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p53基因缺陷会加剧胰腺腺泡细胞转分化过程中多向性有丝分裂缺陷、核型变化及多倍体形成。

p53 deficiency exacerbates pleiotropic mitotic defects, changes in nuclearity and polyploidy in transdifferentiating pancreatic acinar cells.

作者信息

Sphyris Nathalie, Harrison David J

机构信息

Division of Pathology, School of Molecular and Clinical Medicine, The University of Edinburgh, Teviot Place, Edinburgh EH8 9AG, UK.

出版信息

Oncogene. 2005 Mar 24;24(13):2184-94. doi: 10.1038/sj.onc.1208249.

Abstract

In a primary culture model for pancreatic acinar-ductal transdifferentiation, cells exhibited increased proliferation, changes in nuclearity and polyploidy. We identify the 'nucleus to centrosome' ratio of the progenitor cell, the dissemination of centrosomes at spindle poles and cytokinesis failure as critical determinants of mitosis outcome and centrosome inheritance. Abortive cytokinesis of mononuclear cells contributes to the binuclear cell pool, whereas enclosure of entire mitotic formations, within a single nuclear envelope, perpetuates polyploidization. Binuclear cell nuclei combine their genomes on a single metaphase plate, doubling descendant ploidy. Moreover, approximately 42% of binuclear and tetraploid cells assemble aberrant spindles with up to 8 centrosomes/poles. These phenotypes were exacerbated in p53-deficient cultures exhibiting increased S-phase entry, giant nuclei, multinucleation, multipolar mitoses and centrosome hyperamplification. The tendency of p53-proficient cells to spontaneously evade the tetraploidy checkpoint degenerates to uncontrolled polyploid progression in p53-deficient cultures, explaining why p53 abrogation alone rapidly descends to aneuploidy in this system. We detected constitutively nuclear mdm2, which may circumvent endogenous cell-cycle checkpoints, and pronounced accumulation of p21 and p27 in multinuclear cells and giant nuclei, consistent with roles in polyploidization. This in vitro model may recapitulate the processes underlying genomic instability in pancreatic tumours in vivo, and attests to the existence of a p53-dependent polyploidy checkpoint acting to limit the degree of polyploidization.

摘要

在胰腺腺泡-导管转分化的原代培养模型中,细胞表现出增殖增加、核型和多倍体变化。我们确定祖细胞的“细胞核与中心体”比率、中心体在纺锤体极的分布以及胞质分裂失败是有丝分裂结果和中心体遗传的关键决定因素。单核细胞的不完全胞质分裂导致双核细胞池的形成,而整个有丝分裂结构被包裹在单个核膜内会使多倍体化持续存在。双核细胞核在单个中期板上合并它们的基因组,使后代倍性加倍。此外,约42%的双核和四倍体细胞组装异常纺锤体,每个极最多有8个中心体。这些表型在p53缺陷型培养物中加剧,表现为S期进入增加、巨大核、多核化、多极有丝分裂和中心体过度扩增。p53功能正常的细胞自发逃避四倍体检查点的倾向在p53缺陷型培养物中退化为不受控制的多倍体进展,这解释了为什么仅p53缺失在该系统中会迅速导致非整倍体。我们检测到持续存在于细胞核中的mdm2,它可能规避内源性细胞周期检查点,并且在多核细胞和巨大核中p21和p27明显积累,这与它们在多倍体化中的作用一致。这个体外模型可能概括了体内胰腺肿瘤基因组不稳定的潜在过程,并证明存在一个p53依赖的多倍体检查点,其作用是限制多倍体化程度。

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