Watson P F, Kunze E, Cramer P, Hammerstedt R H
Department of Molecular and Cell Biology, Pennsylvania State University, University Park.
J Androl. 1992 Mar-Apr;13(2):131-8.
Measurements were made of critical osmolality, the osmolality at which 50% of the cells are lysed, and of the permeation time, the time taken to lyse 50% of the cells in an osmotic solution lower than the critical osmolality, for fowl and bull spermatozoa. Cell lysis was determined by means of fluorescent viability stains (carboxyfluorescein diacetate and propidium iodide) using a flow cytometer. The advantages and pitfalls of this approach are addressed. The values obtained have been used to compute the water permeability, or hydraulic conductivity, of the plasma membrane and its activation energy for each species. Fowl spermatozoa were found to have a lower critical osmolality (17 mOsm) than bull spermatozoa (36 mOsm), and this is discussed in relation to the differences in cell shape and size. The hydraulic conductivities of fowl and bull spermatozoa were 2.1 and 10.8 microns x atmosphere x minute, respectively, and the respective activation energies were 4.4 and 3.0 kcal/mol. The relevance of these findings to cryopreservation of spermatozoa is considered.
对家禽和公牛精子的临界渗透压(即50%的细胞发生裂解时的渗透压)以及渗透时间(即在低于临界渗透压的渗透溶液中50%的细胞发生裂解所需的时间)进行了测量。使用流式细胞仪,通过荧光活力染色剂(羧基荧光素二乙酸酯和碘化丙啶)来确定细胞裂解情况。探讨了这种方法的优点和缺陷。所获得的值已用于计算每种物种质膜的水渗透性或水力传导率及其活化能。发现家禽精子的临界渗透压(17毫渗量)低于公牛精子(36毫渗量),并结合细胞形状和大小的差异对此进行了讨论。家禽和公牛精子的水力传导率分别为2.1和10.8微米×大气压×分钟,各自的活化能分别为4.4和3.0千卡/摩尔。考虑了这些发现与精子冷冻保存的相关性。