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首页> 外文期刊>Cell and Tissue Research >Adhesion between plasma membrane and mitochondria with linking filaments in relation to migration of cytoplasmic droplet during epididymal maturation in guinea pig spermatozoa.
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Adhesion between plasma membrane and mitochondria with linking filaments in relation to migration of cytoplasmic droplet during epididymal maturation in guinea pig spermatozoa.

机译:豚鼠精子附睾成熟过程中质膜与线粒体之间的附着力与连接细丝的迁移有关。

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High-resolution microscopy has been used to investigate the mechanism of the migration of cytoplasmic droplets during epididymal maturation of guinea pig spermatozoa. On testicular spermatozoa, droplets are located at the neck and, after passage through the middle cauda epididymidis, migrate only as far as the center of the midpiece. Initially, the space between the plasma membrane and outer mitochondrial membranes outside the droplet is 30.8+/-11.0 nm, whereas on mature spermatozoa, it significantly (P<0.01) narrows to a more consistent 15.9+/-1.3 nm. This is accompanied by the appearance of thin filaments cross-linking the two membranes above and below the droplet. Changes also occur in the arrangement of intramembranous particles (IMPs) in the plasma membrane overlying the midpiece. At the spermatid stage, linear arrays of IMPs are absent but appear on immature spermatozoa, where they are short with an irregular orientation, in the epididymis. On mature spermatozoa, numerous parallel linear arrays are present at the region where the plasma membrane adheres to the mitochondria. The membrane adhesion process can thus be observed two-dimensionally. The initial migration of the droplet from the neck is probably attributable to diffusion, with the formation of cross-linking filaments between the two membranes in the proximal midpiece preventing any backward flow and squeezing the droplet distally until it is arrested at the central midpiece by the filaments formed in the distal midpiece. The filaments might also stabilize the flagellum against hypo-osmotic stress encountered during ejaculation and within the female tract.
机译:高分辨率显微镜已用于研究豚鼠精子附睾成熟过程中细胞质小滴迁移的机制。在睾丸的精子上,液滴位于颈部,并在穿过附睾中部马尾后仅迁移至中段的中心。最初,液滴外质膜和线粒体外膜之间的空间为30.8 +/- 11.0 nm,而在成熟的精子上,其显着(P <0.01)缩小为更一致的15.9 +/- 1.3 nm。这伴随着细丝的出现,细丝将液滴上方和下方的两个膜交联。覆盖中间件的质膜中膜内颗粒(IMP)的排列也会发生变化。在精子阶段,IMPs的线性阵列不存在,但出现在附睾中的未成熟的精子上,在那里它们短小且具有不规则的取向。在成熟的精子上,质膜附着于线粒体的区域存在许多平行的线性阵列。因此可以二维地观察膜粘附过程。液滴从颈部的初始迁移可能归因于扩散,在近端中段的两个膜之间形成交联细丝可防止任何向后流动,并向远端挤压液滴,直到液滴被中间段止住在中间段为止。远端中段形成细丝。这些细丝还可以使鞭毛稳定,以抵抗射精过程中和雌性道内遇到的低渗压力。

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