Search results for "Signaling"

showing 10 items of 1125 documents

TiFoSi: an efficient tool for mechanobiology simulations of epithelia

2020

[Motivation]: Emerging phenomena in developmental biology and tissue engineering are the result of feedbacks between gene expression and cell biomechanics. In that context, in silico experiments are a powerful tool to understand fundamental mechanisms and to formulate and test hypotheses.

Statistics and ProbabilityCell signalingCell divisionComputer scienceSystems biologyIn silicoCellBiophysicsMorphogenesisVertex ModelContext (language use)Computational biologyCleavage (embryo)BiochemistryEpitheliumFeedbackMechanobiologyEpithelia Simulation03 medical and health sciencesParacrine signallingMechanobiologyTissue engineeringMorphogenesismedicineComputer SimulationCellular dynamicsMolecular Biology030304 developmental biology0303 health sciencesSystems Biology030302 biochemistry & molecular biologyComputational BiologyCell cycleTissue SimulationJuxtacrine signallingComputer Science ApplicationsComputational Mathematicsmedicine.anatomical_structureComputational Theory and MathematicsDevelopmental biologyCell DivisionSoftwareDevelopmental BiologyBioinformatics
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Morphology changes induced by intercellular gap junction blocking: A reaction-diffusion mechanism.

2021

Complex anatomical form is regulated in part by endogenous physiological communication between cells; however, the dynamics by which gap junctional (GJ) states across tissues regulate morphology are still poorly understood. We employed a biophysical modeling approach combining different signaling molecules (morphogens) to qualitatively describe the anteroposterior and lateral morphology changes in model multicellular systems due to intercellular GJ blockade. The model is based on two assumptions for blocking-induced patterning: (i) the local concentrations of two small antagonistic morphogens diffusing through the GJs along the axial direction, together with that of an independent, uncouple…

Statistics and ProbabilityCell signalingModels BiologicalGeneral Biochemistry Genetics and Molecular BiologyDiffusionMorphogenesisAnimalsBlocking (linguistics)IonsNeurotransmitter AgentsbiologyMechanism (biology)ChemistryApplied MathematicsGap junctionGap JunctionsGeneral MedicinePlanariansbiology.organism_classificationPlanariaMulticellular organismIntercellular JunctionsModeling and SimulationBiophysicsReprogrammingAlgorithmsMorphogenSignal TransductionBio Systems
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Efficient differentiation of embryonic stem cells into mesodermal precursors by BMP, retinoic acid and Notch signalling

2012

The ability to direct differentiation of mouse embryonic stem (ES) cells into specific lineages not only provides new insights into the pathways that regulate lineage selection but also has translational applications, for example in drug discovery. We set out to develop a method of differentiating ES cells into mesodermal cells at high efficiency without first having to induce embryoid body formation. ES cells were plated on a feeder layer of PA6 cells, which have membrane-associated stromal-derived inducing activity (SDIA), the molecular basis of which is currently unknown. Stimulation of ES/PA6 co-cultures with Bone Morphogenetic Protein 4 (BMP4) both favoured self-renewal of ES cells and…

Stromal cellCellular differentiationMyocytes Smooth MuscleNotch signaling pathwaylcsh:MedicineDevelopmental SignalingTretinoinEmbryoid bodyBiologyCell LineMesoderm03 medical and health sciencesMice0302 clinical medicineRetinoic Acid Signaling CascadeMolecular Cell BiologyExpressió genèticaAnimalslcsh:ScienceBiologyEmbryonic Stem Cells030304 developmental biology0303 health sciencesMultidisciplinaryReceptors NotchStem Cellslcsh:RComputational BiologyCell DifferentiationNestinSignaling in Selected DisciplinesMolecular biologyEmbryonic stem cellSignaling CascadesSignaling NetworksP19 cellBone morphogenetic protein 4embryonic structuresBone Morphogenetic Proteinslcsh:QCellular TypesStromal CellsTranscriptomeCèl·lules mare030217 neurology & neurosurgeryResearch ArticleDevelopmental BiologySignal Transduction
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SYSCILIA, “A systems biology approach to dissect cilia function and its disruption in human genetic disease”

2012

Primary cilia are basically signaling hubs, harboring amongst others the noncanonical WNT, Hedgehog,and PDGF signaling systems, and their disruption leads to striking developmental defects. Some ciliopathy-associated proteins have recently been revealed to be physically or functionally associated in several distinct groupings, with limited connections to other crucial biological processes. Early proteomics studies have also suggested a discrete repertoire of about 1000 proteins within the organelle (i.e. <5% of the proteome) that are still in need of organisation into pathways and networks. Small, relatively isolated systems are often targeted by systems biology approaches under the assumpt…

Systems biologyCiliumProteomePoster PresentationWnt signaling pathwayCell BiologyComputational biologyBiologyProteomicsDevelopmental biologyHedgehogHuman geneticsCell biologyCilia
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Inhibition of Transcription Factors by Plant-Derived Compounds and their Implications in Inflammation and Cancer

2009

Inflammation is a general term used to describe various pathological processes with diverse causes that can include infection, trauma, or an autoimmune response. Due to its many causes, the inflammatory response involves multiple and varied mediators, including vasoactive amines, free radicals, and both lipidic and peptidic mediators. Medicinal plants and the compounds derived from them are a good source of new and specific inhibitors of the inflammatory process. The past decade has witnessed many important discoveries in this field, with new findings challenging the more traditional views of pharmacologists. Various studies, for example, have demonstrated the positive effects of plant-deri…

T-LymphocytesAnti-Inflammatory AgentsArthritisAntineoplastic AgentsInflammationPharmacologychemistry.chemical_compoundDrug DiscoverymedicineAnimalsHumansTranscription factorJanus KinasesPharmacologyNatural productbiologyNF-kappa BJAK-STAT signaling pathwayBiological activityPlantsmedicine.diseasechemistryBiochemistrybiology.proteinCyclooxygenaseSignal transductionmedicine.symptomSignal TransductionTranscription FactorsCurrent Pharmaceutical Design
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Diacylglycerol-containing oleic acid induces increases in [Ca(2+)](i) via TRPC3/6 channels in human T-cells.

2011

Though most of the studies have focused on the effects of free fatty acids on T-cell activation, fatty acids incorporated into plasma membrane phospholipids may also affect cell signaling via diacylglycerol (DAG), generally produced by phospholipid hydrolysis. In the present study, we have synthesized a DAG-containing oleic acid and studied its implication in the modulation of calcium signaling in human Jurkat T-cells. 1-palmitoyl-2-oleoyl-sn-glycerol (POG) induced a dose-dependent increase in [Ca(2+)](i). This effect was due to the presence of oleic acid at the sn-2 position as no differences were observed between POG and 1-stearoly-2-oleoyl-sn-glycerol (SOG). However, the substitution of …

T-LymphocytesPhospholipidGene ExpressionBiologyCaveolaeDiglycerideschemistry.chemical_compoundJurkat CellsTRPC3Membrane MicrodomainsTRPC6 Cation ChannelHumansCalcium SignalingMolecular BiologyLipid raftCalcium signalingDiacylglycerol kinaseTRPC Cation ChannelsIon TransportVoltage-dependent calcium channelDose-Response Relationship DrugReverse Transcriptase Polymerase Chain Reactionbeta-CyclodextrinsCell BiologyOleic acidchemistryBiochemistryMicroscopy Fluorescencelipids (amino acids peptides and proteins)Arachidonic acidCalciumRNA InterferenceBiochimica et biophysica acta
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A Regulatory Mechanism Involving TBP-1/Tat-Binding Protein 1 and Akt/PKB in the Control of Cell Proliferation

2011

Abstract TBP-1 /Tat-Binding Protein 1 (also named Rpt-5, S6a or PSMC3) is a multifunctional protein, originally identified as a regulator of HIV-1-Tat mediated transcription. It is an AAA-ATPase component of the 19S regulative subunit of the proteasome and, as other members of this protein family, fulfils different cellular functions including proteolysis and transcriptional regulation. We and others reported that over expression of TBP-1 diminishes cell proliferation in different cellular contexts with mechanisms yet to be defined. Accordingly, we demonstrated that TBP-1 binds to and stabilizes the p14ARF oncosuppressor increasing its anti-oncogenic functions. However, TBP-1 restrains cell…

TBP-1/Tat-Binding Protein 1lcsh:Medicinemacromolecular substancesBiologymTORC2Cell GrowthTBP-1/Tat-Binding Protein 1; cell proliferationp14arfMolecular Cell BiologyGeneticsCancer GeneticsTranscriptional regulationGene Networkslcsh:ScienceBiologyProtein kinase BPI3K/AKT/mTOR pathwayMultidisciplinaryCell growthAKTBinding proteinlcsh:RMolecular biologySignaling CascadesCell biologyTBP-1enzymes and coenzymes (carbohydrates)cell proliferationbiology.proteinMdm2lcsh:QCell DivisionResearch ArticleSignal TransductionPLoS ONE
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The Activation Status of the TGF-β Transducer Smad2 Is Associated with a Reduced Survival in Gastrointestinal Cancers: A Systematic Review and Meta-A…

2019

Aberrant function of Smad2, a crucial member of transforming growth factor beta (TGF-β) signaling, is associated with the development of malignancies, particularly in the gastrointestinal district. However, little is known about its possible prognostic role in such tumor types. With the first meta-analysis on this topic, we demonstrated that the lack of the activated form of Smad2 (phosphor-Smad2 or pSmad2), which was meant to be the C-terminally phosphorylated form, showed a statistically significant association with an increased risk of all-cause mortality in patients with gastrointestinal cancers (RR, 1.58; 95% CI, 1.05–2.37, p = 0.029, I2 = 84%), also after having adjusted for potential…

TGF-β0301 basic medicineOncologymedicine.medical_specialtySmad2 ProteinReviewCatalysislcsh:ChemistryInorganic Chemistry03 medical and health sciences0302 clinical medicineTransforming Growth Factor betaInternal medicineOdds RatiomedicineHumansIn patientPhysical and Theoretical Chemistrylcsh:QH301-705.5Molecular BiologySpectroscopyGastrointestinal Neoplasmsbiologyphosphorylationbusiness.industryOrganic ChemistryConfoundingCancerGeneral MedicineTransforming growth factor betaPrognosismedicine.diseaseComputer Science Applications030104 developmental biologyIncreased risklcsh:Biology (General)lcsh:QD1-999pSmad2030220 oncology & carcinogenesisMeta-analysisbiology.proteinPhosphorylationsignalingbusinessPublication BiasBiomarkersSmad2Signal TransductionTransforming growth factorInternational Journal of Molecular Sciences
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Strategies to Target ADAM17 in Disease: From Its Discovery to the iRhom Revolution

2021

For decades, disintegrin and metalloproteinase 17 (ADAM17) has been the object of deep investigation. Since its discovery as the tumor necrosis factor convertase, it has been considered a major drug target, especially in the context of inflammatory diseases and cancer. Nevertheless, the development of drugs targeting ADAM17 has been harder than expected. This has generally been due to its multifunctionality, with over 80 different transmembrane proteins other than tumor necrosis factor α (TNF) being released by ADAM17, and its structural similarity to other metalloproteinases. This review provides an overview of the different roles of ADAM17 in disease and the effects of its ablation in a n…

TIMPsEGFRiRhomsTNFAnti-Inflammatory AgentsPharmaceutical ScienceInflammationContext (language use)Antineoplastic AgentsDiseaseComputational biologyReviewADAM17 ProteinmetalloproteinasesAnalytical Chemistrylcsh:QD241-44103 medical and health sciences0302 clinical medicineImmune systemlcsh:Organic chemistryIn vivoNeoplasmsDrug DiscoverymedicineDisintegrinTIMPADAM17 ProteinAnimalsHumansPhysical and Theoretical Chemistry030304 developmental biologyInflammation0303 health sciencesADAM17biologyOrganic ChemistryIntracellular Signaling Peptides and ProteinsiRhomChemistry (miscellaneous)030220 oncology & carcinogenesisbiology.proteinADAM17; Ectodomain shedding; EGFR; IRhoms; Metalloproteinases; TIMPs; TNF; ADAM17 Protein; Animals; Anti-Inflammatory Agents; Antineoplastic Agents; Humans; Inflammation; Intracellular Signaling Peptides and Proteins; NeoplasmsMolecular MedicineTumor necrosis factor alphametalloproteinaseectodomain sheddingmedicine.symptomMolecules
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Hematopoietic stem cell quiescence and function are controlled by the CYLD–TRAF2–p38MAPK pathway

2015

Tesio at al. identify a novel pathway controlled by the tumor suppressor and deubiquitinase cylindromatosis (CYLD), which is involved in the regulation of hematopoietic stem cell quiescence and repopulation potential.

TRAF2Tumor suppressor geneMAP Kinase Signaling SystemImmunologyRegulatorBiologyp38 Mitogen-Activated Protein KinasesArticleMicemedicineAnimalsImmunology and AllergyMice KnockoutRegulation of gene expressionNF-kappa BHematopoietic stem cellCell BiologyHematopoietic Stem CellsTNF Receptor-Associated Factor 2PhenotypeDeubiquitinating Enzyme CYLDCell biologyCysteine EndopeptidasesHaematopoiesismedicine.anatomical_structureGene Expression RegulationMutationStem cellJournal of Experimental Medicine
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