首页> 外文期刊>Biochimica et biophysica acta. Molecular cell research >Role of clusterin in cell adhesion during early phases of programmed cell death in PI9 embryonic carcinoma cells
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Role of clusterin in cell adhesion during early phases of programmed cell death in PI9 embryonic carcinoma cells

机译:在PI9胚胎癌细胞程序性细胞死亡的早期阶段,簇蛋白在细胞粘附中的作用

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摘要

This study explored the role of clusterin in mechanisms of cell adhesion and apoptosi.s in P19 embryonic carcinoma cells. We found that serum deprivation induced transient but dramatic elevation in cell adhesion strength to the culture substrate and eventually led to apoptotic cell death. The lime course of cell-adhesion increase overlapped temporally with the elevation of clusterin mRNA (peak 8 h after serum deprivation). The coincidental elevation of clusterin expression and cell adhesion strength preceded the schedule of apoptotic cell death. Clusterin antiserum partially antagonized cell adhesion, but did not modify the course of apoptosis. These data suggest that clusterin expression may partially control cell adhesion with no influence on apoptosis in PI9 cells, under defined conditions.
机译:这项研究探讨了簇蛋白在P19胚胎癌细胞的细胞黏附和凋亡机制中的作用。我们发现血清剥夺诱导细胞粘附于培养基质的瞬时但显着升高,并最终导致凋亡性细胞死亡。细胞粘附的石灰过程在时间上与簇蛋白mRNA的升高重叠(血清剥夺后8小时峰值)。簇蛋白表达和细胞粘附强度的同时升高在凋亡细胞死亡的时间表之前。簇蛋白抗血清部分拮抗细胞粘附,但不改变细胞凋亡过程。这些数据表明,在确定的条件下,簇蛋白的表达可以部分控制细胞粘附,而不影响PI9细胞的凋亡。

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