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单殖吸虫精子发生的比较超微结构研究。1. 巨杯吸虫属(单后盘吸虫纲杯叶科)

[Comparative ultrastructural study of spermiogenesis in Monogenea. 1. Megalocotyle (Monopisthocotylea Capsalidae)].

作者信息

Justine J L, Mattei X

出版信息

J Ultrastruct Res. 1983 Mar;82(3):296-308. doi: 10.1016/s0022-5320(83)80016-1.

Abstract

In Megalocotyle the zones of differentiation (ZD) are short and incomplete; there is no median cytoplasmic process or free flagella. Some peripheral microtubules are present in early ZD, but they disappear. Each nucleus of the common cytoplasmic mass inserts one extremity into a ZD. The mitochondria fuse around this extremity and form a beadlike perforated sphere. Later this sphere slides along the nucleus away from the plasmic membrane like a bead on a string. Each mitochondrial bead (MB), as it moves, trails part of its bulk in the form of a solid streamer; two parallel centrioles follow the MB, each generating a trailing 9 + "1" flagellum. The result is a four-part ensemble extending from each MB to each ZD: the two axonemes, the streamer, and the nucleus, with no membrane separating it from the surrounding cytoplasm. Subsequently a cytoplasmic canal (CC) is formed. The arching membranes, originally located at the base of the ZD, migrate along the four-part ensembles as far as the MB, leaving behind two membranes which define the CC. This formation of the CC is remarkable in that it occurs after migration of the centrioles. At the end of spermiogenesis, the cytoplasmic mass reveals 64 parallel CC each containing an immature spermatozoid whose free rear extremity lengthens out. Each spermatozoid is then detached at its anterior extremity set in the cytoplasmic mass. As in most monopisthocotylean monogeneans, the mature spermatozoid of Megalocotyle lacks peripheral microtubules, although its early ZD has microtubules which subsequently disappear. This feature distinguishes it from trematodes and polyopisthocotylean monogeneans, whose mature spermatozoid keep their ZD microtubules.

摘要

在巨杯吸虫中,分化区(ZD)短且不完整;没有中央细胞质突起或游离鞭毛。在早期分化区存在一些外周微管,但它们会消失。共同细胞质团中的每个细胞核将一个末端插入一个分化区。线粒体围绕这个末端融合并形成一个珠状穿孔球体。之后,这个球体沿着细胞核从质膜滑开,就像串在绳子上的珠子。每个线粒体珠(MB)移动时,会以实心拖尾的形式拖曳其部分主体;两个平行的中心粒跟随线粒体珠,每个中心粒产生一条拖尾的9 + “1”鞭毛。结果是一个从每个线粒体珠延伸到每个分化区的四部分组合:两条轴丝、拖尾和细胞核,没有膜将其与周围细胞质分隔开。随后形成一条细胞质管(CC)。最初位于分化区基部的拱形膜沿着四部分组合迁移到线粒体珠处,留下界定细胞质管的两层膜。细胞质管的这种形成很显著,因为它发生在中心粒迁移之后。在精子发生结束时,细胞质团显示出64条平行的细胞质管,每条都包含一个未成熟的精子,其游离的后端会伸长。然后每个精子在位于细胞质团中的前端处分离。与大多数单殖吸虫纲单殖亚纲动物一样,巨杯吸虫的成熟精子缺乏外周微管,尽管其早期分化区有微管,这些微管随后会消失。这一特征使其与吸虫和多后盘吸虫纲单殖亚纲动物区分开来,它们的成熟精子保留其分化区微管。

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