成人睾丸中支持细胞的有丝分裂活性:一项免疫组织化学研究,以表征睾丸发育不良综合征患者睾丸索中的支持细胞。

Anatomy and Embryology Pub Date : 2006-06-01 Epub Date: 2006-01-21 DOI:10.1007/s00429-005-0075-8
Ralph Brehm, Rodolfo Rey, Sabine Kliesch, Klaus Steger, Alexander Marks, Martin Bergmann
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引用次数: 43

摘要

在青春期,正常的体细胞支持细胞由于未成熟的前支持细胞向功能活跃的成年支持细胞分化而发生了巨大的形态变化。支持细胞成熟伴随着精子发生前有丝分裂活性的丧失,青春期前和成年免疫组织化学支持细胞分化标志物的丧失。成年不育患者的睾丸通常表现出许多睾丸发育不良综合征(TDS)的组织学征象,如微石、仅支持细胞(SCO)小管、含有原位癌的小管和未成熟的精小管(支持细胞结节)。然而,支持细胞肿瘤是一种非常罕见的肿瘤,这可能是由于支持细胞肿瘤发生的机制和时间起源尚不清楚。为了明确成人TDS和支持细胞瘤患者未成熟精小管中支持细胞的分化状态,我们比较了支持细胞分化标志物vimentin、抑制素- α、抗muellerian激素、细胞角蛋白18、m2a抗原、雄激素受体和连接蛋白43的表达与增生SCO小管的表达。此外,我们首次通过Ki67-和pcna -免疫染色证实了成人睾丸支持细胞结节中存在增殖的支持细胞。我们的数据表明,支持细胞结节中的有丝分裂活跃的支持细胞在青春期之前会被阻止,与教条相反,不代表胎儿或新生儿细胞。由于支持细胞结节的所有标记物显示的染色模式与肿瘤性支持细胞相同,但与SCO小管增生的支持细胞不同,因此可以推测成年男性的支持细胞肿瘤可能起源于支持细胞结节。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mitotic activity of Sertoli cells in adult human testis: an immunohistochemical study to characterize Sertoli cells in testicular cords from patients showing testicular dysgenesis syndrome.

During puberty, normal somatic Sertoli cells undergo dramatic morphological changes due to the differentiation of immature pre-Sertoli cells in functionally active adult Sertoli cells. Sertoli cell maturation is accompanied with loss of their mitotic activity before onset of spermatogenesis and loss of pre-pubertal and occurrence of adult immunohistochemical Sertoli cell differentiation markers. Testes of infertile adult patients often exhibit numerous histological signs of testicular dysgenesis syndrome (TDS) such as microliths, Sertoli cell only (SCO) tubules, tubules containing carcinoma in situ and immature seminiferous tubules (Sertoli cell nodules). Sertoli cell tumours, however, are very rare neoplasms possibly due to the fact that the mechanism and temporal origin of neoplastic Sertoli cells underlying Sertoli cell tumourigenesis still remain unknown. To clarify the state of Sertoli cell differentiation in both immature seminiferous tubules of adult patients with TDS and Sertoli cell tumour, we compared the expression of the Sertoli cell differentiation markers vimentin, inhibin-alpha, anti-Muellerian-hormone, cytokeratin 18, M2A-antigen, androgen receptor and connexin43 with that of SCO tubules with hyperplasia. In addition, we demonstrated for the first time the existence of proliferating Sertoli cells by Ki67- and PCNA-immunostaining in Sertoli cell nodules of the adult human testis. Our data indicate that mitotically active Sertoli cells in Sertoli cell nodules will be arrested prior to puberty and, contrary to dogma, do not represent foetal or neonatal cells. Since all markers in Sertoli cell nodules revealed a staining pattern identical to that in neoplastic Sertoli cells, but different to that in Sertoli cells of SCO tubules with hyperplasia, it may be speculated that Sertoli cell tumours in adult men may originate from Sertoli cell nodules.

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