0000000000679218

AUTHOR

Catherine M. Verfaillie

0000-0001-7564-4079

showing 7 related works from this author

In vitro and in vivo arterial differentiation of human multipotent adult progenitor cells

2006

Many stem cell types have been shown to differentiate into endothelial cells (ECs); however, their specification to arterial or venous endothelium remains unexplored. We tested whether a specific arterial or venous EC fate could be induced in human multipotent adult progenitor cells (hMAPCs) and AC133(+) cells (hAC133(+)). In vitro, in the presence of VEGF(165), hAC133(+) cells only adopted a venous and microvascular EC phenotype, while hMAPCs differentiated into both arterial and venous ECs, possibly because hMAPCs expressed significantly more sonic hedgehog (Shh) and its receptors as well as Notch 1 and 3 receptors and some of their ligands. Accordingly, blocking either of those pathways …

Vascular Endothelial Growth Factor ACellular differentiationImmunologyMice NudeNeovascularization PhysiologicCell SeparationBiochemistryMiceAntigens CDAnimalsHumansHedgehog ProteinsAC133 AntigenSonic hedgehogProgenitor cellNotch 1Cells CulturedGlycoproteinsMatrigelbiologyReceptors NotchEndothelial CellsCell DifferentiationCell BiologyHematologyPeptide FragmentsCell biologyEndothelial stem cellAdult Stem CellsMicroscopy ElectronImmunologybiology.proteinStem cellPeptidesAdult stem cellSignal Transduction:Ciencias de la Salud::Oncología [Materias Investigacion]
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Effects of MRI Contrast Agents on the Stem Cell Phenotype

2010

The ultimate therapy for ischemic stroke is restoration of blood supply in the ischemic region and regeneration of lost neural cells. This might be achieved by transplanting cells that differentiate into vascular or neuronal cell types, or secrete trophic factors that enhance self-renewal, recruitment, long-term survival and functional integration of endogenous stem/progenitor cells. Experimental stroke models have been developed to determine potential beneficial effect of stem/progenitor cell based therapies. To follow the fate of grafted cells in vivo, a number of non-invasive imaging approaches have been developed. Magnetic Resonance Imaging (MRI) is a high resolution, clinically relevan…

MaleCell typePopulationBiomedical EngineeringContrast Medialcsh:MedicineBiology03 medical and health sciencesMice0302 clinical medicineIn vivoCell MovementAnimalsProgenitor celleducationMagnetite NanoparticlesEmbryonic Stem Cells030304 developmental biology0303 health sciencesTransplantationeducation.field_of_studyRegeneration (biology)Multipotent Stem CellsMesenchymal stem celllcsh:RCell DifferentiationDextransMesenchymal Stem CellsCell BiologyFlow CytometryEmbryonic stem cellMagnetic Resonance Imaging3. Good healthCell biologyRatsStrokePhenotypeFemaleStem cell030217 neurology & neurosurgeryCell Transplantation
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Regulation of hematopoiesis through adhesion receptors

2001

Normal steady-state hematopoiesis takes place in the bone marrow microenvironment. Soluble factors as well as contact interactions between the hematopoietic cells and the marrow microenvironment dictate the fate of hematopoietic stem cells and progenitors. Over the last decade it has become clear that cell-cell and cell-extracellular matrix interactions through adhesion receptors play a major role in the hematopoietic process. They are required for the residence of stem cells and progenitors in the marrow, as well as for homing of stem and progenitor cells to the marrow in the setting of stem cell transplantation. Furthermore, adhesion receptors play an important role in regulation of cell …

ImmunologyMembrane ProteinsBone Marrow CellsStem cell factorCell BiologyBiologyHematopoietic Stem CellsHematopoietic ProcessHematopoiesisCell biologyEndothelial stem cellmedicine.anatomical_structureCell AdhesionmedicineAnimalsHumansImmunology and AllergyBone marrowStem cellProgenitor cellCell adhesionHoming (hematopoietic)
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Thymidine analogs are transferred from prelabeled donor to host cells in the central nervous system after transplantation: a word of caution

2006

Thymidine analogs, including bromodeoxyuridine, chlorodeoxyuridine, iododeoxyuridine, and tritiated thymidine, label dividing cells by incorporating into DNA during S phase of cell division and are widely employed to identify cells transplanted into the central nervous system. However, the potential for transfer of thymidine analogs from grafted cells to dividing host cells has not been thoroughly tested. We here demonstrate that graft-derived thymidine analogs can become incorporated into host neural precursors and glia. Large numbers of labeled neurons and glia were found 3-12 weeks after transplantation of thymidine analog-labeled live stem cells, suggesting differentiation of grafted ce…

Central Nervous SystemCell divisionCentral nervous systemBiological Transport ActiveMice TransgenicIn Vitro TechniquesBiologyRats Sprague-Dawleychemistry.chemical_compoundMicePregnancyRats Inbred SHRmedicineAnimalsCell ProliferationNeuronsCell growthBrainCell BiologyMolecular biologyRatsTransplantationmedicine.anatomical_structurechemistryAnimals NewbornBromodeoxyuridineMolecular MedicineNeurogliaFemaleStem cellThymidineNeurogliaBromodeoxyuridineDevelopmental BiologyStem Cell TransplantationThymidine
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Therapeutic effects of hMAPC and hMSC transplantation after stroke in mice.

2012

Stroke represents an attractive target for stem cell therapy. Although different types of cells have been employed in animal models, a direct comparison between cell sources has not been performed. The aim of our study was to assess the effect of human multipotent adult progenitor cells (hMAPCs) and human mesenchymal stem cells (hMSCs) on endogenous neurogenesis, angiogenesis and inflammation following stroke. BALB/Ca-RAG 2(-/-) γC(-/-) mice subjected to FeCl(3) thrombosis mediated stroke were intracranially injected with 2 × 10(5) hMAPCs or hMSCs 2 days after stroke and followed for up to 28 days. We could not detect long-term engraftment of either cell population. However, in comparison w…

MaleAnatomy and PhysiologyMousemedicine.medical_treatmentCell therapyMiceCell MovementMolecular Cell BiologyNeurobiology of Disease and RegenerationMedicineMultidisciplinaryNeuronal MorphologyNeurogenesisQRBrainInfarction Middle Cerebral ArteryAnimal ModelsStem-cell therapyStrokeAdult Stem Cellsmedicine.anatomical_structureNeurologyMedicineResearch ArticleAdult stem cellCell PhysiologyHistologyCell SurvivalCerebrovascular DiseasesScienceTherapeutic effectsNeurophysiologyNeovascularization PhysiologicSubventricular zoneMesenchymal Stem Cell TransplantationNeurological SystemModel OrganismsAnimalsHumansProgenitor cellBiologyTransplantationbusiness.industryMultipotent Stem CellsMesenchymal stem cellMultipotent Stem CellCellular NeuroscienceImmunologyCancer researchMolecular NeurosciencebusinesshMAPC and hMSCNeurosciencePLoS ONE
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BrdU is not a reliable label for transplanted cells in the central nervous system

2006

medicine.anatomical_structureDevelopmental NeuroscienceNeurologyCentral nervous systemmedicineBiologyBiological systemNeuroscienceExperimental Neurology
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Contribution of different bone marrow-derived cell types in endometrial regeneration using an irradiated murine model.

2015

Objective To study the involvement of seven types of bone marrow-derived cells (BMDCs) in the endometrial regeneration in mice after total body irradiation. Design Prospective experimental animal study. Setting University research laboratories. Animal(s) β-Actin-green fluorescent protein (GFP) transgenic C57BL/6-Tg (CAG-EGFP) and C57BL/6J female mice. Intervention(s) The BMDCs were isolated from CAG-EGFP mice: unfractionated bone marrow cells, hematopoietic progenitor cells, endothelial progenitor cells (EPCs), and mesenchymal stem cells (MSCs). In addition three murine GFP + cell lines were used: mouse Oct4 negative BMDC multipotent adult progenitor cells (mOct4 − BM-MAPCs), BMDC hypoblast…

Pathologymedicine.medical_specialtyStromal cellBone Marrow CellsBiologyEndometriumMicemedicineAnimalsRegenerationProgenitor cellCells CulturedMesenchymal stem cellObstetrics and GynecologyCell DifferentiationMesenchymal Stem CellsTotal body irradiationMolecular biologyBone Marrow-Derived CellTransplantationMice Inbred C57BLmedicine.anatomical_structureReproductive MedicineFemaleBone marrowStem cellWhole-Body IrradiationFertility and sterility
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