Agca Y, Liu J, McGrath J J, Peter A T, Critser E S, Critser J K
Cryobiology Research Institute, Herman B. Wells Center for Pediatric Research, Riley Hospital for Children, Indianapolis, Indiana 46202, USA.
Cryobiology. 1998 Jun;36(4):287-300. doi: 10.1006/cryo.1998.2088.
In this study, the hydraulic conductivity (Lp), Me2SO permeability (PMe2SO), and the reflection coefficients (sigma) and their activation energies were determined for Metaphase II (MII) mouse oocytes by exposing them to 1.5 M Me2SO at temperatures of 30, 20, 10, 3, 0, and -3 degrees C. These data were then used to calculate the intracellular concentration of Me2SO at given temperatures. Individual oocytes were immobilized using a holding pipette in 5 microliters of an isosmotic PBS solution and perfused with precooled or prewarmed 1.5 M Me2SO solutions. Oocyte images were video recorded. The cell volume changes were calculated from the measurement of the diameter of the oocytes, assuming a spherical shape. The initial volume of the oocytes in the isoosmotic solution was considered 100%, and relative changes in the volume of the oocytes after exposure to the Me2SO were plotted against time. Mean (means +/- SEM) Lp values in the presence of Me2SO were (LpMe2SO) at 30, 20, 10, 3, 0 and -3 degrees C were determined to be 1.07 +/- 0.03, 0.40 +/- 0.02, 0.18 +/- 0.01, 7.60 x 10(-2) +/- 0.60 x 10(-2), 5.29 x 10(-2) +/- 0.40 x 10(-2), and 3.69 x 10(-2) +/- 0.30 x 10(-2) microns/min/atm, respectively. The PMe2SO values were 3.69 x 10(-3) +/- 0.3 x 10(-3), 1.07 x 10(-3) +/- 0.1 x 10(-3), 2.75 x 10(-4), +/- 0.15 x 10(-4), 7.83 x 10(-5) +/- 0.50 x 10(-5), 5.24 x 10(-5) +/- 0.50 x 10(-5), and 3.69 x 10(-5) +/- 0.40 x 10(-5) cm/min, respectively. The sigma values were 0.70 +/- 0.03, 0.77 +/- 0.04, 0.81 +/- 0.06, 0.91 +/- 0.05, 0.97 +/- 0.03, and 1 +/- 0.04, respectively. The estimated activation energies (Ea) for LpMe2SO, and PMe2SO, and sigma were 16.39, 23.24, and -1.75 Kcal/mol, respectively. These data may provide the fundamental basis for the development of more optimal cryopreservation protocols for MII mouse oocytes.
在本研究中,通过将中期II(MII)小鼠卵母细胞置于30、20、10、3、0和 -3摄氏度的温度下,使其暴露于1.5 M二甲基亚砜(Me2SO)中,测定了其水力传导率(Lp)、Me2SO渗透率(PMe2SO)、反射系数(sigma)及其活化能。然后利用这些数据计算给定温度下Me2SO的细胞内浓度。使用固定吸管将单个卵母细胞固定在5微升等渗磷酸盐缓冲盐水(PBS)溶液中,并用预冷或预热的1.5 M Me2SO溶液进行灌注。对卵母细胞图像进行视频记录。假设卵母细胞为球形,根据卵母细胞直径的测量计算细胞体积变化。等渗溶液中卵母细胞的初始体积视为100%,将暴露于Me2SO后卵母细胞体积的相对变化与时间作图。在30、20、10、3、0和 -3摄氏度下,Me2SO存在时的平均(平均值±标准误)Lp值(LpMe2SO)分别测定为1.07±0.03、0.40±0.02、0.18±0.01、7.60×10⁻²±0.60×10⁻²、5.29×10⁻²±0.40×10⁻²和3.69×10⁻²±0.30×10⁻²微米/分钟/大气压。PMe2SO值分别为3.69×10⁻³±0.3×10⁻³、1.07×10⁻³±0.1×...