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Effects of long-term serial cell passaging on cell spreading, migration, and cell-surface ultrastructures of cultured vascular endothelial cells

机译:长期连续传代对培养的血管内皮细胞的细胞扩散,迁移和细胞表面超微结构的影响

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The effects of serial cell passaging on cell spreading, migration, and cell-surface ultrastructures have been less investigated directly. This study evaluated the effects of long-term serial cell passaging (totally 35 passages) on cultured human umbilical vein endothelial cells which were pre-stored at ?80?°C as usual. Percentage- and spread area-based spreading assays, measurements of fluorescently labeled actin filaments, migration assay, and measurements of cell-surface roughness were performed and quantitatively analyzed by confocal microscopy or atomic force microscopy. We found that the abilities of cell spreading and migration first increased at early passages and then decreased after passage 15, in agreement with the changes in average length of actin filaments. Recovery from cold storage and effects of cell passaging were potentially responsible for the increases and decreases of the values, respectively. In contrast, the average roughness of cell surfaces (particularly the nucleus-surrounding region) first dropped at early passages and then rose after passage 15, which might be caused by cold storage- and cell passaging-induced endothelial microparticles. Our data will provide important information for understanding serial cell passaging and implies that for pre-stored adherent cells at ?80?°C cell passages 5–10 are optimal for in vitro studies.
机译:很少直接研究连续细胞传代对细胞扩散,迁移和细胞表面超微结构的影响。这项研究评估了长期连续的细胞传代(总共35传)对培养的人脐静脉内皮细胞的影响,这些细胞通常被保存在80°C下。进行了基于百分比和扩散区的扩散测定,荧光标记肌动蛋白丝的测定,迁移测定以及细胞表面粗糙度的测定,并通过共聚焦显微镜或原子力显微镜进行了定量分析。我们发现细胞扩散和迁移的能力首先在早期传代时增加,然后在传代15后降低,这与肌动蛋白丝平均长度的变化一致。从冷库中恢复和细胞传代的影响可能分别导致值的增加和减少。相比之下,细胞表面(尤其是细胞核周围区域)的平均粗糙度在早期传代时先下降,然后在传代15次后便上升,这可能是由冷藏和细胞传代诱导的内皮微粒引起的。我们的数据将为理解连续细胞传代提供重要信息,并暗示对于80°C时预存的贴壁细胞,5-10次传代是体外研究的最佳选择。

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