大鼠减数分裂前期和精子发生核仁结构和合成活性。

M C Schultz, C P Leblond
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引用次数: 20

摘要

用连续切片法观察了发育中的大鼠精母细胞和精母细胞核仁的超微结构。此外,在大鼠睾丸内注射3H(5’)-尿苷1小时后,观察核仁的放射自显影反应,并以此作为核糖体RNA (rRNA)合成速度的指标。从preleptotene到zygotene的原代精母细胞具有小的核仁,核仁通常由纤维中心、纤维成分和颗粒成分组成,其中有狭窄的间隙。在粗成期早期和中期,核仁增大到初始大小的9倍左右,原纤维和颗粒成分形成了一个广泛的索状网络——核仁小体,其中有广阔的间隙。同时,出现与颗粒成分相同但与核仁不同的结构;它们被称为核仁外颗粒元素。最后,从粗成期晚期到第一次成熟分裂,核仁发生凝结,表现为原纤维中心收缩成小团块,同时原纤维和颗粒成分相互凝聚分离,间隙逐渐减少。在次级精母细胞中,核仁致密且相当小,而在年轻精子细胞中,核仁也致密且更小。核仁在伸长的精子中消失。在3h -尿苷放射显像中,核仁标记在年轻的初级精母细胞中较弱,在粗成期早期逐渐增加,在粗成期中期结束时较强,但在粗成期晚期直至第一次成熟分裂时逐渐减弱。在次级精母细胞和精母细胞中,没有明显的核仁标记。综上所述,在年轻的精母细胞中,核仁的rRNA合成较低。在粗期中期,随着核仁扩大并形成花边核仁瘤,rRNA合成在粗期中期结束时逐渐增加到高水平。然而,从粗成期晚期开始,在核仁组分的凝聚和分离过程中,合成逐渐减少并消失。由第二次成熟分裂产生的小而致密的精子不合成rRNA。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Nucleolar structure and synthetic activity during meiotic prophase and spermiogenesis in the rat.

The ultrastructure of nucleoli was examined in developing rat spermatocytes and spermatids, with the help of serial sections. In addition, the radioautographic reaction of nucleoli as examined in rats sacrificed 1 hr after intratesticular injection of 3H(5')-uridine and taken as an index of the rate of synthesis of ribosomal RNA (rRNA). Primary spermatocytes from preleptotene to zygotene have small nucleoli typically composed of fibrillar centers, a fibrillar component, and a granular component, within which are narrow interstitial spaces. During early and mid-pachytene, nucleoli enlarge to about nine times their initial size, with the fibrillar and granular components forming an extensive network of cords--a nucleolonema--within which are wide interstitial spaces. Meanwhile, there appear structures identical to the granular component but distinct from nucleoli; they are referred to as extranucleolar granular elements. Finally, from late pachytene to the first maturation division, nucleoli undergo condensation, as shown by contraction of fibrillar centers into small clumps, while fibrillar and granular components condense and segregate from each other, with a gradual decrease in interstitial spaces. In secondary spermatocytes, nucleoli are compact and rather small, while in young spermatids they are also compact and even smaller. Nucleoli disappear in elongating spermatids. In 3H-uridine radioautographs, nucleolar label is weak in young primary spermatocytes, increases progressively during early pachytene, is strong by the end of mid pachytene, but gradually decreases during late pachytene up to the first maturation division. In secondary spermatocytes and spermatids, there is no significant nucleolar label. In conclusion, rRNA synthesis by nucleoli is low in young spermatocytes. During pachytene, while nucleoli enlarge and form a lacy nucleolonema, rRNA synthesis increases gradually to a high level by the end of mid pachytene. However, during the condensation and segregation of nucleolar components occurring from late pachytene onward, the synthesis gradually decreases and disappears. The small, compact spermatids arising from the second maturation division do not synthesize rRNA.

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