|
|
Experimental Study of Linear Removing Cryoprotective Agents from MII Porcine Oocytes with Microfluidics Device |
Zhou Xinli1*, Yang Yun1, Dai Jianjun2, Zhang Defu2, Shao Wenqi1, Yi Xingyue1, Tao Leren1 |
1Institute of Biothermal Technology, University of Shanghai for Science and Technology, Shanghai 200093, China; 2Animal and Veterinary Research Institute, Shanghai Academy of Agricultural Sciences, Shanghai 201106, China |
|
|
Abstract Cryoprotective agents (CPAs) must be removed from cryopreserved oocytes before used in clinic. Step-wise methods usually lead to the cell loss due to complicated operating steps, and may cause fatal osmotic injury to oocytes during CPAs removal process. In order to minimize the osmotic injury to oocytes, a microfluidic device for unloading CPAs from oocytes was designed and fabricated in this study. CPAs were linear unloaded from MII porcine oocytes with microfluidic device under different durations (6 min, 8 min and 10 min), the cell volume changes and the effects on the survival and developmental rate of oocytes were investigated, and then compared with that obtained by the conventional step-wise methods. Results showed that 8 min duration was optimal for linear unloading CPAs with microfluidic device. The linear method remarkably reduced the osmotic injury to oocytes during the removal of CPAs. The highest normalized swelling volume of oocyte only reached 1.12±0.07. The survival, cleavage and blastocyst rate of oocytes were 83.6%, 72.4% and 21.5%,respectively, which were significantly higher than those of one-step method and step-wise methods (P<0.05). In conclusion, linear unloading CPAs with the microfluidic method can significantly alleviate the osmotic damage to oocytes, which may provide a new path for oocyte cryopreservation.
|
Received: 20 September 2016
|
|
|
|
|
[1] Chian RC, Wang Y, Li YR. Oocyte vitrification: advances, progress and future goals [J]. Journal of Assisted Reproduction and Genetics, 2014, 31(4): 411-420. [2] Zhou Xinli, Al-Naib A, Sun Dawen, et al. Bovine oocyte vitrification using the Cryotop method: effect of cumulus cells and vitrification protocol on survival and subsequent development [J]. Cryobiology, 2010, 61(1): 66-72. [3] 李维杰, 周新丽, 刘宝林, 等. 升降温速率对低温保护剂溶液结晶性质的影响 [J]. 化工学报, 2013, 64(8): 2969-2974. [4] Woods EJ, Liu J, Pollok K, et al. A theoretically optimized method for cord blood stem cell cryopreservation [J]. Journal of Hematotherapy & Stem Cell Research, 2003, 12(3): 341-350. [5] 华泽钊,任禾盛. 低温生物医学技术 [M]. 北京:科学出版社, 1994: 166-169. [6] Clark NA, Swain JE. Oocyte cryopreservation: searching for novel improvement strategies [J]. Journal of Assisted Reproduction and Genetics, 2013, 30(7): 865-875. [7] Karlsson JOM, Szurek EA, Higgins AZ, et al. Optimization of cryoprotectant loading into murine and human oocytes [J]. Cryobiology, 2014, 68(1): 18-28. [8] 解政鼎, 马学虎, 艾丹亭, 等. 低温保护剂对神经干细胞球添加过程的模拟分析[J]. 化工学报, 2013, 64(11): 3956-3967. [9] Liu Jun, Mullen S, Meng QG, et al. Determination of oocyte membrane permeability coefficients and their application to cryopreservation in a rabbit model [J]. Cryobiology, 2009, 59(2): 127-134. [10] Liu Jun, Phy J, Yeomeans E. Theoretic considerations regarding slow cooling and vitrification during cryopreservation [J]. Theriogenology, 2012, 78(8): 1641-1652. [11] Coticchio G. Truths and myths of oocyte sensitivity to controlled rate freezing [J]. Reproductive Biomedicine Online, 2007, 15(1): 24-30. [12] 张晓光, 赵刚, 丁卫平, 等. 透析法去除红细胞渗透性低温保护剂的实验研究 [J]. 中国生物医学工程学报, 2008, 27(1): 156-159. [13] Mata C, Longmire EK, Mckenna DH, et al. Experimental study of diffusion-based extraction from a cell suspension [J]. Microfluidics and Nanofluidics, 2008, 5(4): 529-540. [14] Mata C, Longmire EK, Mckenna DH, et al. Cell motion and recovery in a two-stream microfluidic device [J]. Microfluidics and Nanofluidics, 2010, 8(4): 457-465. [15] Hanna J, Hubel A, Lemke E. Diffusion-based extraction of DMSO from a cell suspension in a three stream, vertical microchannel [J]. Biotechnology and Bioengineering, 2012, 109(9): 2316-2324. [16] 杨云, 周新丽, 戴建军, 等. 微流控线性加载低温保护剂减少猪MⅡ期卵母细胞的渗透损伤 [J]. 生物化学与生物物理进展, 2016, 43(6): 616-623. [17] Heo YS, Lee HJ, Hassell BA, et al. Controlled loading of cryoprotectants (CPAs) to oocyte with linear and complex CPA profiles on a microfluidic platform [J]. Lab on a Chip, 2011, 11(20): 3530-3537. [18] Sahu PK, Golia A, Sen AK. Analytical, numerical and experimental investigations of mixing fluids in microchannel [J]. Microsystem Technologies, 2012, 18(6): 823-832. [19] 张绍志, 王葳, 陈光明. 低温保护剂加入/去除过程中细胞体积的极值 [J]. 生物数学学报, 2004, 19(4): 465-471. [20] Mullen SF, Rosenbaum M, Critser JK. The effect of osmotic stress on the cell volume, metaphase II spindle and developmental potential of in vitro matured porcine oocytes [J]. Cryobiology, 2007, 54(3): 281-289. [21] Wang Liang, Liu Jun, Zhou Guanbin, et al. Quantitative investigations on the effects of exposure durations to thecombined cryoprotective agents on mouse oocyte vitrification procedures [J]. Biology of Reproduction, 2011, 85(5): 884-894. [22] Wang Xin, Al-Naib A, Sun Dawen, et al. Membrane permeability characteristics of bovine oocytes and development of a step-wise cryoprotectant adding and diluting protocol [J]. Cryobiology, 2010, 61(1): 58-65. [23] Song YS, Moon S, Hulli L, et al. Microfluidics for cryopreservation [J]. Lab on a Chip, 2009, 9(13): 1874-1881. |
|
|
|