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  1 / 23825 MEDLINE  
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[PMID]:23269784
[Au] Autor:Hussmann KL; Samuel MA; Kim KS; Diamond MS; Fredericksen BL
[Ad] Endereço:Department of Cell Biology and Molecular Genetics, University of Maryland College Park, College Park, Maryland, USA.
[Ti] Título:Differential replication of pathogenic and nonpathogenic strains of West Nile virus within astrocytes.
[So] Source:J Virol;87(5):2814-22, 2013 Mar.
[Is] ISSN:1098-5514
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:The severity of West Nile virus (WNV) infection in immunocompetent animals is highly strain dependent, ranging from avirulent to highly neuropathogenic. Here, we investigate the nature of this strain-specific restriction by analyzing the replication of avirulent (WNV-MAD78) and highly virulent (WNV-NY) strains in neurons, astrocytes, and microvascular endothelial cells, which comprise the neurovascular unit within the central nervous system (CNS). We demonstrate that WNV-MAD78 replicated in and traversed brain microvascular endothelial cells as efficiently as WNV-NY. Likewise, similar levels of replication were detected in neurons. Thus, WNV-MAD78's nonneuropathogenic phenotype is not due to an intrinsic inability to replicate in key target cells within the CNS. In contrast, replication of WNV-MAD78 was delayed and reduced compared to that of WNV-NY in astrocytes. The reduced susceptibility of astrocytes to WNV-MAD78 was due to a delay in viral genome replication and an interferon-independent reduction in cell-to-cell spread. Together, our data suggest that astrocytes regulate WNV spread within the CNS and therefore are an attractive target for ameliorating WNV-induced neuropathology.
[Mh] Termos MeSH primário: Astrócitos/virologia
Células Endoteliais/virologia
Replicação Viral
Vírus do Nilo Ocidental/fisiologia
[Mh] Termos MeSH secundário: Animais
Linhagem Celular
Sistema Nervoso Central/virologia
Cercopithecus aethiops
Humanos
Microvasos/citologia
Microvasos/virologia
Neurônios/virologia
Células Vero
Febre do Nilo Ocidental/transmissão
Febre do Nilo Ocidental/virologia
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, N.I.H., EXTRAMURAL; RESEARCH SUPPORT, U.S. GOV'T, NON-P.H.S.
[Em] Mês de entrada:1304
[Cu] Atualização por classe:130513
[Lr] Data última revisão:
130513
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:130212
[St] Status:MEDLINE
[do] DOI:10.1128/JVI.02577-12


  2 / 23825 MEDLINE  
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[PMID]:23233794
[Au] Autor:Hong S; Iizuka Y; Kim CY; Seong GJ
[Ad] Endereço:Institute of Vision Research, Department of Ophthalmology, Yonsei University College of Medicine, Seoul, Korea. samini@yuhs.ac
[Ti] Título:Isolation of primary mouse retinal ganglion cells using immunopanning-magnetic separation.
[So] Source:Mol Vis;18:2922-30, 2012.
[Is] ISSN:1090-0535
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:PURPOSE: To establish an effective system for isolating primary retinal ganglion cells (RGCs) from newborn mice. METHODS: The retinas were separated from enucleated eyeballs of Crl:CD-1 mice on postnatal day 1 to 4. RGCs were purified using three different methods, including two-step immunopanning (TSI), direct magnetic separation (DMS), and immunopanning-magnetic separation (IMS). Harvested cells were maintained for 24 h in a defined medium and then examined with immunocytochemistry, western immunoblotting, and real-time reverse transcription polymerase chain reaction (RT-PCR) for glial cell-specific glial fibrillary acidic protein (GFAP) and amacrine cell-specific syntaxin 1. RESULTS: As determined with immunofluorescence staining, RGCs purified by TSI were sparsely mixed with GFAP-positive astrocytes, and RGCs isolated by DMS were frequently mixed with syntaxin 1-positive amacrine cells. However, RGCs collected by IMS were seldom contaminated by GFAP-positive or syntaxin 1-positive cells. On western immunoblots, TSI cells showed significant GFAP expression, and DMS cells showed apparent syntaxin 1 expression, but IMS cells did not. Results of the real-time RT-PCR showed a similar tendency to those of the immunocytochemistry and western immunoblots. CONCLUSION: Primary mouse RGCs were highly purified by the IMS method, combining the benefits of the TSI and DMS methods. This isolation method may provide a good experimental system for studying glaucoma in vitro.
[Mh] Termos MeSH primário: Separação Imunomagnética/métodos
Células Ganglionares da Retina/citologia
[Mh] Termos MeSH secundário: Células Amácrinas/citologia
Células Amácrinas/metabolismo
Animais
Animais Recém-Nascidos
Anticorpos/química
Anticorpos/imunologia
Astrócitos/citologia
Astrócitos/metabolismo
Marcadores Biológicos/metabolismo
Western Blotting
Feminino
Expressão Gênica
Imunoistoquímica
Separação Imunomagnética/normas
Camundongos
Proteínas do Tecido Nervoso/genética
Proteínas do Tecido Nervoso/metabolismo
Cultura Primária de Células
Reação em Cadeia da Polimerase em Tempo Real
Células Ganglionares da Retina/metabolismo
Sintaxina 1/genética
Sintaxina 1/metabolismo
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T
[Nm] Nome de substância:
0 (Antibodies); 0 (Biological Markers); 0 (Nerve Tissue Proteins); 0 (Syntaxin 1); 0 (glial fibrillary astrocytic protein, mouse)
[Em] Mês de entrada:1305
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:121212
[St] Status:MEDLINE


  3 / 23825 MEDLINE  
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[PMID]:23041616
[Au] Autor:Radzishevsky I; Sason H; Wolosker H
[Ad] Endereço:Department of Biochemistry, B Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa, Israel.
[Ti] Título:D-serine: physiology and pathology.
[So] Source:Curr Opin Clin Nutr Metab Care;16(1):72-5, 2013 Jan.
[Is] ISSN:1473-6519
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:PURPOSE OF REVIEW: Here, we discuss the recent data on the role of different N-methyl D-aspartate receptor (NMDAR) coagonists, D-serine and glycine, in regulating NMDAR activity and neurotoxicity. RECENT FINDINGS: D-Serine originates from both neurons and astrocytes, from where it is released by different mechanisms. Recent data indicate that like glial D-serine, neuronal D-serine is required for NMDAR-dependent, long-term potentiation at the hippocampal CA1-CA3 synapses and proper synapse formation in the cerebral cortex. D-serine is the physiological coagonist of synaptic NMDAR, whereas glycine action is restricted to extrasynaptic sites. SUMMARY: D-Serine is now recognized as the major NMDAR coagonist at the synapse. The data establish D-serine as a key transmitter or neuromodulator that mediates synaptic NMDAR activation and neurotoxicity. In this context, drugs that inhibit D-serine synthesis or release will provide new neuroprotective strategy.
[Mh] Termos MeSH primário: Glicina/fisiologia
Receptores de N-Metil-D-Aspartato/fisiologia
Serina/fisiologia
[Mh] Termos MeSH secundário: Animais
Astrócitos/fisiologia
Hipocampo/fisiologia
Humanos
Potenciação de Longa Duração
Modelos Animais
Neurônios/fisiologia
Síndromes Neurotóxicas/patologia
Sinapses/fisiologia
Transmissão Sináptica
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T; REVIEW
[Nm] Nome de substância:
0 (Receptors, N-Methyl-D-Aspartate); 56-40-6 (Glycine); 56-45-1 (Serine)
[Em] Mês de entrada:1305
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:121210
[St] Status:MEDLINE
[do] DOI:10.1097/MCO.0b013e32835a3466


  4 / 23825 MEDLINE  
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[PMID]:23185276
[Au] Autor:Chander BS; Chakravarthy VS
[Ad] Endereço:Department of Biotechnology, Indian Institute of Technology, Madras, Chennai, India.
[Ti] Título:A computational model of neuro-glio-vascular loop interactions.
[So] Source:PLoS One;7(11):e48802, 2012.
[Is] ISSN:1932-6203
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:We present a computational, biophysical model of neuron-astrocyte-vessel interaction. Unlike other cells, neurons convey "hunger" signals to the vascular network via an intervening layer of glial cells (astrocytes); vessels dilate and release glucose which fuels neuronal firing. Existing computational models focus on only parts of this loop (neuron→astrocyte→vessel→neuron), whereas the proposed model describes the entire loop. Neuronal firing causes release of a neurotransmitter like glutamate which triggers release of vasodilator by astrocytes via a cascade of biochemical events. Vasodilators released from astrocytic endfeet cause blood vessels to dilate and release glucose into the interstitium, part of which is taken up by the astrocyticendfeet. Glucose is converted into lactate in the astrocyte and transported into the neuron. Glucose from the interstitium and lactate (produced from glucose) influx from astrocyte are converted into ATP in the neuron. Neuronal ATP is used to drive the Na(+)/K(+)ATPase pumps, which maintain ionic gradients necessary for neuronal firing. When placed in the metabolic loop, the neuron exhibits sustained firing only when the stimulation current is more than a minimum threshold. For various combinations of initial neuronal [ATP] and external current, the neuron exhibits a variety of firing patterns including sustained firing, firing after an initial pause, burst firing etc. Neurovascular interactions under conditions of constricted vessels are also studied. Most models of cerebral circulation describe neurovascular interactions exclusively in the "forward" neuron→vessel direction. The proposed model indicates possibility of "reverse" influence also, with vasomotion rhythms influencing neural firing patterns. Another idea that emerges out of the proposed work is that brain's computations may be more comprehensively understood in terms of neuro-glial-vascular dynamics and not in terms of neural firing alone.
[Mh] Termos MeSH primário: Vasos Sanguíneos/fisiologia
Simulação por Computador
Retroalimentação Fisiológica
Modelos Neurológicos
Neuroglia/fisiologia
Neurônios/fisiologia
[Mh] Termos MeSH secundário: Potenciais de Ação/fisiologia
Trifosfato de Adenosina/metabolismo
Astrócitos/metabolismo
Canais de Potássio/metabolismo
Transdução de Sinal
Canais de Sódio/metabolismo
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T
[Nm] Nome de substância:
0 (Potassium Channels); 0 (Sodium Channels); 56-65-5 (Adenosine Triphosphate)
[Em] Mês de entrada:1305
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:121127
[St] Status:MEDLINE
[do] DOI:10.1371/journal.pone.0048802


  5 / 23825 MEDLINE  
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[PMID]:22967085
[Au] Autor:Braganza O; Bedner P; Hüttmann K; von Staden E; Friedman A; Seifert G; Steinhäuser C
[Ad] Endereço:Institute of Cellular Neurosciences, University of Bonn, Sigmund Freud Strasse 25, Bonn, Germany.
[Ti] Título:Albumin is taken up by hippocampal NG2 cells and astrocytes and decreases gap junction coupling.
[So] Source:Epilepsia;53(11):1898-906, 2012 Nov.
[Is] ISSN:1528-1167
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:PURPOSE: Dysfunction of the blood-brain barrier (BBB) and albumin extravasation have been suggested to play a role in the etiology of human epilepsy. In this context, dysfunction of glial cells attracts increasing attention. Our study was aimed to analyze in the hippocampus (1) which cell types internalize albumin injected into the lateral ventricle in vivo, (2) whether internalization into astrocytes impacts their coupling and expression of connexin 43 (Cx43), and (3) whether expression of Kir4.1, the predominating astrocytic K(+) channel subunit, is altered by albumin. METHODS: The patch-clamp method was combined with single cell tracer filling to investigate electrophysiologic properties and gap junction coupling (GJC). For cell identification, mice with cell type-specific expression of a fluorescent protein (NG2kiEYFP mice) and immunohistochemistry were employed. Semiquantitative real time polymerase chain reaction (RT-PCR) allowed analysis of Kir4.1 and Cx43 transcript levels. KEY FINDINGS: We show that fluorescently labeled albumin is taken up by astrocytes, NG2 cells, and neurons, with NG2 cells standing out in terms of the quantity of uptake. Within 5 days postinjection (dpi), intracellular albumin accumulation was largely reduced suggesting rapid degradation. Electrophysiologic analysis of astrocytes and NG2 cells revealed no changes in their membrane properties at either time point. However, astrocytic GJC was significantly decreased at 1 dpi but returned to control levels within 5 dpi. We found no changes in hippocampal Cx43 transcript expression, suggesting that other mechanisms account for the observed changes in coupling. Kir4.1 mRNA was regulated oppositely in the CA1 stratum radiatum, with a strong increase at 1 dpi followed by a decrease at 5 dpi. SIGNIFICANCE: The present study demonstrates that extravasal albumin in the hippocampus induces rapid changes of astrocyte function, which can be expected to impair ion and transmitter homeostasis and contribute to hyperactivity and epileptogenesis. Therefore, astrocytes may represent alternative targets for antiepileptic therapeutic approaches.
[Mh] Termos MeSH primário: Astrócitos/metabolismo
Junções Gap/metabolismo
Hipocampo/metabolismo
Albumina Sérica/fisiologia
[Mh] Termos MeSH secundário: Animais
Astrócitos/patologia
Corantes Fluorescentes/administração & dosagem
Corantes Fluorescentes/metabolismo
Junções Gap/patologia
Hipocampo/efeitos de drogas
Hipocampo/patologia
Injeções Intraventriculares
Camundongos
Camundongos Endogâmicos C57BL
Camundongos Transgênicos
Albumina Sérica/administração & dosagem
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T
[Nm] Nome de substância:
0 (Fluorescent Dyes); 0 (Serum Albumin)
[Em] Mês de entrada:1301
[Cu] Atualização por classe:130513
[Lr] Data última revisão:
130513
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:121113
[St] Status:MEDLINE
[do] DOI:10.1111/j.1528-1167.2012.03665.x


  6 / 23825 MEDLINE  
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[PMID]:23104556
[Au] Autor:Rothman DL; De Feyter HM; Maciejewski PK; Behar KL
[Ad] Endereço:Department of Diagnostic Radiology and Biomedical Engineering, Magnetic Resonance Research Center, Yale University School of Medicine, 300 Cedar Street, P.O. Box 208043, New Haven, CT 06520-8043, USA. douglas.rothman@yale.edu
[Ti] Título:Is there in vivo evidence for amino acid shuttles carrying ammonia from neurons to astrocytes?
[So] Source:Neurochem Res;37(11):2597-612, 2012 Nov.
[Is] ISSN:1573-6903
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:The high in vivo flux of the glutamate/glutamine cycle puts a strong demand on the return of ammonia released by phosphate activated glutaminase from the neurons to the astrocytes in order to maintain nitrogen balance. In this paper we review several amino acid shuttles that have been proposed for balancing the nitrogen flows between neurons and astrocytes in the glutamate/glutamine cycle. All of these cycles depend on the directionality of glutamate dehydrogenase, catalyzing reductive glutamate synthesis (forward reaction) in the neuron in order to capture the ammonia released by phosphate activated glutaminase, while catalyzing oxidative deamination of glutamate (reverse reaction) in the astrocytes to release ammonia for glutamine synthesis. Reanalysis of results from in vivo experiments using (13)N and (15)N labeled ammonia and (15)N leucine in rats suggests that the maximum flux of the alanine/lactate or branched chain amino acid/branched chain amino acid transaminase shuttles between neurons and astrocytes are approximately 3-5 times lower than would be required to account for the ammonia transfer from neurons to astrocytes needed for glutamine synthesis (amide nitrogen) to sustain the glutamate/glutamine cycle. However, in the rat brain both the total ammonia fixation rate by glutamate dehydrogenase and the total branched chain amino acid transaminase activity are sufficient to support a branched chain amino acid/branched chain keto acid shuttle, as proposed by Hutson and coworkers, which would support the de novo synthesis of glutamine in the astrocyte to replace the ~20 % of neurotransmitter glutamate that is oxidized. A higher fraction of the nitrogen needs of total glutamate neurotransmitter cycling could be supported by hybrid cycles in which glutamate and tricarboxylic acid cycle intermediates act as a nitrogen shuttle. A limitation of all in vivo studies in animals conducted to date is that none have shown transfer of nitrogen for glutamine amide synthesis, either as free ammonia or via an amino acid from the neurons to the astrocytes. Future work will be needed, perhaps using methods for selectively labeling nitrogen in neurons, to conclusively establish the rate of amino acid nitrogen shuttles in vivo and their coupling to the glutamate/glutamine cycle.
[Mh] Termos MeSH primário: Aminoácidos/metabolismo
Amônia/metabolismo
Astrócitos/metabolismo
Neurônios/metabolismo
[Mh] Termos MeSH secundário: Animais
Transporte Biológico
Humanos
Nitrogênio/metabolismo
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, N.I.H., EXTRAMURAL; RESEARCH SUPPORT, NON-U.S. GOV'T; REVIEW
[Nm] Nome de substância:
0 (Amino Acids); 7664-41-7 (Ammonia); 7727-37-9 (Nitrogen)
[Em] Mês de entrada:1304
[Cu] Atualização por classe:130513
[Lr] Data última revisão:
130513
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:121105
[St] Status:MEDLINE
[do] DOI:10.1007/s11064-012-0898-7


  7 / 23825 MEDLINE  
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[PMID]:23029249
[Au] Autor:Vandergaast R; Fredericksen BL
[Ad] Endereço:Department of Cell Biology and Molecular Genetics University of Maryland, College Park, MD, USA.
[Ti] Título:West Nile virus (WNV) replication is independent of autophagy in mammalian cells.
[So] Source:PLoS One;7(9):e45800, 2012.
[Is] ISSN:1932-6203
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:Autophagy is a homeostatic process responsible for recycling cytosolic proteins and organelles. Moreover, this pathway contributes to the cell's intrinsic innate defenses. While many viruses have evolved mechanisms to antagonize the antiviral effects of the autophagy pathway, others subvert autophagy to facilitate replication. Here, we have investigated the role of autophagy in West Nile virus (WNV) replication. Experiments in cell lines derived from a variety of sources, including the kidney, liver, skin, and brain, indicated that WNV replication does not upregulate the autophagy pathway. Furthermore, WNV infection did not inhibit rapamycin-induced autophagy, suggesting that WNV does not disrupt the authophagy signaling cascade. Perturbation of the autophagy pathway by depletion of the major autophagy factors Atg5 or Atg7 had no effect on WNV infectious particle production, indicating that WNV does not require a functional autophagy pathway for replication. Taken together, the results of our study provide evidence that WNV, unlike several other viruses of the family Flaviviridae, does not significantly interact with the conventional autophagy pathway in mammalian cells.
[Mh] Termos MeSH primário: Autofagia
Replicação Viral
Vírus do Nilo Ocidental/fisiologia
[Mh] Termos MeSH secundário: Animais
Astrócitos/metabolismo
Astrócitos/fisiologia
Astrócitos/virologia
Cercopithecus aethiops
Fibroblastos/metabolismo
Fibroblastos/fisiologia
Fibroblastos/virologia
Técnicas de Silenciamento de Genes
Células HEK293
Interações Hospedeiro-Patógeno
Humanos
Proteínas Associadas aos Microtúbulos/genética
Proteínas Associadas aos Microtúbulos/metabolismo
Cultura Primária de Células
Interferência de RNA
Proteínas de Ligação a RNA/metabolismo
Vírus Sindbis/fisiologia
Células Vero
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, N.I.H., EXTRAMURAL
[Nm] Nome de substância:
0 (ATG5 protein, human); 0 (MAP1LC3B protein, human); 0 (Microtubule-Associated Proteins); 0 (P62 protein, human); 0 (RNA-Binding Proteins)
[Em] Mês de entrada:1302
[Cu] Atualização por classe:130513
[Lr] Data última revisão:
130513
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:121002
[St] Status:MEDLINE
[do] DOI:10.1371/journal.pone.0045800


  8 / 23825 MEDLINE  
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[PMID]:22573306
[Au] Autor:Hegyi Z; Holló K; Kis G; Mackie K; Antal M
[Ad] Endereço:Department of Anatomy, Histology and Embryology, Faculty of Medicine, Medical and Health Science Center, University of Debrecen, Debrecen, Hungary.
[Ti] Título:Differential distribution of diacylglycerol lipase-alpha and N-acylphosphatidylethanolamine-specific phospholipase d immunoreactivity in the superficial spinal dorsal horn of rats.
[So] Source:Glia;60(9):1316-29, 2012 Sep.
[Is] ISSN:1098-1136
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:It is generally accepted that the endocannabinoid system plays important roles in spinal pain processing. Although it is documented that cannabinoid-1 receptors are strongly expressed in the superficial spinal dorsal horn, the cellular distribution of enzymes that can synthesize endocannabinoid ligands is less well studied. Thus, using immunocytochemical methods at the light and electron microscopic levels, we investigated the distribution of diacylglycerol lipase-alpha (DGL-α) and N-acylphosphatidylethanolamine-specific phospholipase D (NAPE-PLD), enzymes synthesizing the endocannabinoid ligands, 2-arachidonoylglycerol (2-AG) and anandamide, respectively. Positive labeling was revealed only occasionally in axon terminals, but dendrites displayed strong immunoreactivity for both enzymes. However, the dendritic localization of DGL-α and NAPE-PLD showed a remarkably different distribution. DGL-α immunolabeling in dentrites was always revealed at membrane compartments in close vicinity to synapses. In contrast to this, dendritic NAPE-PLD labeling was never observed in association with synaptic contacts. In addition to dendrites, a substantial proportion of astrocytic (immunoreactive for GFAP) and microglial (immunoreactive for CD11b) profiles were also immunolabeled for both DGL-α and NAPE-PLD. Glial processes immunostained for DGL-α were frequently found near to synapses in which the postsynaptic dendrite was immunoreactive for DGL-α, whereas NAPE-PLD immunoreactivity on glial profiles at the vicinity of synapses was only occasionally observed. Our results suggest that both neurons and glial cells can synthesize and release 2-AG and anandamide in the superficial spinal dorsal horn. The 2-AG can primarily be released by postsynaptic dendrites and glial processes adjacent to synapses, whereas anandamide can predominantly be released from nonsynaptic dendritic and glial compartments.
[Mh] Termos MeSH primário: Astrócitos/enzimologia
Lipase Lipoproteica/metabolismo
Microglia/enzimologia
Fosfolipase D/metabolismo
Medula Espinal/enzimologia
[Mh] Termos MeSH secundário: Animais
Astrócitos/ultraestrutura
Dendritos/enzimologia
Dendritos/ultraestrutura
Microglia/ultraestrutura
Neurônios/enzimologia
Neurônios/ultraestrutura
Ratos
Ratos Endogâmicos WKY
Medula Espinal/ultraestrutura
Sinapses/enzimologia
Sinapses/ultraestrutura
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T
[Nm] Nome de substância:
EC 3.1.1.34 (Lipoprotein Lipase); EC 3.1.4.4 (NAPE-PLD protein, rat); EC 3.1.4.4 (Phospholipase D)
[Em] Mês de entrada:1301
[Cu] Atualização por classe:130513
[Lr] Data última revisão:
130513
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:120719
[St] Status:MEDLINE
[do] DOI:10.1002/glia.22351


  9 / 23825 MEDLINE  
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[PMID]:23224430
[Au] Autor:Kreft M; Luksic M; Zorec TM; Prebil M; Zorec R
[Ad] Endereço:LN-MCP, Faculty of Medicine, Institute of Pathophysiology, University of Ljubljana, Zaloska cesta 4, 1000, Ljubljana, Slovenia. marko.kreft@bf.uni-lj.si
[Ti] Título:Diffusion of D-glucose measured in the cytosol of a single astrocyte.
[So] Source:Cell Mol Life Sci;70(8):1483-92, 2013 Apr.
[Is] ISSN:1420-9071
[Cp] País de publicação:Switzerland
[La] Idioma:eng
[Ab] Resumo:Astrocytes interact with neurons and endothelial cells and may mediate exchange of metabolites between capillaries and nerve terminals. In the present study, we investigated intracellular glucose diffusion in purified astrocytes after local glucose uptake. We used a fluorescence resonance energy transfer (FRET)-based nano sensor to monitor the time dependence of the intracellular glucose concentration at specific positions within the cell. We observed a delay in onset and kinetics in regions away from the glucose uptake compared with the region where we locally super-fused astrocytes with the D-glucose-rich solution. We propose a mathematical model of glucose diffusion in astrocytes. The analysis showed that after gradual uptake of glucose, the locally increased intracellular glucose concentration is rapidly spread throughout the cytosol with an apparent diffusion coefficient (D app) of (2.38 ± 0.41) × 10(-10) m(2) s(-1) (at 22-24 °C). Considering that the diffusion coefficient of D-glucose in water is D = 6.7 × 10(-10) m(2) s(-1) (at 24 °C), D app determined in astrocytes indicates that the cytosolic tortuosity, which hinders glucose molecules, is approximately three times higher than in aqueous solution. We conclude that the value of D app for glucose measured in purified rat astrocytes is consistent with the view that cytosolic diffusion may allow glucose and glucose metabolites to traverse from the endothelial cells at the blood-brain barrier to neurons and neighboring astrocytes.
[Mh] Termos MeSH primário: Astrócitos/metabolismo
Citossol/metabolismo
Glucose/metabolismo
[Mh] Termos MeSH secundário: Animais
Transporte Biológico
Células Cultivadas
Difusão
Transferência Ressonante de Energia de Fluorescência
Cinética
Modelos Biológicos
Ratos
Análise de Célula Única
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T
[Nm] Nome de substância:
50-99-7 (Glucose)
[Em] Mês de entrada:1305
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:130326
[St] Status:MEDLINE
[do] DOI:10.1007/s00018-012-1219-7


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[PMID]:22883744
[Au] Autor:Cudaback E; Li X; Yang Y; Yoo T; Montine KS; Craft S; Montine TJ; Keene CD
[Ad] Endereço:Department of Pathology, University of Washington, Seattle, WA 98104, USA.
[Ti] Título:Apolipoprotein C-I is an APOE genotype-dependent suppressor of glial activation.
[So] Source:J Neuroinflammation;9:192, 2012.
[Is] ISSN:1742-2094
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:BACKGROUND: Inheritance of the human ε4 allele of the apolipoprotein (apo) E gene (APOE) significantly increases the risk of developing Alzheimer's disease (AD), in addition to adversely influencing clinical outcomes of other neurologic diseases. While apoE isoforms differentially interact with amyloid ß (Aß), a pleiotropic neurotoxin key to AD etiology, more recent work has focused on immune regulation in AD pathogenesis and on the mechanisms of innate immunomodulatory effects associated with inheritance of different APOE alleles. APOE genotype modulates expression of proximal genes including APOC1, which encodes a small apolipoprotein that is associated with Aß plaques. Here we tested the hypothesis that APOE-genotype dependent innate immunomodulation may be mediated in part by apoC-I. METHODS: ApoC-I concentration in cerebrospinal fluid from control subjects of differing APOE genotypes was quantified by ELISA. Real-time PCR and ELISA were used to analyze apoC-I mRNA and protein expression, respectively, in liver, serum, cerebral cortex, and cultured primary astrocytes derived from mice with targeted replacement of murine APOE for human APOE ε3 or ε4. ApoC-I direct modulation of innate immune activity was investigated in cultured murine primary microglia and astrocytes, as well as human differentiated macrophages, using specific toll-like receptor agonists LPS and PIC as well as Aß. RESULTS: ApoC-I levels varied with APOE genotype in humans and in APOE targeted replacement mice, with ε4 carriers showing significantly less apoC-I in both species. ApoC-I potently reduced pro-inflammatory cytokine secretion from primary murine microglia and astrocytes, and human macrophages, stimulated with LPS, PIC, or Aß. CONCLUSIONS: ApoC-I is immunosuppressive. Our results illuminate a novel potential mechanism for APOE genotype risk for AD; one in which patients with an ε4 allele have decreased expression of apoC-I resulting in increased innate immune activity.
[Mh] Termos MeSH primário: Apolipoproteína C-I/metabolismo
Regulação da Expressão Gênica/genética
Neuroglia/metabolismo
[Mh] Termos MeSH secundário: Idoso
Peptídeos beta-Amiloides/farmacologia
Animais
Animais Recém-Nascidos
Apolipoproteína C-I/líquido cefalorraquidiano
Apolipoproteína C-I/genética
Apolipoproteína C-I/farmacologia
Apolipoproteína E3/genética
Apolipoproteína E4/genética
Astrócitos/efeitos de drogas
Astrócitos/metabolismo
Células Cultivadas
Córtex Cerebral/citologia
Citocinas/metabolismo
Ensaio de Imunoadsorção Enzimática
Feminino
Regulação da Expressão Gênica/efeitos de drogas
Genótipo
Proteína Glial Fibrilar Ácida/metabolismo
Humanos
Macrófagos/efeitos de drogas
Macrófagos/metabolismo
Camundongos
Camundongos Endogâmicos C57BL
Camundongos Transgênicos
Neuroglia/efeitos de drogas
Poli I-C/farmacologia
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, N.I.H., EXTRAMURAL
[Nm] Nome de substância:
0 (Amyloid beta-Peptides); 0 (Apolipoprotein C-I); 0 (Apolipoprotein E3); 0 (Apolipoprotein E4); 0 (Cytokines); 0 (Glial Fibrillary Acidic Protein); 24939-03-5 (Poly I-C)
[Em] Mês de entrada:1304
[Cu] Atualização por classe:130510
[Lr] Data última revisão:
130510
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:121107
[St] Status:MEDLINE
[do] DOI:10.1186/1742-2094-9-192



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