocked both the luminal ATP-dependent generation of cAMP and Cl- secretion when administered to the luminal but not submucosal bath. These results demonstrate that the Cl- secretion stimulated by luminal ATP is mediated by a A2-adenosine receptor located on the apical cell membrane. Thus metabolism of extracellular ATP to adenosine regulates the activity of cystic fibrosis transmembrane conductor regulator (CFTR) in the apical membrane of polarized T84 cells.
    Type of Medium: Online Resource
    ISSN: 0363-6143 , 1522-1563
    Language: English
    Publisher: American Physiological Society
    Publication Date: 1995
    detail.hit.zdb_id: 1477334-X
    detail.hit.zdb_id: 392098-7
    SSG: 12
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  • 6
    Online Resource
    Online Resource
    Wiley ; 1996
    In:  Journal of Autonomic Pharmacology Vol. 16, No. 6 ( 1996-12), p. 319-324
    In: Journal of Autonomic Pharmacology, Wiley, Vol. 16, No. 6 ( 1996-12), p. 319-324
    Type of Medium: Online Resource
    ISSN: 0144-1795 , 1365-2680
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 1996
    detail.hit.zdb_id: 2020425-5
    detail.hit.zdb_id: 604626-5
    SSG: 15,3
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  • 7
    Online Resource
    Online Resource
    American Physiological Society ; 1994
    In:  American Journal of Physiology-Cell Physiology Vol. 266, No. 2 ( 1994-02-01), p. C406-C415
    In: American Journal of Physiology-Cell Physiology, American Physiological Society, Vol. 266, No. 2 ( 1994-02-01), p. C406-C415
    Abstract: The effect of purinergic receptor agonists on arachidonic acid release was investigated in [3H]arachidonic acid-prelabeled human airway epithelial cells. Exposure of bronchial epithelial BEAS39 cells to extracellular ATP resulted in a marked release of unesterified [3H] arachidonic acid with maximal effect observed within 60-90 s. [3H]diacylglycerol and [3H] phosphatidic acid accumulated in parallel with [3H]arachidonic acid. ATP-stimulated [3H] arachidonic acid release with a K0.5 of 9 +/- 2 microM and UTP was equipotent; no effect was observed with P2Y- or P2X-purinergic receptor agonists or with adenosine. Similar results were obtained with primary cultures of normal human nasal epithelium, CF/T43 and HBE1 airway epithelial cell lines derived from a cystic fibrosis patient and from a normal donor, respectively, and HT-29 human colon carcinoma cells. ATP stimulated inositol phosphate formation in BEAS39 cells with a concentration dependence identical to that for [3H]arachidonic acid release. The effect of ATP on both [3H] arachidonic acid release and inositol phosphate formation was equally inhibited by pertussis toxin. The Ca2+ ionophore A-23187 mimicked the effects of ATP or UTP on arachidonic acid release, and a marked inhibitory effect was observed with thapsigargin. The protein kinase C inhibitor staurosporine partially inhibited ATP-stimulated [3H]arachidonic acid release. These data are consistent with the hypothesis that phospholipase A2 activation is secondary to P2U-purinergic receptor stimulation of D-myoinositol 1,4,5-trisphosphate production and calcium mobilization from intracellular stores.
    Type of Medium: Online Resource
    ISSN: 0363-6143 , 1522-1563
    Language: English
    Publisher: American Physiological Society
    Publication Date: 1994
    detail.hit.zdb_id: 1477334-X
    detail.hit.zdb_id: 392098-7
    SSG: 12
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  • 8
    Online Resource
    Online Resource
    Wiley ; 2010
    In:  Acta Physiologica Vol. 199, No. 2 ( 2010-06), p. 149-160
    In: Acta Physiologica, Wiley, Vol. 199, No. 2 ( 2010-06), p. 149-160
    Abstract: The P2Y 14 receptor is a relatively broadly expressed G protein‐coupled receptor that is prominently associated with immune and inflammatory cells as well as with many epithelia. This receptor historically was thought to be activated selectively by UDP‐glucose and other UDP‐sugars. However, UDP is also a very potent agonist of this receptor, and may prove to be one of its most important cognate activators.
    Type of Medium: Online Resource
    ISSN: 1748-1708 , 1748-1716
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2010
    detail.hit.zdb_id: 2219379-0
    detail.hit.zdb_id: 2218636-0
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  • 9
    Online Resource
    Online Resource
    Wiley ; 2008
    In:  British Journal of Pharmacology Vol. 153, No. 7 ( 2008-04), p. 1528-1537
    In: British Journal of Pharmacology, Wiley, Vol. 153, No. 7 ( 2008-04), p. 1528-1537
    Abstract: The P2Y 14 receptor is activated by UDP‐sugars, most potently by UDP‐glucose, but not by free nucleotides, suggesting that UDP‐glucose is the cognate agonist for this receptor. However, evidence for regulated release of UDP‐glucose is scarce. In the present study, the occurrence of receptor‐promoted release of UDP‐glucose was investigated, using 1321N1 human astrocytoma cells. Experimental approach: UDP‐glucose release and hydrolysis were measured using HPLC‐based techniques. Phospholipase C activation and actin cytoskeleton reorganization were assessed by measuring inositol phosphate formation and fluorescence confocal microscopy, respectively. Key results: Thrombin and the protease‐activating receptor‐1 (PAR1) peptide TFLLRNPNDK (PAR1‐AP) evoked the release of UDP‐glucose and ATP, which was accompanied by enhanced inositol phosphate formation. Although carbachol promoted fourfold greater inositol phosphate formation than thrombin, it failed to promote nucleotide release. Thrombin‐promoted nucleotide release was inhibited by BAPTA‐AM, brefeldin A and cytochalasin D, and was insensitive to Pertussis toxin and PI3‐kinase inhibitors. Thrombin, but not carbachol, induced actin cytoskeleton reorganization, a hallmark of Rho activation in 1321N1 cells. However, PAR‐promoted UDP‐glucose release was not affected by Rho kinase inhibition. Conclusions and implications: PAR1‐evoked UDP‐glucose release reflected a Ca 2+ ‐dependent mechanism, engaging additional signalling independently of G i and Rho kinase activation and requiring a functional actin cytoskeleton and Golgi structures. Our study demonstrates the occurrence of Ca 2+ ‐dependent release of UDP‐glucose from astrocytoma cells in response to a physiologically relevant stimulus, that is, a G‐protein‐coupled receptor agonist. Given the presence of P2Y 14 receptors in astrocytes, UDP‐glucose may have important autocrine/paracrine functions in the brain. British Journal of Pharmacology (2008) 153 , 1528–1537; doi: 10.1038/sj.bjp.0707692 ; published online 21 January 2008
    Type of Medium: Online Resource
    ISSN: 0007-1188 , 1476-5381
    Language: English
    Publisher: Wiley
    Publication Date: 2008
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    detail.hit.zdb_id: 2029728-2
    SSG: 15,3
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  • 10
    In: Animal Behavior and Cognition, Animal Behavior and Cognition, Vol. 10, No. 3 ( 2023-08-01), p. 232-286
    Abstract: To promote collaboration across canine science, address replicability issues, and advance open science practices within animal cognition, we have launched the ManyDogs consortium, modeled on similar ManyX projects in other fields. We aimed to create a collaborative network that (a) uses large, diverse samples to investigate and replicate findings, (b) promotes open science practices of pre-registering hypotheses, methods, and analysis plans, (c) investigates the influence of differences across populations and breeds, and (d) examines how different research methods and testing environments influence the robustness of results. Our first study combines a phenomenon that appears to be highly reliable—dogs’ ability to follow human pointing—with a question that remains controversial: do dogs interpret pointing as a social communicative gesture or as a simple associative cue? We collected data (N = 455) from 20 research sites on two conditions of a 2-alternative object choice task: (1) Ostensive (pointing to a baited cup after making eye-contact and saying the dog’s name); (2) Non-ostensive (pointing without eye-contact, after a throat-clearing auditory control cue). Comparing performance between conditions, while both were significantly above chance, there was no significant difference in dogs’ responses. This result was consistent across sites. Further, we found that dogs followed contralateral, momentary pointing at lower rates than has been reported in prior research, suggesting that there are limits to the robustness of point-following behavior: not all pointing styles are equally likely to elicit a response. Together, these findings underscore the important role of procedural details in study design and the broader need for replication studies in canine science.
    Type of Medium: Online Resource
    ISSN: 2372-4323
    URL: Issue
    Language: Unknown
    Publisher: Animal Behavior and Cognition
    Publication Date: 2023
    detail.hit.zdb_id: 2933480-9
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