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大鼠减数分裂前期和精子发生过程中的核仁结构与合成活性

Nucleolar structure and synthetic activity during meiotic prophase and spermiogenesis in the rat.

作者信息

Schultz M C, Leblond C P

机构信息

Department of Anatomy, McGill University, Montreal, Quebec, Canada.

出版信息

Am J Anat. 1990 Sep;189(1):1-10. doi: 10.1002/aja.1001890102.

Abstract

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.

摘要

借助连续切片,对发育中的大鼠精母细胞和精子细胞的核仁超微结构进行了研究。此外,在睾丸内注射3H(5')-尿苷1小时后处死的大鼠中检测核仁的放射自显影反应,并将其作为核糖体RNA(rRNA)合成速率的指标。从细线前期到偶线期的初级精母细胞有小核仁,通常由纤维中心、纤维成分和颗粒成分组成,其内部有狭窄的间隙。在粗线期早期和中期,核仁增大到初始大小的约九倍,纤维成分和颗粒成分形成广泛的索状网络——核仁线——其内部有宽阔的间隙。同时,出现了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件。最后,从粗线期后期到第一次成熟分裂,核仁发生浓缩,表现为纤维中心收缩成小团块,而纤维成分和颗粒成分浓缩并相互分离,间隙逐渐减小。在次级精母细胞中,核仁紧密且相当小,而在年轻精子细胞中它们也紧密且更小。核仁在伸长的精子细胞中消失。在3H-尿苷放射自显影片中,年轻初级精母细胞中的核仁标记较弱,在粗线期早期逐渐增加,在粗线期中期结束时较强,但在粗线期后期直至第一次成熟分裂期间逐渐减少。在次级精母细胞和精子细胞中,没有明显的核仁标记。总之,年轻精母细胞中核仁的rRNA合成较低。在粗线期,当核仁增大并形成花边状的核仁线时,rRNA合成逐渐增加,在粗线期中期结束时达到高水平。然而,在从粗线期后期开始的核仁成分的浓缩和分离过程中,合成逐渐减少并消失。由第二次成熟分裂产生的小而紧密的精子细胞不合成rRNA。

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