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Linear Loading Cryoprotectants (CPAs) With Microfluidic Method Reduces Osmotic Damage to Porcine M II-stage Oocytes

文献类型: 外文期刊

作者: Yang Yun 1 ; Zhou Xin-Li 1 ; Dai Jian-Jun 2 ; Zhang De-Fu 2 ; Shag Wen-Qi 1 ; Yi Xing-Yue 1 ; Tao Le-Ren 1 ;

作者机构: 1.Univ Shanghai Sci & Technol, Inst Biothermal Technol, Shanghai 200093, Peoples R China

2.Shanghai Acad Agr Sci, Inst Anim Husb & Vet Sci, Shanghai 201106, Peoples R China

关键词: oocyte;microfluidics;osmotic damage;CPA;cryopreservation

期刊名称:PROGRESS IN BIOCHEMISTRY AND BIOPHYSICS ( 影响因子:0.351; 五年影响因子:0.272 )

ISSN: 1000-3282

年卷期: 2016 年 43 卷 6 期

页码:

收录情况: SCI

摘要: Loading cryoprotectants (CPAs) into oocytes is critical to restrain ice formation during cryopreservation. However, high concentration of CPAs may cause osmotic and toxic damage to oocytes. In order to minimize the osmotic damage, a microfluidic device for loading CPAs into oocytes was designed and fabricated in this study. 30% (vlv) Me2SO was linear loaded into porcine M II-stage oocyte with the microfluidic device, the intracellular CPA concentration, the cell volumetric changes and the effect on the survival rate and developmental rate of oocytes were investigated and compared with the traditional methods including the one-step method and the step-wise methods. The results showed that the microfluidic method can realize continuous CPA loading to oocytes, reduce the osmotic shock to cells and enhance the cell viability. The lowest penetration volume of oocyte reached 0.86V(0). The cell viability was 92.8% with the microfluidic method, similar to 33% higher than one-step method, similar to 16.3% higher than two-step method, and no significant difference with four-step method. After parthenogenetic activation and cultured in vitro, the cleavage rate and the blastocyst rate of oocytes were 75.8% and 27.4%, which were significantly higher than the one-step method and the step-wise methods (P < 0.05). In conclusion, linear loading CPAs with the microfluidic method can significantly alleviate the osmotic damage to oocytes, which may provide a new path for oocyte cryopreservation.

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