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公牛和公猪精子质膜冷诱导的超微结构变化

Cold-induced ultrastructural changes in bull and boar sperm plasma membranes.

作者信息

De Leeuw F E, Chen H C, Colenbrander B, Verkleij A J

机构信息

Department of Molecular Cell Biology, University of Utrecht, The Netherlands.

出版信息

Cryobiology. 1990 Apr;27(2):171-83. doi: 10.1016/0011-2240(90)90009-s.

Abstract

The effect of low temperatures on the ultrastructure of the plasma membrane of bull and boar spermatozoa was investigated. Cold-induced changes in the organization of sperm plasma membrane components were demonstrated by the use of fast-freezing combined with freeze-fracture electron microscopy. This preparation technique ensures fixation without artifacts. At 38 degrees C bull and boar spermatozoa exhibited a random distribution of intramembranous particles over the plasma membrane of both head and tail. Exposure to 0 degree C resulted in redistribution of the intramembranous particles: on the head and principal piece of bull spermatozoa and on the principal piece of boar spermatozoa, particle-free areas were observed, whereas on the boar sperm head, particle aggregates were present. The original particle distribution was restored upon rewarming of bull and boar spermatozoa to 38 degrees C, as well as after freezing and thawing of bull spermatozoa. Dilution of bull and boar semen into Tris-dilution buffer and Beltsville Thaw Solution-dilution buffer, respectively, could not prevent cold-induced redistribution of intramembranous particles. The observed particle reorganization upon cooling was interpreted as the result of lateral phase separation in the plasma membrane. Species-dependent differences in cold-induced ultrastructural changes were considered to be determined by lipid composition and asymmetry of the plasma membrane, and might be related to differences in cold resistance between species.

摘要

研究了低温对公牛和公猪精子质膜超微结构的影响。通过快速冷冻结合冷冻蚀刻电子显微镜技术,证实了精子质膜成分组织的冷诱导变化。这种制备技术可确保固定时无假象。在38℃时,公牛和公猪精子的膜内颗粒在头部和尾部的质膜上呈随机分布。暴露于0℃会导致膜内颗粒重新分布:在公牛精子的头部和主段以及公猪精子的主段上,观察到无颗粒区域,而在公猪精子头部则存在颗粒聚集。公牛和公猪精子重新升温至38℃时,以及公牛精子冷冻和解冻后,颗粒的原始分布得以恢复。将公牛和公猪精液分别稀释到Tris稀释缓冲液和贝尔茨维尔解冻溶液稀释缓冲液中,无法防止冷诱导的膜内颗粒重新分布。冷却时观察到的颗粒重组被解释为质膜横向相分离的结果。冷诱导超微结构变化的物种依赖性差异被认为是由质膜的脂质组成和不对称性决定的,并且可能与物种间抗寒能力的差异有关。

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