首页> 外文期刊>Brain Structure and Function >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
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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

机译:成年人类睾丸支持细胞的有丝分裂活性:一项免疫组织化学研究,用于表征显示睾丸发育不全综合征的患者睾丸中的支持细胞

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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-α, 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.
机译:在青春期期间,由于功能活跃的成年Sertoli细胞中未成熟的Sertoli前细胞的分化,正常的体细胞Sertoli细胞会发生剧烈的形态变化。睾丸支持细胞的成熟伴随着精子发生之前的有丝分裂活性的丧失,青春期前的丧失以及成人免疫组化的睾丸支持细胞分化标志物的出现。不育成年患者的睾丸通常表现出许多睾丸发育不全综合征(TDS)的组织学迹象,例如微石块,仅支持细胞(SCO)的小管,含有原位癌的小管和生精小管(Sertoli细胞结节)。然而,支持细胞瘤是非常罕见的肿瘤,这可能是由于基于支持细胞肿瘤发生的肿瘤性支持细胞的机制和时间起源仍然未知。为了阐明成年TDS患者和未成熟的Sertoli细胞瘤中未成熟的曲细精管中Sertoli细胞分化的状态,我们比较了Sertoli细胞分化标志物波形蛋白,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与增生的SCO小管的抗原,雄激素受体和连接蛋白43有关。另外,我们首次证明了通过成年人类睾丸支持细胞细胞节中的Ki67和PC​​NA免疫染色,存在增殖的支持细胞。我们的数据表明,Sertoli细胞结节中有丝分裂活跃的Sertoli细胞将在青春期之前被捕,与教条相反,它不代表胎儿或新生儿细胞。由于Sertoli细胞结节中的所有标记均显示出与赘生性Sertoli细胞相同的染色模式,但与具有增生作用的SCO小管的Sertoli细胞中的染色模式不同,因此可以推测成年男性的Sertoli细胞肿瘤可能起源于Sertoli细胞结节。

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