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Ultrastructural analysis of five patients with total sperm immotility

机译:五例总精子运动力超微结构分析

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Asthenozoospermia has been related to structural defects of the sperm flagellum. However, few reports have studied in detail the ultrastructure of sperm with total immotility. We present an ultrastructural study of sperm from five patients with total sperm immotility, four due to dysplasia of the fibrous sheath (DFS) and one with situs-inversus. Of the four patients with DFS, three cases presented a hypertrophic and hyperplastic fibrous sheath that invaded the midpiece space, absence of the annulus, and a short midpiece containing a few disorganized and pale mitochondria. Of these cases, two presented absence of the central complex and radial spokes; another additionally presented absence of dynein arms and nexin bridges; and the other patient presented an intact annulus with a dysplastic fibrous sheath restricted to the principal piece with disorganized microtubule doublets. The patient with situs-inversus presented severe respiratory symptoms, with absence of dynein arms and nexin bridges. In conclusion, we present three cases with DFS associated with total sperm immotility, abnormal mitochondria, and absence of the annulus, central pair complex and radial spokes, of which one had in addition absence of dynein arms and nexin bridges. We also describe a patient, with total sperm immotility and a different presentation of DFS, as the annulus was present and the dysplastic fibrous sheath was restricted to the principal piece. These findings thus confirm the heterogeneity of the DFS condition. The changes observed in the patient with situs-inversus also further support previous observations.
机译:弱精子症与精子鞭毛的结构缺陷有关。但是,很少有报道详细研究具有完全运动能力的精子超微结构。我们目前对五名具有全部精子活动力的患者进行精子超微结构研究,其中四名由于纤维鞘(DFS)发育异常而一名患有仰卧位。在4例DFS患者中,有3例出现了肥厚性增生性纤维鞘,侵袭了中膜间隙,无瓣环,中膜较短,其中包含一些杂乱无章的苍白线粒体。在这些情况中,有两个没有中央辐条和径向辐条。另一个另外表现出缺乏动力蛋白臂和神经毒素桥;另一名患者表现为完整的瓣环,发育不良的纤维鞘被限制在主要部分,并伴有微管双联体紊乱。眼睑内翻的患者表现出严重的呼吸道症状,无动力肽和神经桥蛋白。总之,我们发现了3例DFS,与总精子运动力,线粒体异常,环空,中枢对复合体和radial骨辐不相关,其中1例还缺少动力蛋白臂和神经桥。我们还描述了一个患者,该患者具有完全的精子运动能力和不同的DFS表现,因为存在瓣环并且发育不良的纤维鞘被限制在主要部分。因此,这些发现证实了DFS条件的异质性。眼睑内翻患者观察到的变化也进一步支持以前的观察。

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