首页> 外文OA文献 >[Vpliv hipotoničnega pufra in elektroporacije na dinamiko nabrekanja in viabilnost celic za optimizacijo elektrofuzije]
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[Vpliv hipotoničnega pufra in elektroporacije na dinamiko nabrekanja in viabilnost celic za optimizacijo elektrofuzije]

机译:低渗缓冲液和电穿孔对溶胀动力学和细胞活力优化电融合的影响。

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摘要

Background. Various electrofusion parameters have to be adjusted to obtain theoptimal electrofusion efficiency. Based on published data, good electrofusion conditions can be achieved with the hypotonic treatment. However, the duration of the hypotonic treatment before electroporation and buffer hypoosmolarity have to be adjusted in order to cause cell swelling, to avoid regulatory volume decrease and to preserve cell viability. The aims of our study were to determine cell size dynamics and viability of four different cell lines in hypotonic buffer and to study the influence of the electroporation on the selected cell line in hypotonic buffer. Materials and methods. Cell size dynamics of different cell lines exposed to hypotonic buffer and electroporation were analyzed by time-resolvedcell size measurements. The viability of hypotonically treated oržand electroporated cells was determined 24 h after the experiment by a modified crystal violet (CV) viability assay. Results. In our experimental conditions the hypotonic treatment at 100 mOsm was efficient for CHO, V79 and B16-F1 cell lines. The optimal duration of the treatment was between two and five minutes. On the other hand the same hypotonic treatment did not cause cell swelling of NS1 cells. Cell swelling was also observed after electroporation of B16-F1 in isotonic buffer and it was amplified when hypotonic buffer was used. In addition, the regulatory volume decrease was successfully inhibited with electroporation. Conclusions. Cell size dynamicsin hypotonic conditions should be studied for each cell line since they differ in their sensitivity to the hypotonic treatment. The inhibition of cell regulatory volume decrease by electroporation may be beneficial in achieving higher electrofusion efficiency. (Abstract truncated at 2000 characters)
机译:背景。必须调整各种电融合参数以获得最佳电融合效率。根据公开的数据,低渗治疗可达到良好的电融合条件。但是,必须调整电穿孔前的低渗治疗的持续时间和缓冲液低渗性,以引起细胞肿胀,避免调节量减少并保持细胞活力。我们研究的目的是确定低渗缓冲液中四种不同细胞系的细胞大小动力学和活力,并研究低渗缓冲液中电穿孔对所选细胞系的影响。材料和方法。通过时间分辨的细胞大小测量来分析暴露于低渗缓冲液和电穿孔的不同细胞系的细胞大小动态。实验后24小时,通过改良的结晶紫(CV)活力测定法确定经低渗处理的Orzand电穿孔细胞的活力。结果。在我们的实验条件下,对于CHO,V79和B16-F1细胞系,在100 mOsm下进行低渗处理是有效的。治疗的最佳持续时间在两到五分钟之间。另一方面,相同的低渗治疗并未引起NS1细胞的细胞肿胀。在等渗缓冲液中电穿孔B16-F1后,还观察到细胞肿胀,当使用低渗缓冲液时,细胞肿胀被放大。另外,通过电穿孔成功地抑制了调节体积的减少。结论。对于每种细胞系,应研究低渗条件下的细胞大小动态,因为它们对低渗治疗的敏感性不同。通过电穿孔抑制细胞调节体积的减少可能有利于实现更高的电融合效率。 (摘要被截断为2000个字符)

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