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Comparison of senescence progression in mesenchymal cells from human umbilical cord walls measured by immunofluorescence and flow cytometry of p16 and p21

机译:通过免疫荧光和P21流式细胞仪测量的人脐脐带间充质细胞衰老进展的比较

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OBJECTIVE:To follow the expansion of mesenchymal stem cells from umbilical cords by two classic senescence markers, p16 (INK4A) and p21 (CDKN1A), using practical, fast, and less expensive methods than the gold standard Western blotting technique, to evaluate its applicability in the laboratory.METHODS:Mesenchymal stem cells from umbilical cords were isolated from Wharton's jelly and, after quality control, morphological and immunophenotypic characterization by flow cytometry, were expanded in culture until coming close to cell cycle arrest (replicative senescence).RESULTS:A comparison was made between young cells, at passage 5, and pre-senescent cells, at passage 10, evaluating the protein expression of the classic cell senescence markers p16 and p21, comparing the results obtained by Western blotting with those obtained by flow cytometry and indirect immunofluorescence.CONCLUSION:Follow-up of cell cultures, through indirect p16 immunofluorescence, allows the identification of mesenchymal stem cells from umbilical cord cultures at risk of reaching replicative senescence.
机译:目的:使用两种经典衰老标记,P16(INK4A)和P21(CDKN1A)遵循从脐带的间充质干细胞的扩增,使用实用,快速,更便宜的方法,而不是金标准的Western印迹技术,以评估其适用性在实验室中,方法:来自脐带的间充质干细胞从沃顿果冻中分离出来,并且在质量控制,通过流式细胞术中的形态学和免疫型特性进行,在培养基中扩增,直至接近细胞周期停滞(复制衰老)。结果:a在通过10的通道10中,在通道5和衰老细胞处,评估经典细胞衰老标记物P16和P21的蛋白质表达的比较,比较通过蛋白质印迹获得的结果与通过流式细胞术和间接获得的结果免疫荧光。结论:通过间接P16免疫荧光进行细胞培养物的随访,允许鉴定苦度来自脐带培养物的MAL干细胞,风险达到复制衰老。

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