Iomini C, Justine J L
Laboratoire de Biologie Parasitaire, Protistologie, Helminthologie, Muséum National d'Histoire Naturelle, Paris, France.
Tissue Cell. 1997 Feb;29(1):107-18. doi: 10.1016/s0040-8166(97)80077-8.
Spermiogenesis and the spermatozoon of Echinostoma caproni (from experimentally infested laboratory mice) were investigated by several methods. Transmission electron microscopy shows that spermiogenesis consists of proximo-distal fusion of three processes followed by elongation of the spermatid. Scanning electron microscopy shows that the spermatozoon is a filiform cell, 235 microns in length, with a cylindrical anterior extremity and a broader posterior extremity. Epifluorescence microscopy, including immunocytochemistry of tubulin and labelling of nucleus with specific dyes, has provided valuable additional information. Migration of the nuclei from the common cytoplasmic mass of spermatids to the distal part of the elongating spermatids is visualized, and centrioles demonstrated in the proximal, anterior region, and the nucleus in the distal, posterior region of the spermatozoon. One axoneme has a distal extremity which in the mature spermatozoon extends 30 microns more distally than the other, with the result that the posterior part of the spermatozoon contains a single axoneme and nucleus. Immunocytochemistry experiments show that a region, 15 microns in length, not labelled by the anti-tubulin antibodies with certain fixation-permeabilization procedures, corresponds to a region which, by transmission electron microscopy, shows external ornamentation on the membrane. This region has a bilaterally asymmetric pattern (in TEM), forms angles or coils according to the fixation used, and marks the boundary between two distinct patterns of movement. Spermiogenesis and the spermatozoon in E. caproni correspond to the general pattern found in the digeneans, with the exception of this asymmetric region. It is emphasized that the use of various methods provides a better understanding of sperm structure than transmission electron microscopy alone, particularly in the case of long, filiform spermatozoa.
通过多种方法对卡氏棘口吸虫(来自实验感染的实验室小鼠)的精子发生和精子进行了研究。透射电子显微镜显示,精子发生包括三个过程的近远融合,随后是精子细胞的伸长。扫描电子显微镜显示,精子是一种丝状细胞,长235微米,前端呈圆柱形,后端较宽。落射荧光显微镜,包括微管蛋白的免疫细胞化学和用特定染料标记细胞核,提供了有价值的额外信息。可以观察到细胞核从精子细胞的共同细胞质团向伸长的精子细胞远端迁移,并在精子近端前部区域显示出中心粒,在精子远端后部区域显示出细胞核。一条轴丝的远端在成熟精子中比另一条轴丝更向远端延伸30微米,结果精子的后部包含一条轴丝和一个细胞核。免疫细胞化学实验表明,在某些固定通透程序下,一个15微米长的区域未被抗微管蛋白抗体标记,该区域在透射电子显微镜下显示膜上有外部装饰。该区域具有双侧不对称模式(在透射电子显微镜下),根据所用固定方法形成角度或卷曲,并标志着两种不同运动模式之间的边界。卡氏棘口吸虫的精子发生和精子与复殖吸虫的一般模式相符,但该不对称区域除外。需要强调的是,与单独使用透射电子显微镜相比,使用多种方法能更好地理解精子结构,特别是对于长丝状精子的情况。