Search results for "Mesoangioblasts"

showing 10 items of 13 documents

Autophagy and apoptosis regolate survival of mesoangioblast stem cells subjected to oxidative stress

2012

Autophagy apoptosis mesoangioblasts oxidative stressSettore BIO/06 - Anatomia Comparata E Citologia
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Stress response in mesoangioblast stem cells

2006

Stem cells are presumed to survive various stresses, since they are recruited to areas of tissue damage and regeneration, where inflammatory cytokines and cytotoxic cells may result in severe cell injury. We explored the ability of mesoangioblasts to respond to different cell stresses such as heat, heavy metals and osmotic stress, by analyzing heat shock protein (HSP)70 synthesis as a stress indicator. We found that the A6 mesoangioblast stem cells constitutively synthesize HSP70 in a heat shock transcription factor (HSF)-independent way. However, A6 respond to heat shock and cadmium treatment by synthesizing HSP70 over the constitutive expression and this synthesis is HSF1 dependent. The e…

Chloramphenicol O-AcetyltransferaseHot TemperatureOsmotic shockRecombinant Fusion ProteinsBlotting WesternHypertonic SolutionsElectrophoretic Mobility Shift AssayBiologyResponse ElementsTransfectionMesodermMiceSTRESS RESPONSE STEM CELLS MOUSE MESOANGIOBLASTS.Heat Shock Transcription FactorsHeat shock proteinMetals HeavyAnimalsRNA MessengerHSF1Promoter Regions GeneticMolecular BiologyCells CulturedMesoangioblastHSC70 Heat-Shock ProteinsCell BiologyTransfectionHematopoietic Stem CellsMolecular biologyCell biologyHsp70Heat shock factorDNA-Binding ProteinsGene Expression RegulationStem cellTranscription Factors
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Hsp70 level regulates MMP2 expression in mesoangioblast stemj cells

2013

Hsp70 mesoangioblasts stem cells MMP2
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MMP2 synthesis in mouse mesoangioblast stem cells is highly regulated

2012

MMP2 stem cells mesoangioblastsSettore BIO/06 - Anatomia Comparata E Citologia
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High-density ZnO Nanowires as a Reversible Myogenic-Differentiation-Switch

2018

Mesoangioblasts are outstanding candidates for stem-cell therapy and are already being explored in clinical trials. However, a crucial challenge in regenerative medicine is the limited availability of undifferentiated myogenic progenitor cells because growth is typically accompanied by differentiation. Here reversible myogenic-differentiation switching during proliferation is achieved by functionalizing the glass substrate with high-density ZnO nanowires (NWs). Specifically, mesoangioblasts grown on ZnO NWs present a spherical viable undifferentiated cell state without lamellopodia formation during the entire observation time (8 days). Consistently, the myosin heavy chain, typically express…

Myogenic differentiationMaterials scienceCellmuscle differentiation02 engineering and technologyMuscle Development010402 general chemistrySettore BIO/0901 natural sciencesRegenerative medicineZnO nanowireZnO nanowires; mesoangioblasts; muscle differentiation; tissue engineeringTissue engineeringmesoangioblastsMyosinmedicinemesoangioblastGeneral Materials ScienceProgenitor cellNanowiresZno nanowiresSubstrate (chemistry)Cell Differentiation021001 nanoscience & nanotechnology0104 chemical sciencesCell biologymedicine.anatomical_structuretissue engineeringZnO nanowiresZinc Oxide0210 nano-technology
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Porous PLLA scaffolds are optimal substrates for internal colonization by A6 mesoangioblasts and immunocytochemical analyses

2009

In the present paper, mouse mesoangioblasts were seeded onto bidimensional matrices and within three-dimensional porous scaffolds of poly(L-lactic acid) (PLLA), in the presence or absence of type I collagen coating, observed under the scanning electron microscope, and tested for their adhesion, survival and proliferation. Immunolocalization of Hsp70, an abundant and ubiquitous intracellular protein in these cells, was also performed in sectioned cell-containing scaffolds under the confocal fluorescence microscope to check whether "in situ" analysis of intracellular constituents was feasible. The data obtained show that PLLA films allow direct cell adhesion and represent an optimal support f…

PLLA mesoangioblastsSettore BIO/06 - Anatomia Comparata E Citologia
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Ku factor is responsible of Hsp70 basal transcription in mouse mesoangioblasts

2008

Settore BIO/06 - Anatomia Comparata E CitologiaKu factor Hsp70 mesoangioblasts
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Mouse mesoangioblasts release Hsp70 in a controlled manner through membrane vesicle shedding

2009

Mesoangioblaststs (Mabs) are mesodermal stem cells associated with vessels which can differentiate into different mesoderm cell types. They have the property to cross endothelial barrier and when injected into circulation they localize into damaged tissues. A6 cells, a clone of mouse Mabs, express Hsp70 protein in physiological conditions and this synthesis may be required to answer to several intra- and/or extra-cellular needs. It was found that Hsp70 may be released outside from several type of cells, but its role remains still undefined. In order to clarify the reason of Hsp70 constitutive expression, we prepared several A6 clones with different levels of Hsp70 expression by stable RNA i…

Settore BIO/06 - Anatomia Comparata E CitologiaMesoangioblasts Hsp70 membrane vesicles
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Paracrine effect of membrane vesicles released by mouse mesoangioblast stem cells on non correlated cell types

2016

Introduction Mouse mesoangioblasts are vessel-associated multipotent progenitor stem cells, which are able to differentiate into different mesodermal cell types. In our previous paper we have demonstrated that these cells are able to shed in the extracellular environment membrane vesicles (EV), which contain both structural proteins and biological factors such as FGF2 and the two gelatinases MMP2/9. EV represent an important mediator of cell-to-cell communication and are involved in both autocrine and paracrine signalling. Interestingly, there is a bidirectional signalling exchange between stem cell EV and damaged cells. In particular, EV from injured cells can reprogram stem cells to acqui…

Stem cells mesoangioblasts membrane vesicles migration. macrophages endothelial cells.
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Mouse mesoangioblast behaviour when subjected to cellular stress

2009

cellular stress stem cells mouse mesoangioblastsSettore BIO/06 - Anatomia Comparata E Citologia
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