Search results for "Linea"

showing 10 items of 7724 documents

In vivo reprogramming for tissue repair.

2015

Berninger and colleagues define milestones for in vivo reprogramming and discuss recent developments in reprogramming into pancreatic b-cells and neurons. Vital organs such as the pancreas and the brain lack the capacity for effective regeneration. To overcome this limitation, an emerging strategy consists of converting resident tissue-specific cells into the cell types that are lost due to disease by a process called in vivo lineage reprogramming. Here we discuss recent breakthroughs in regenerating pancreatic β-cells and neurons from various cell types, and highlight fundamental challenges that need to be overcome for the translation of in vivo lineage reprogramming into therapy.

Cell typeLineage (genetic)Cell- and Tissue-Based TherapyAcinar CellsBiologyIn vivoInsulin-Secreting CellsmedicineHumansRegenerationCell LineagePancreasNeuronsBrain DiseasesRegeneration (biology)BrainPancreatic DiseasesTranslation (biology)Cell DifferentiationCell BiologyTissue repairCellular ReprogrammingCell biologymedicine.anatomical_structurePancreasReprogrammingNeurogliaNature cell biology
researchProduct

Expression and Function of Class II I-Ak Antigens on an Antigen-Specific T-Suppressor Cell Clone

1986

The question of whether similar or different modes of Ia-antigen expression exist in different cell classes and mediate different cell type functions is of primary interest to current class II antigen research. Among cells of the lymphoid system in the mouse, class II antigens are primarily expressed on B lymphocytes (Sachs and Cone 1973) and cells of the macrophage lineage (Cowing et al. 1978), whereas the majority of T lymphocytes do not seem to express endogenously synthesized class II antigens.

Cell typeLineage (genetic)Lymphatic systemmedicine.anatomical_structureAntigenCellmedicineMacrophageBiologyClone (B-cell biology)Molecular biologyPan-T antigens
researchProduct

Lineage-reprogramming of Pericyte-derived Cells of the Adult Human Brain into Induced Neurons

2014

Direct lineage-reprogramming of non-neuronal cells into induced neurons (iNs) may provide insights into the molecular mechanisms underlying neurogenesis and enable new strategies for in vitro modeling or repairing the diseased brain. Identifying brain-resident non-neuronal cell types amenable to direct conversion into iNs might allow for launching such an approach in situ, i.e. within the damaged brain tissue. Here we describe a protocol developed in the attempt of identifying cells derived from the adult human brain that fulfill this premise. This protocol involves: (1) the culturing of human cells from the cerebral cortex obtained from adult human brain biopsies; (2) the in vitro expansio…

Cell typePatch-Clamp TechniquesGeneral Chemical EngineeringCell Culture TechniquesBiologyGeneral Biochemistry Genetics and Molecular BiologySOX2Transduction GeneticmedicineHumansCell LineageCerebral CortexNeuronsGeneral Immunology and MicrobiologyGeneral NeuroscienceSOXB1 Transcription FactorsNeurogenesisHuman brainCell sortingCellular ReprogrammingFlow CytometryImmunohistochemistrymedicine.anatomical_structureRetroviridaeCell culturePericytePericytesNeuroscienceReprogrammingNeuroscience
researchProduct

Timing of identity: spatiotemporal regulation of hunchback in neuroblast lineages of Drosophila by Seven-up and Prospero.

2006

Neural stem cells often generate different cell types in a fixed birth order as a result of temporal specification of the progenitors. In Drosophila, the first temporal identity of most neural stem cells(neuroblasts) in the embryonic ventral nerve cord is specified by the transient expression of the transcription factor Hunchback. When reaching the next temporal identity, this expression is switched off in the neuroblasts by seven up (svp) in a mitosis-dependent manner, but is maintained in their progeny (ganglion mother cells). We show that svpmRNA is already expressed in the neuroblasts before this division. After mitosis, Svp protein accumulates in both cells, but the downregulation of h…

Cell typeReceptors Steroidanimal structuresTranscription GeneticMitosisNerve Tissue ProteinsNeuroblastAnimalsDrosophila ProteinsCell LineageProgenitor cellMolecular BiologyMitosisGeneticsNeuronsbiologyStem CellsfungiGene Expression Regulation DevelopmentalNuclear ProteinsProsperobiology.organism_classificationEmbryonic stem cellNeural stem cellCell biologyDNA-Binding ProteinsDrosophila melanogasterGanglion mother cellDevelopmental BiologyTranscription FactorsDevelopment (Cambridge, England)
researchProduct

Modeling Local Social Migrations: A Cellular Automata Approach

2015

In local social migrations, agents move from their initial location looking for a better local social environment. Social migrations processes do not change the number of social agents of a given type (i.e., the empirical distribution of the population) but their spatial location. Although cellular automata seems to appear as a natural approach to model of social migrations, the evolution of the configuration through a cellular automata might induce a new configuration wherein the number of agents of each type might be actually modified. This article provides a characterization of these cellular automata rules such that for any initial empirical distribution, the evolution of the configurat…

Cellular automataClass (set theory)education.field_of_studyTheoretical computer scienceProperty (philosophy)PopulationSocial environmentType (model theory)Nonlinear Sciences::Cellular Automata and Lattice GasesEmpirical distribution functionCellular automatonArtificial IntelligenceORGANIZACION DE EMPRESASNatural approacheducationAlgorithmSoftwareSocial migrationsInformation SystemsMathematics
researchProduct

The ladybird homeobox genes are essential for the specification of a subpopulation of neural cells

2004

AbstractIn Drosophila, neurons and glial cells are produced by neural precursor cells called neuroblasts (NBs), which can be individually identified. Each NB generates a characteristic cell lineage specified by a precise spatiotemporal control of gene expression within the NB and its progeny. Here we show that the homeobox genes ladybird early and ladybird late are expressed in subsets of cells deriving from neuroblasts NB 5-3 and NB 5-6 and are essential for their correct development. Our analysis revealed that ladybird in Drosophila, like their vertebrate orthologous Lbx1 genes, play an important role in cell fate specification processes. Among those cells that express ladybird are NB 5-6…

Cellular differentiationApoptosisAnimals Genetically ModifiedNeuroblastPrecursor cellGlial cellsmedicineHomeoboxAnimalsDrosophila ProteinsCell LineageMolecular BiologyBody PatterningGeneticsHomeodomain ProteinsNeuronsbiologyGene Expression Regulation DevelopmentalCell DifferentiationCell Biologybiology.organism_classificationLadybirdCell biologymedicine.anatomical_structureDrosophila melanogasternervous systemVentral nerve cordIdentity specificationHomeoboxNeurogliaDrosophilaDrosophila melanogasterCNSNeurogliaDrosophila ProteinTranscription FactorsDevelopmental BiologyDevelopmental Biology
researchProduct

Differentiation of Type 1 ILCs from a Common Progenitor to All Helper-like Innate Lymphoid Cell Lineages

2014

SummaryInnate lymphoid cells (ILCs) are a recently recognized group of lymphocytes that have important functions in protecting epithelial barriers against infections and in maintaining organ homeostasis. ILCs have been categorized into three distinct groups, transcriptional circuitry and effector functions of which strikingly resemble the various T helper cell subsets. Here, we identify a common, Id2-expressing progenitor to all interleukin 7 receptor-expressing, “helper-like” ILC lineages, the CHILP. Interestingly, the CHILP differentiated into ILC2 and ILC3 lineages, but not into conventional natural killer (cNK) cells that have been considered an ILC1 subset. Instead, the CHILP gave rise…

Cellular differentiationLineage (evolution)Bone Marrow CellsGATA3 Transcription FactorBiologyGeneral Biochemistry Genetics and Molecular BiologyMicemedicineAnimalsLymphocytesskin and connective tissue diseasesProgenitorInhibitor of Differentiation Protein 2Receptors Interleukin-7Biochemistry Genetics and Molecular Biology(all)Intracellular parasiteStem CellsInnate lymphoid cellNFIL3Cell DifferentiationT helper cellImmunity InnateMice Inbred C57BLbody regionsmedicine.anatomical_structureImmunologyToxoplasmaIntracellularToxoplasmosisCell
researchProduct

Isolation and characterization of a murine resident liver stem cell.

2008

Increasing evidence provides support that mammalian liver contains stem/progenitor cells, but their molecular phenotype, embryological derivation, biology and their role in liver cell turnover and regeneration remain to be further clarified. In this study, we report the isolation, characterization and reproducible establishment in line of a resident liver stem cell (RLSC) with immunophenotype and differentiative potentiality distinct from other previously described liver precursor/stem cells. RLSCs, derived from fetal and neonatal murine livers as well as from immortalized hepatocytic MMH lines and established in lines, are Sca+, CD34-, CD45-, alpha-fetoprotein+ and albumin-. This molecular…

Cellular differentiationLiver Stem CellCell SeparationBiologyImmunophenotypingLiver progenitor cellsMiceChondrocyteshepatocyteAnimalsCell LineageProgenitor cellLiver progenitor cells; hepatocyte; differentiationMolecular BiologyCells CulturedMultipotent Stem CellOligonucleotide Array Sequence AnalysisNeuronsOsteoblastsAnimalOligonucleotide Array Sequence AnalysiLiver cellOsteoblastGene Expression ProfilingMultipotent Stem CellsMesenchymal stem cellCell DifferentiationCell BiologydifferentiationNeuronChondrocyteMolecular biologyLiver regenerationCell biologyPhenotypeAnimals NewbornLiverMultipotent Stem CellHepatocytesStem cellAnimals; Animals Newborn; Cell Differentiation; Cell Lineage; Cell Separation; Cells Cultured; Chondrocytes; Gene Expression Profiling; Hepatocytes; Immunophenotyping; Liver; Mice; Multipotent Stem Cells; Neurons; Oligonucleotide Array Sequence Analysis; Osteoblasts; Phenotype; Molecular Biology; Cell BiologyCell death and differentiation
researchProduct

Evidence for a common progenitor of epithelial and mesenchymal components of the liver

2013

Tissues of the adult organism maintain the homeostasis and respond to injury by means of progenitor/stem cell compartments capable to give rise to appropriate progeny. In organs composed by histotypes of different embryological origins (e.g. The liver), the tissue turnover may in theory involve different stem/precursor cells able to respond coordinately to physiological or pathological stimuli. In the liver, a progenitor cell compartment, giving rise to hepatocytes and cholangiocytes, can be activated by chronic injury inhibiting hepatocyte proliferation. The precursor compartment guaranteeing turnover of hepatic stellate cells (HSCs) (perisinusoidal cells implicated with the origin of the …

Cellular differentiationLiver Stem CellDesminMice0302 clinical medicineMESH: AnimalsMESH: Nerve Tissue ProteinsHepatic stellate cellCells Cultured0303 health sciencesMesenchymal Stromal CellStem CellsCell DifferentiationCell biologyEndothelial stem cellMESH: DesminMESH: Models AnimalLiverMESH: Epithelial CellsDifferentiationModels Animal030211 gastroenterology & hepatologyStem cellMESH: Stem Cell Transplantationhepatic stellate cell; cell transplantation; liver stem cell; differentiationMESH: Cells CulturedMESH: Cell DifferentiationCell transplantation; Differentiation; Hepatic stellate cell; Liver stem cell; Animals; Cell Differentiation; Cell Line; Cell Lineage; Cell Proliferation; Cells Cultured; Desmin; Epithelial Cells; Glial Fibrillary Acidic Protein; In Vitro Techniques; Liver; Mesenchymal Stromal Cells; Mice; Mice Nude; Models Animal; Nerve Tissue Proteins; Stem Cell Transplantation; Stem Cells; Cell Biology; Molecular BiologyClinical uses of mesenchymal stem cellsMice NudeNerve Tissue ProteinsMESH: Stem Cells[SDV.BC]Life Sciences [q-bio]/Cellular BiologyBiologyIn Vitro TechniquesCell Line03 medical and health sciencesStem CellMESH: Cell ProliferationGlial Fibrillary Acidic ProteinMESH: Mice NudeAnimalsCell LineageProgenitor cellMESH: MiceMolecular Biology030304 developmental biologyCell ProliferationOriginal PaperEpithelial CellAnimalIn Vitro TechniqueMesenchymal stem cellEpithelial CellsMesenchymal Stem CellsCell BiologyMESH: Cell LineageMESH: Cell LineLiver stem cellNerve Tissue ProteinHepatic stellate cellMESH: Mesenchymal Stromal CellsCell transplantationMESH: LiverStem Cell Transplantation
researchProduct

EGF converts transit-amplifying neurogenic precursors in the adult brain into multipotent stem cells.

2002

AbstractNeural stem cells in the subventricular zone (SVZ) continue to generate new neurons in the adult brain. SVZ cells exposed to EGF in culture grow to form neurospheres that are multipotent and self-renewing. We show here that the majority of these EGF-responsive cells are not derived from relatively quiescent stem cells in vivo, but from the highly mitotic, Dlx2+, transit-amplifying C cells. When exposed to EGF, C cells downregulate Dlx2, arrest neuronal production, and become highly proliferative and invasive. Killing Dlx2+ cells dramatically reduces the in vivo response to EGF and neurosphere formation in vitro. Furthermore, purified C cells are 53-fold enriched for neurosphere gene…

Cellular differentiationNeuroscience(all)Mice TransgenicBiology03 medical and health sciencesMice0302 clinical medicineCell MovementNeurosphereSpheroids CellularAnimalsCell LineageCells Cultured030304 developmental biologyHomeodomain ProteinsNeurons0303 health sciencesEpidermal Growth FactorGeneral NeuroscienceStem CellsBrainCell DifferentiationImmunohistochemistryNeural stem cellCell biologyUp-RegulationNeuroepithelial cellEndothelial stem cellErbB ReceptorsMicroscopy ElectronPhenotypenervous systemMultipotent Stem CellAstrocytesStem cellNeuroscience030217 neurology & neurosurgeryCell DivisionAdult stem cellTranscription FactorsNeuron
researchProduct