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精子发生和附睾成熟过程中质膜脂质双层结构的变化。

Changes in the organization of the lipid bilayer of the plasma membrane during spermatogenesis and epididymal maturation.

作者信息

Schlegel R A, Hammerstedt R, Cofer G P, Kozarsky K, Freidus D, Williamson P

出版信息

Biol Reprod. 1986 Mar;34(2):379-91. doi: 10.1095/biolreprod34.2.379.

Abstract

Ram, bull, and mouse sperm cells were stained with several fluorescent membrane probes. In contrast to nonspecific probes, merocyanine 540 (MC540), which displays preferential binding to loosely packed phospholipids in model membranes, was specifically localized to the anterior portion of the head and the midpiece of mature sperm. To establish when during development this distinctive staining pattern was acquired, germ cells from prepubescent and adult mouse testes as well as sperm from the caput, corpus, and cauda epididymides were isolated and examined. Localized staining with MC540 was not observed until sperm reached the corpus epididymidis, where those cells with a completely translocated (i.e., distally located) cytoplasmic droplet fluoresced. Likewise, when sperm were stained with fluoresceinated concanavalin A (fl-ConA), a localized pattern of fluorescence with lectin restricted to the anterior portion of the head was not observed until the corpus epididymidis was reached. However, in contrast to MC540 staining, only a fraction of sperm with completely translocated droplets exhibited this localized staining with fl-ConA, the remainder exhibiting diffuse fluorescence over the entire cell as seen on caput epididymal sperm. These developmental changes in staining patterns are specific to murine cells, since no change in the pattern of staining by either MC540 or fl-ConA was seen on epididymal sperm of the ram. These results are discussed with respect to: 1) species-to-species differences in sperm membrane features; and 2) the hypothesis that domains of loosely packed lipids may be involved in the regionalization of membrane proteins that occurs during sperm development.

摘要

用几种荧光膜探针分别对公羊、公牛和小鼠的精子细胞进行染色。与非特异性探针不同,部花青540(MC540)能优先结合模型膜中排列疏松的磷脂,它特异性定位于成熟精子头部的前部和中段。为确定在发育过程中的何时获得这种独特的染色模式,分别分离并检测了青春期前和成年小鼠睾丸中的生殖细胞以及附睾头、附睾体和附睾尾的精子。直到精子到达附睾体时才观察到MC540的定位染色,此时那些细胞质滴完全移位(即位于远端)的细胞发出荧光。同样,当用荧光素标记的伴刀豆球蛋白A(fl-ConA)对精子进行染色时,直到到达附睾体才观察到凝集素荧光的定位模式,且该模式仅限于头部的前部。然而,与MC540染色不同,只有一部分细胞质滴完全移位的精子表现出这种fl-ConA定位染色,其余精子则如附睾头精子那样在整个细胞上呈现弥漫性荧光。染色模式的这些发育变化是小鼠细胞特有的,因为在公羊的附睾精子上未观察到MC540或fl-ConA染色模式的变化。针对以下方面对这些结果进行了讨论:1)精子膜特征的种间差异;2)排列疏松的脂质结构域可能参与精子发育过程中膜蛋白区域化的假说。

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