8 research outputs found

    Stable cell line of T-SV40 immortalized human glomerular visceral epithelial cells

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    Stable cell line of T-SV40 immortalized human glomerular visceral epithelial cells. Human subcultures (third passage) of glomerular visceral epithelial cells (VEC) isolated from one month old kidney were successfully transfected by two recombinant plasmids containing the cloned oncogenes from the simian virus 40 large T antigen and H-ras gene. One postcrisis cell clone (56/10 A1) was selected, propagated and characterized. One hundred percent of the 56/10 A1 cells (current passage > 100th; doubling time 30 hrs) expressed the nuclear T-SV40 antigen assayed by IF; the cells failed to express H-ras (RNA blot analysis). Immortalized cells were morphologically and phenotypically compared to parental cell type (third passage). Phenotypic characterization of the 56/10 Al cells was achieved using indirect immunofluorescence (IF) and immunogold silver staining coupled to bright field and epipolarization microscopy. Both parental and 56/10 A1 cells displayed positivity for cytokeratin, CALLA and PHM5, whereas von Willebrand factor was not detected in the two cell types. Since we have previously shown that human glomerular epithelial cells in culture synthetize plasminogen activator (PA) related compounds, we investigated the secretion pattern of these products in parental and transfected cells. Zymographic analysis of secreted PA related compounds revealed production of free urokinase (u-PA) and type 1 plasminogen activator inhibitor (PAI-1) complexed to tissular plasminogen activator (t-PA). Finally, in the transfected cells, increased cGMP generation under atrial natriuretic factor (ANF) stimulation agreed with previous work performed on nontransfected human VEC. In conclusion, the establishment of a human permanent cell line which retains most of the phenotypic features of parental glomerular visceral epithelial cells should represent a new tool to study human glomerular cell functions

    Adenoma Detection by Endocuff-Assisted versus Standard Colonoscopy in Routine Practice: A Cluster-Randomised Crossover Trial

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    International audienceOBJECTIVE: Endocuff Vision (ECV) is the second generation of a device designed to improve polyp detection. The aim of this study was to evaluate its impact on adenoma detection rate (ADR) in routine colonoscopy. DESIGN: This cluster-randomised crossover trial compared Endocuff-assisted (ECV+) with standard (ECV-) colonoscopy. Two teams of 11 endoscopists each with prior ECV experience, balanced in terms of basal ADR, gender and case volume were compared. In randomised fashion, the teams started with ECV+ or ECV- and switched group after inclusion of half of the cases. The main outcome criterion was ADR difference between ECV+ and ECV-. Subgroup analysis was done for physicians with low and high ADR (< or ≥q 25%). RESULTS: During two periods of 20 and 21 weeks, respectively, the 22 endoscopists included 2058 patients (1032 ECV- vs 1026 ECV+, both groups being comparable). Overall ADR for both groups taken together was higher with ECV (39.2%) than without (29.4%; p<0.001) irrespective of the sequence of use (ECV+ or ECV- first), but mostly in adenomas <1\,cm. In the physician subgroup analysis, only high detectors showed a significant ADR increase (from 31% to 41%, p<0.001), while the increase in the low detectors was not significant (from 24% to 30%, p=0.11). ECV had a positive impact in all colonic locations, except for the rectum. No ECV- related complication was reported. CONCLUSION: We observed a significant ADR difference of approximately 10% by the use of ECV. By subgroup analysis, this increase was significant only in physicians classified as high detectors. TRIAL REGISTRATION NUMBER: ClinicalTrials.gov (NCT03344055)

    Quelle Ă©ducation avec la Covid-19

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    APPEL A CONTRIBUTION : QUE NOUS APPREND LA PANDEMIE? NumĂ©ro HS Recherches et Educations (Juillet 2020) (HCERES 70ème section) Qu'est ce que la pandĂ©mie nous apprend de nos sociĂ©tĂ©s, de nos politiques de santĂ© publique, des souverainetĂ©s Ă©pistĂ©mologiques de la recherche et des praxis individuelles et collectives? SolidaritĂ©s ou/ et d'exclusions? StratĂ©gies d'adaptation au confinement ou de rejet? Comment agit-on dans ce monde incertain, soumis Ă  l'autoritĂ© des politiques de gestion d'un virus? Soumission volontaire Ă  l'autoritĂ© ou organisation des rĂ©sistances? Quels sont les savoirs exercĂ©s sur quels pouvoirs ? Quelles sont les lĂ©gitimitĂ©s et les responsabilitĂ©s plurielles : individuelles, collectives, politiques et sociales ? Quels sont les usages sociaux et politiques des rĂ©sultats de la recherche des experts ? Qu’apprenons nous des expĂ©riences de prĂ©vention individuelles, europĂ©ennes et internationales ? Comment s’exercent les pouvoirs Ă  partir des savoirs des Ă©pistĂ©mologies et des Ă©vidence-base medecine ? Comment l’histoire des Ă©pidĂ©mies pourrait rĂ©pondre Ă  notre prĂ©sent ? Quel futur pour notre sociĂ©tĂ© après la pandĂ©mie ? Quelles seront nos inĂ©galitĂ©s sociales ? Vers quelles Ă©cologies ? Quelles rĂ©sistances ? Quel mode de vie ? Quelles expĂ©riences corporelles de l’absence de toucher et de la distanciation ? Quelle croissance ? Quelle dĂ©croissance ? Quelles solidaritĂ©s face Ă  la techno-Ă©conomique ? La revue Recherches & Educations lance un appel Ă  contribution, multi disciplinaire, sur le « dispositif covid 19 » pendant le confinement imposĂ© aux populations. Elle propose de rĂ©unir les textes critiques et rĂ©flexifs sur ce que nous apprend l’épidĂ©mie et la pandĂ©mie de nous mĂŞme, de notre relation au vivant, Ă  la mondialisation nĂ©olibĂ©rale, aux souverainetĂ©s de santĂ©, au gouvernement des corps, de la psychĂ© et de la vie, aux politiques de prĂ©vention, aux reprĂ©sentations de l’épidĂ©mie, aux pratiques corporelles visuelles et tactiles, aux modes de rĂ©sistances et aux praxis du quotidien du prĂ©sent et de demain. Texte Ă  adresser (avant le 30 mai 2020) en 30.000 signes Ă  [email protected] [email protected] [email protected]
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