Search results for "Myocyte"

showing 10 items of 248 documents

Morphology of Skeletal Muscle

2013

Skeletal muscle makes up the largest organ of the body, by both volume and weight, comprising more than 40 %. More than 500 diseases concern muscle tissue, the majority of which originate in muscle, others secondarily affect the muscle, foremost by denervation. The functional and structural dependence of skeletal muscle on innervation—that is, the peripheral and central nervous systems—renders muscle tissue unique and adds a dimension to the nosology, more obviously than in other organs. Therefore, diseases affecting muscle are also termed neuromuscular diseases. Within the nosological spectrum of the muscle parenchyma, which encompasses hereditary and acquired conditions, muscular dystroph…

DenervationMuscle tissuePathologymedicine.medical_specialtybusiness.industrySkeletal musclePeriodic paralysismedicine.diseaseExtraocular musclesmedicine.anatomical_structureEndocrine pathologymedicineMyocyteMuscular dystrophybusiness
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Overexpression of the truncated form of high mobility group a proteins (HMGA2) in human myometrial cells induces leiomyoma-like tissue formation

2014

The pathogenesis of uterine leiomyomas, the most common benign tumor in women, is still unknown. This lack of basic knowledge limits the development of novel non-invasive therapies. Our group has previously demonstrated that leiomyoma side population (SP) cells are present in tumor lesions and act like putative tumor-initiating stemcells in human leiomyoma. Moreover, accumulated evidence demonstrates that these benign tumors of mesenchymal origin are characterized by rearrangements of the High Mobility Group A proteins (HMGA). In this work, we tested the hypothesis that leiomyoma development may be due to overexpression of HMGA2 (encoding high mobility group AT-hook2) in myometrial stem cel…

EmbryologyMice SCID//purl.org/becyt/ford/1 [https]MiceMice Inbred NODProtein IsoformsUterine leiomyomaLeiomyomaStem CellsSOMATIC STEM CELLSObstetrics and GynecologyExonsBioquímica y Biología Molecularfemale genital diseases and pregnancy complicationsGene Expression Regulation NeoplasticCell Transformation NeoplasticLeiomyomaUterine NeoplasmsMyometriumNeoplastic Stem CellsFemaleStem cellHIGH MOBILITY GROUP A PROTEINSCIENCIAS NATURALES Y EXACTASPlasmidsAdult stem cellmedicine.medical_specialtyUTERINE LEIOMYOMASMyocytes Smooth MuscleTransplantation HeterologousBiologyTransfectionHUMAN MYOMETRIUMCiencias BiológicasHMGA2Side populationInternal medicineGeneticsmedicineAnimalsHumans//purl.org/becyt/ford/1.6 [https]neoplasmsMolecular BiologyHMGA2 ProteinMesenchymal stem cellHMGASIDE POPULATIONCell Biologymedicine.diseaseIntronsEndocrinologyReproductive MedicineCancer researchbiology.proteinDevelopmental Biology
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Three-dimensional cardiac computational modelling: methods, features and applications

2015

[EN] The combination of computational models and biophysical simulations can help to interpret an array of experimental data and contribute to the understanding, diagnosis and treatment of complex diseases such as cardiac arrhythmias. For this reason, three-dimensional (3D) cardiac computational modelling is currently a rising field of research. The advance of medical imaging technology over the last decades has allowed the evolution from generic to patient-specific 3D cardiac models that faithfully represent the anatomy and different cardiac features of a given alive subject. Here we analyse sixty representative 3D cardiac computational models developed and published during the last fifty …

Engineeringmedicine.medical_treatmentFibre orientationReviewCardiac conduction system (CCS)computer.software_genreField (computer science)Cardiac Resynchronization TherapyCardiac modellingImage Processing Computer-AssistedMyocytes CardiacPrecision MedicineBiophysical simulationDecision Making Computer-AssistedBiological dataComputational modelRadiological and Ultrasound TechnologyCardiac electrophysiologyModels CardiovascularBiophysical PhenomenaGeneral MedicineBiomechanical PhenomenaElectrophysiologyRabbitsThree-dimensional (3D) modellingHeart DiseasesPersonalisationPatient-specific modellingCardiologyCardiac resynchronization therapyBiomedical EngineeringMachine learningBiophysical PhenomenaTECNOLOGIA ELECTRONICABiomaterialsDogsHeart Conduction SystemmedicineAnimalsHumansComputer SimulationRadiology Nuclear Medicine and imagingbusiness.industryMyocardiumExperimental dataImage segmentationCardiac image segmentationComputational modellingArtificial intelligencebusinesscomputerBioMedical Engineering OnLine
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Arsenic trioxide alters the differentiation of mouse embryonic stem cell into cardiomyocytes

2015

AbstractChronic arsenic exposure is associated with increased morbidity and mortality for cardiovascular diseases. Arsenic increases myocardial infarction mortality in young adulthood, suggesting that exposure during foetal life correlates with cardiac alterations emerging later. Here, we investigated the mechanisms of arsenic trioxide (ATO) cardiomyocytes disruption during their differentiation from mouse embryonic stem cells. Throughout 15 days of differentiation in the presence of ATO (0.1, 0.5, 1.0 μM) we analysed: the expression of i) marker genes of mesoderm (day 4), myofibrillogenic commitment (day 7) and post-natal-like cardiomyocytes (day 15); ii) sarcomeric proteins and their orga…

Fetal ProteinsSarcomeresMesodermTime FactorsCellular differentiationBlotting WesternConnexinFluorescent Antibody TechniqueGene ExpressionAntineoplastic AgentsActininBiologyArticleArsenicalsCell Linechemistry.chemical_compoundMiceArsenic TrioxideTroponin TSpheroids CellularGene expressionmedicineAnimalsActininMyocytes CardiacArsenic trioxideHomeodomain ProteinsSyncytiumMultidisciplinaryReverse Transcriptase Polymerase Chain ReactionCell DifferentiationMouse Embryonic Stem CellsOxidesEmbryonic stem cellCell biologyBiomechanical PhenomenaGATA4 Transcription Factormedicine.anatomical_structurechemistryConnexin 43ImmunologyHomeobox Protein Nkx-2.5T-Box Domain ProteinsTroponin CTranscription FactorsScientific Reports
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Cardiac arrhythmias induced by an electrical stimulation at a cellular level

2008

To provide insights into the impulse propagation between cardiac myocytes, we performed studies of excitation spread with cellular resolution in confluent monolayers of cultured cardiomyocytes (CM). Multisite field potentials have been recorded using microelectrode arrays (MEA) technology in a basal condition and in proarrhythmic conditions induced by a high frequency electrical stimulation. The in vitro observation of spiral waves opens a new way to test the anti-arrhythmic drugs or strategies at cellular level.

Fibrillation0303 health sciencesmedicine.medical_specialtyChemistry[SDV]Life Sciences [q-bio]Stimulation030204 cardiovascular system & hematologyCellular level[SPI]Engineering Sciences [physics]03 medical and health sciencesMicroelectrode0302 clinical medicineCellular resolutionInternal medicinemedicineBiophysicsCardiologyMyocyte[NLIN]Nonlinear Sciences [physics]medicine.symptomComputingMilieux_MISCELLANEOUS030304 developmental biology2008 Computers in Cardiology
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Nitric oxide synthase isozymes antibodies

1995

Three isozymes of nitric oxide synthase (NOS) have been identified, cDNAs isolated and sequenced, and antibodies produced against each isozyme. Isozyme I (found primarily in central and peripheral neuronal cells), II (in cytokine-induced cells), and III (in endothelial cells) show less than 58% identity in the deduced amino acid sequences from humans. Many investigators have produced isozyme-specific antibodies and used these antibodies to locate these proteins in various cells and tissues. NOS-I is constitutively expressed, and the enzymatic activity is regulated by Ca2+ and calmodulin. The anti-NOS-I antibodies have allowed investigators to characterize non-adrenergic non-cholinergic neur…

Gene isoformmedicine.medical_specialtyCell typeCalmodulinPancreatic isletsInflammationCell BiologyBiologyIsozymeMolecular biologyNitric oxide synthaseEndocrinologymedicine.anatomical_structureInternal medicinebiology.proteinmedicineMyocyteAnatomymedicine.symptomThe Histochemical Journal
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Sciences within European Young Researcher Community272The neuro-cardiac interaction defines an extracellular microdomain required for neurotrophic si…

2016

# 272 The neuro-cardiac interaction defines an extracellular microdomain required for neurotrophic signaling {#article-title-2} Purpose: Sympathetic neurons (SNs) innervate the myocardium with a defined topology that allows physiological modulation of cardiac activity. Limiting amounts of neurotrophins released by cardiac cells control SN viability and myocardial distribution, whose impairment has been described in a number of heart diseases (e.g. myocardial infarction, heart failure). Therefore, the fine control of cardiac innervation is crucial to ensure the physiological sympathetic function. It has been demonstrated that SNs directly interact with cardiomyocytes (CMs). Although it has b…

Genetically modified mousemedicine.medical_specialtybiologyTyrosine hydroxylasePhysiologyPhysiologyTropomyosin receptor kinase AAngiotensin IIEndocrinologymedicine.anatomical_structurePhysiology (medical)Internal medicinebiology.proteinmedicineMyocyteNeuronCardiology and Cardiovascular MedicineHomeostasisNeurotrophinCardiovascular Research
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Gesteigerte Expression des Tunnelproteins Connexin43 in der obstruierten Rattenblase - eine mögliche Ursache obstruktionsbedingter Blasenhyperaktivit…

2002

Fragestellung: Blasenhyperaktivitat ist ein haufiges und belastendes Symptom der Blasenauslassobstruktion und persistiert oft auch nach effektiver Deobstruierung. Gap junctions werden schon langer als mogliche Ursache von Blasenhyperaktivitat diskutiert. Wir untersuchten die regionale Verteilung des Gap-junction-Proteins Connexin43 in obstruierten und nicht obstruierten Rattenblasen. Material und Methode: Durch partielle Ligatur der Urethra wurde eine Obstruktion bei weiblichen Ratten erzeugt. Nach 6 Wochen wurden die Blasen entnommen und fur den molekularbiologischen Nachweis von Connexin43-mRNS durch kompetitive RT-PCR oder die immunhistochemische Detektion von Connexin43-Protein weiterve…

Gynecologymedicine.medical_specialtybusiness.industryUrologymedicine.medical_treatmentGap junctionAnatomyurologic and male genital diseasesBladder instabilityBladder outlet obstructionUrethramedicine.anatomical_structureSmooth musclecardiovascular systemmedicineMyocytebusinessLigatureInput resistanceAktuelle Urologie
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Biomarkers in heart failure

2009

Nowadays, heart failure (HF) has an increasing prevalence, particularly in the elderly, and is becoming a clinical problem of epidemic proportion in terms of morbidity and mortality. Developing biological markers, that can aid in the diagnosis of HF and in the differentiation of congestive heart failure (CHF) from other causes of dyspnoea, will reduce the cost of health care. However, an ideal biomarker has not yet been identified. Potential markers of HF include neuro-hormonal mediators, markers of myocyte injury, and indicators of systemic inflammation. Among these, the BNP and NT-pro-BNP are the most widely studied and appear to be useful in patients with dyspnoea of unknown aetiology, a…

Heart Failuremedicine.medical_specialtybusiness.industryUnknown aetiologymedicine.diseaseSystemic inflammationHeart failureHealth caremedicineBiomarker (medicine)HumansIn patientMyocyte injurymedicine.symptomBiomarkers heart failurebusinessIntensive care medicineRisk assessmentBiomarkers
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Impaired Binding to Junctophilin-2 and Nanostructural Alteration in CPVT Mutation

2021

Rationale: Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a rare disease, manifested by syncope or sudden death in children or young adults under stress conditions. Mutations in the Ca 2+ release channel/RyR2 (type 2 ryanodine receptor) gene account for about 60% of the identified mutations. Recently, we found and described a mutation in RyR2 N-terminal domain, RyR2 R420Q . Objective: To determine the arrhythmogenic mechanisms of this mutation. Methods and Results: Ventricular tachycardias under stress conditions were observed in both patients with catecholaminergic polymorphic ventricular tachycardia and knock-in mice. During action potential recording (by patch-clamp in …

Ile de francePhysiologyCPVT030204 cardiovascular system & hematologyArticle03 medical and health sciences0302 clinical medicineaction potential[SDV.MHEP.CSC]Life Sciences [q-bio]/Human health and pathology/Cardiology and cardiovascular systemPolitical sciencejunctophilinryanodine receptormedia_common.cataloged_instanceHumansEuropean union610 Medicine & health030304 developmental biologymedia_common0303 health sciencescalciumRyanodine Receptor Calcium Release ChannelRyR2musculoskeletal systemSarcoplasmic ReticulumDeath Sudden Cardiaccalcium induced calcium releaseGain of Function Mutationcardiomyocyte calcium handlingcardiovascular systemventricular tachycardiamutationCardiology and Cardiovascular MedicineHumanities
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