Search results for "Gene Expression"

showing 10 items of 4085 documents

Dual roles of Aβ in proliferative processes in an amyloidogenic model of Alzheimer’s disease

2017

Alzheimer’s disease is a major neurodegenerative disorder that leads to severe cognitive deficits in the elderly population. Over the past two decades, multiple studies have focused on elucidating the causative factors underlying memory defects in Alzheimer’s patients. In this regard, new evidence linking Alzheimer’s disease-related pathology and neuronal stem cells suggests that hippocampal neurogenesis impairment is an important factor underlying these cognitive deficits. However, because of conflicting results, the impact of Aβ pathology on neurogenesis/gliogenesis remains unclear. Here, we investigated the effect of Aβ on neuronal and glial proliferation by using an APP/PS1 transgenic m…

Doublecortin Domain ProteinsMale0301 basic medicineCellular pathologyPathologymedicine.medical_specialtyNeurogenesisGene ExpressionHippocampuslcsh:MedicineMice TransgenicBiologyHippocampusArticleAmyloid beta-Protein PrecursorMice03 medical and health sciences0302 clinical medicineNeural Stem CellsAlzheimer DiseaseSpheroids CellularNeurospheremedicineAnimalsHumansProgenitor celllcsh:ScienceCells CulturedCell ProliferationGliogenesisNeuronsAmyloid beta-PeptidesMultidisciplinaryNeuropeptidesNeurogenesislcsh:RCell DifferentiationNeural stem cellDisease Models Animal030104 developmental biologynervous systemOrgan Specificitylcsh:QStem cellMicrotubule-Associated ProteinsNeurogliaNeuroscience030217 neurology & neurosurgery
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Chronic fluoxetine treatment in middle-aged rats induces changes in the expression of plasticity-related molecules and in neurogenesis

2012

Abstract Background Antidepressants promote neuronal structural plasticity in young-adult rodents, but little is known of their effects on older animals. The polysialylated form of the neural cell adhesion molecule (PSA-NCAM) may mediate these structural changes through its anti-adhesive properties. PSA-NCAM is expressed in immature neurons and in a subpopulation of mature interneurons and its expression is modulated by antidepressants in the telencephalon of young-adult rodents. Results We have analyzed the effects of 14 days of fluoxetine treatment on the density of puncta expressing PSA-NCAM and different presynaptic markers in the medial prefrontal cortex, hippocampus and amygdala of mi…

Doublecortin Domain ProteinsMaleTelencephalonmedicine.medical_specialtyDoublecortin ProteinVesicular glutamate transporter 1NeurogenesisGlutamate decarboxylaseSynaptophysinHippocampusSubventricular zoneCell CountNeural Cell Adhesion Molecule L1Hippocampal formationSubgranular zonelcsh:RC321-571Cellular and Molecular NeuroscienceInternal medicineFluoxetineLateral VentriclesmedicineAnimalsRats Wistarlcsh:Neurosciences. Biological psychiatry. NeuropsychiatryCell ProliferationbiologyGlutamate DecarboxylaseGeneral NeuroscienceNeurogenesisBody WeightNeuropeptideslcsh:QP351-495DoublecortinRatsEndocrinologymedicine.anatomical_structureKi-67 Antigenlcsh:Neurophysiology and neuropsychologyGene Expression Regulationnervous systemVesicular Glutamate Transport Protein 1biology.proteinSialic AcidsAntidepressive Agents Second-GenerationNeuroscienceMicrotubule-Associated ProteinsResearch ArticleBMC Neuroscience
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Chronic non-invasive glucocorticoid administration decreases polysialylated neural cell adhesion molecule expression in the adult rat dentate gyrus

2004

The expression of the polysialylated neural cell adhesion molecule (PSA-NCAM) is increased in the hippocampus after chronic restraint stress (CRS) and may play a permissive role in structural changes that include dendrite reorganization in dentate gyrus (DG) and CA3 pyramidal neurons and suppression of neurogenesis in DG. We report that chronic oral corticosterone (CORT) administration decreases the number of PSA-NCAM immunoreactive granule neurons in the adult rat dentate gyrus, and the available evidence suggests that this is an indirect effect of CORT, possibly involving excitatory amino acids, that may not be directly related to neurogenesis. Because CORT treatment reduces but does not …

Doublecortin Domain ProteinsMalemedicine.medical_specialtyCentral nervous systemAdministration OralCell CountNeural Cell Adhesion Molecule L1BiologyRats Sprague-Dawleychemistry.chemical_compoundCorticosteroneInternal medicinemedicineAnimalsPermissiveGlucocorticoidsNeuronsCell growthGeneral NeuroscienceDentate gyrusNeuropeptidesNeurogenesisImmunohistochemistryRatsKi-67 AntigenEndocrinologymedicine.anatomical_structureGene Expression Regulationnervous systemchemistryDentate GyrusSialic AcidsNeural cell adhesion moleculeMicrotubule-Associated ProteinsGlucocorticoidmedicine.drugNeuroscience Letters
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Divergent impact of the polysialyltransferases ST8SiaII and ST8SiaIV on polysialic acid expression in immature neurons and interneurons of the adult …

2010

Polysialic acid (PSA) is a negatively charged carbohydrate polymer, which confers antiadhesive properties to the neural cell adhesion molecule NCAM and facilitates cellular plasticity during brain development. In mice, PSA expression decreases drastically during the first postnatal weeks and it gets confined to immature neurons and regions displaying structural plasticity during adulthood. In the brain, PSA is exclusively synthesized by the two polysialyltransferases ST8SiaII and ST8SiaIV. To study their individual contribution to polysialylation in the adult, we analyzed PSA expression in mice deficient for either polysialyltransferase. Focusing on the cerebral cortex, our results indicate…

Doublecortin Domain ProteinsNeurogenesisHippocampal formationHippocampusSubgranular zoneMiceInterneuronsmedicineNeuropilAnimalsCerebral CortexMice KnockoutNeuronsNeuronal PlasticitybiologyPolysialic acidGeneral NeuroscienceStem CellsNeurogenesisNeuropeptidesGene Expression Regulation DevelopmentalCell DifferentiationCD56 AntigenSialyltransferasesDoublecortinCell biologyMice Inbred C57BLmedicine.anatomical_structurenervous systemCerebral cortexbiology.proteinSialic AcidsNeural cell adhesion moleculeNeuroscienceMicrotubule-Associated ProteinsNeuroscience
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Sox2-Mediated Conversion of NG2 Glia into Induced Neurons in the Injured Adult Cerebral Cortex

2014

Summary The adult cerebral cortex lacks the capacity to replace degenerated neurons following traumatic injury. Conversion of nonneuronal cells into induced neurons has been proposed as an innovative strategy toward brain repair. Here, we show that retrovirus-mediated expression of the transcription factors Sox2 and Ascl1, but strikingly also Sox2 alone, can induce the conversion of genetically fate-mapped NG2 glia into induced doublecortin (DCX)+ neurons in the adult mouse cerebral cortex following stab wound injury in vivo. In contrast, lentiviral expression of Sox2 in the unlesioned cortex failed to convert oligodendroglial and astroglial cells into DCX+ cells. Neurons induced following …

Doublecortin ProteinGene ExpressionBiochemistryArticleMiceSOX2Cortex (anatomy)Basic Helix-Loop-Helix Transcription FactorsGeneticsmedicineAnimalslcsh:QH301-705.5Cell ProliferationCerebral CortexNeuronslcsh:R5-920biologySOXB1 Transcription FactorsCell BiologyAnatomySynaptic PotentialsCellular ReprogrammingDoublecortinASCL1medicine.anatomical_structurelcsh:Biology (General)nervous systemCerebral cortexCell Transdifferentiationbiology.proteinNeurogliaNeuNlcsh:Medicine (General)NeurogliaReprogrammingNeuroscienceDevelopmental BiologyStem Cell Reports
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Functional Integration of Neuronal Precursors in the Adult Murine Piriform Cortex

2018

Abstract The extent of functional maturation and integration of nonproliferative neuronal precursors, becoming neurons in the adult murine piriform cortex, is largely unexplored. We thus questioned whether precursors eventually become equivalent to neighboring principal neurons or whether they represent a novel functional network element. Adult brain neuronal precursors and immature neurons (complex cells) were labeled in transgenic mice (DCX-DsRed and DCX-CreERT2 /flox-EGFP), and their cell fate was characterized with patch clamp experiments and morphometric analysis of axon initial segments. Young (DCX+) complex cells in the piriform cortex of 2- to 4-month-old mice received sparse synapt…

Doublecortin ProteinNeurogenesisCognitive NeuroscienceMice TransgenicPiriform CortexBiologyCell fate determinationtangled cellsaxon initial segmentMiceCellular and Molecular NeuroscienceNeural Stem CellsdoublecortinPiriform cortexmedicineAnimalsPatch clampNeuronsNeuropeptidesNeurogenesisGene Expression Regulation DevelopmentalCell Differentiationcomplex cellsAxon initial segmentDoublecortinadult neurogenesismedicine.anatomical_structurenervous systembiology.proteinGABAergicOriginal ArticleNeuronMicrotubule-Associated ProteinsNeuroscienceCerebral Cortex
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Identification of proteins and developmental expression of RNAs encoded by the 65A cuticle protein gene cluster in Drosophila melanogaster

1998

0965-1748 (Print) Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.; Proteins of the third instar larval cuticle of Drosophila melanogaster, LCP5-LCP9, were purified and their N-terminal sequences determined. Three of these proteins (LCP5, 6, and 8) were found to be encoded by two multicopy genes previously mapped to the gene cluster at 65A 5-6 on the left arm of the third chromosome. The analysis of the patterns of developmental expression of the 8 distinct genes at this site showed that all but two were expressed during larval life. The patterns fell into three groups: one where expression was all through larval life, one where expression was primar…

Drosophila melanogaster/*genetics/growth & developmentCuticleMolecular Sequence DataInsect Proteins/*genetics/isolation & purificationSequence HomologyGenes InsectLarva/genetics/growth & developmentBiochemistryGene clusterAnimalsDevelopmentalAmino Acid SequenceMolecular BiologyGeneGeneticsRegulation of gene expressionSequence Homology Amino AcidbiologyfungiGene Expression Regulation DevelopmentalChromosome Mappingbiology.organism_classificationAmino AcidDrosophila melanogasterGene Expression RegulationGenesLarvaMultigene FamilyInsect ScienceEcdysisRNA/*geneticsInsect ProteinsRNAInstarDrosophila melanogasterInsectOverlapping geneInsect Biochemistry and Molecular Biology
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Interspecific transgenic analysis of basal versus heat-shock-induced expression of a Drosophila pseudoobscura hsp82-neo fusion gene in D. melanogaster

1994

Drosophila melanogaster transformants containing a D. pseudoobscura hsp82-neo fusion gene were used to examine the relationship between chromosome structure and its variation to transcriptional activation and gene expression. At normal temperatures (25° C) transgenic hsp82-neo was transcribed in diffuse polytene chromosomal bands encoding antibiotic G418-resistance without intensive puff formation. Substantial basal expression of the transgene was observed in all tissues examined: salivary glands, brain, ventral ganglion, foregut, gastric caeca, midgut, imaginal discs, nurse cells and oocytes. In addition, basal hsp82-neo expression occurred throughout embryogenesis. In third-instar larvae …

Drosophila pseudoobscuraPolytene chromosomebiologyTransgeneGene expressionGeneticsMelanogasterIntronEctopic expressionDrosophila melanogasterbiology.organism_classificationMolecular biologyDevelopmental BiologyRoux's Archives of Developmental Biology
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Heterogeneity in the Response of Different Subtypes of Drosophila melanogaster Midgut Cells to Viral Infections

2021

This article belongs to the Section Viral Immunology, Vaccines, and Antivirals.

Drosophila virusesSingle-cell genomicsvirusesVirus-host interactionMicrobiologyViruscell-type-specific gene expressionTranscriptomeVirologyMelanogasterHeat shockGeneSingle-cell RNA-seqsingle-cell RNA-seqvirus-host interactionbiologydual RNA-seqsingle-cell genomicsRNAbiology.organism_classificationVirologyQR1-502Infectious DiseasesViral replicationantiviral heat shock responseCell-type-specific gene expression<i>Drosophila</i> virusesDrosophila melanogasterDual RNA-seqViruses
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Topoisomerase II{alpha}-dependent and -independent apoptotic effects of dexrazoxane and doxorubicin.

2009

Abstract Coadministration of the iron chelator dexrazoxane reduces by 80% the incidence of heart failure in cancer patients treated with anthracyclines. The clinical application of dexrazoxane is limited, however, because its ability to inhibit topoisomerase IIα (TOP2A) is feared to adversely affect anthracycline chemotherapy, which involves TOP2A-mediated generation of DNA double-strand breaks (DSB). Here, we investigated the apoptotic effects of dexrazoxane and the anthracycline doxorubicin, alone and in combination, in a tumor cell line with conditionally regulated expression of TOP2A. Each drug caused apoptosis that was only partly dependent on TOP2A. Unexpectedly, dexrazoxane was found…

DrugCancer ResearchAnthracyclinemedicine.medical_treatmentmedia_common.quotation_subjectAntineoplastic AgentsApoptosisPharmacologyHistonesAntigens NeoplasmCell Line TumormedicineHumansDoxorubicinAdverse effectPoly-ADP-Ribose Binding Proteinsmedia_commonCaspase 7ChemotherapyChemistryCaspase 3Gene Expression ProfilingCancermedicine.diseaseGlutathioneDNA-Binding ProteinsGene Expression Regulation NeoplasticDNA Topoisomerases Type IIOncologyApoptosisDoxorubicinCancer researchDexrazoxaneTumor Suppressor Protein p53Razoxanemedicine.drugMolecular cancer therapeutics
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