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老年男性的生精小管退化

Seminiferous tubule involution in elderly men.

作者信息

Paniagua R, Nistal M, Amat P, Rodriguez M C, Martin A

出版信息

Biol Reprod. 1987 May;36(4):939-47. doi: 10.1095/biolreprod36.4.939.

Abstract

The observation of different types of seminiferous tubules (from tubules with normal spermatogenesis to sclerosed tubules) in aging human testes points to the progressive stages of tubular involution in elderly men. The tubules with hypospermatogonesis (reduced number of elongated spermatids) show numerous morphological anomalies in the germ cells, including multinucleated cells. Abnormal germ cells degenerate, causing Steroli cell vacuolation. These vacuoles correspond to dilations of the extracellular spaces resulting from the premature exfoliation of germ cells. Degenerating cells that are phagocytized by Sertoli cells lead to an accumulation of lipid droplets in the Sertoli cell cytoplasm. The loss of germ cells begins with spermatids, but progressively affects the preceding germ cell types, and tubules with maturation arrested at the level of spermatocytes or spermatogonia are observed. Simultaneously, an enlargement of the tunica propria occurs. This leads to the formation of sclerosed tubules, some of which display a low seminiferous epithelium consisting of a few cells--including lipid-loaded Sertoli cells and both Ap and Ad spermatogonia--and others, showing complete sclerosis, are devoid of seminiferous epithelium. The development of tubular involution is similar to that reported after experimental ischemia, which also seems to cause nonspecific effects on the testis such as multinucleate cells, vacuoles, and increased lipids in Sertoli cells.

摘要

对老年男性睾丸中不同类型生精小管(从具有正常精子发生的小管到硬化小管)的观察表明,老年男性的小管退化存在渐进阶段。精子发生减少(长形精子细胞数量减少)的小管中,生殖细胞存在大量形态异常,包括多核细胞。异常生殖细胞退化,导致支持细胞空泡化。这些空泡对应于生殖细胞过早脱落引起的细胞外间隙扩张。被支持细胞吞噬的退化细胞导致支持细胞胞质中脂滴积累。生殖细胞的丢失始于精子细胞,但逐渐影响之前的生殖细胞类型,并且观察到精子发生在精母细胞或精原细胞水平停滞的小管。同时,固有膜会增大。这导致硬化小管的形成,其中一些小管的生精上皮由少数细胞组成,包括充满脂质的支持细胞以及Ap和Ad精原细胞,而其他一些显示完全硬化的小管则没有生精上皮。小管退化的发展与实验性缺血后报道的情况相似,实验性缺血似乎也会对睾丸产生非特异性影响,如多核细胞、空泡以及支持细胞中脂质增加。

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