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中段异常延长、主段水平缺乏轴丝和外周致密纤维、微管数量过多:一种可能源于遗传的精子缺陷?

Abnormal elongation of midpiece, absence of axoneme and outer dense fibers at principal piece level, supernumerary microtubules: a sperm defect of possible genetic origin?

作者信息

Moretti Elena, Pascarelli Nicola Antonio, Federico Maria Grazia, Renieri Tommaso, Collodel Giulia

机构信息

Department of Surgery, Biology Section, University of Siena, Interdepartmental Centre for Research and Therapy of Male Infertility, Siena, Italy.

出版信息

Fertil Steril. 2008 Oct;90(4):1201.e3-8. doi: 10.1016/j.fertnstert.2007.11.050. Epub 2008 Feb 21.

Abstract

OBJECTIVE

To characterize a flagellar defect involving 95% of the sperm population from an infertile man.

DESIGN

Case report.

SETTING

Interdepartmental Centre for Research and Therapy of Male Infertility, Siena, Italy.

PATIENT(S): A 42-year-old infertile man with severe asthenozoospermia.

INTERVENTION(S): Family history, physical examination, hormonal analysis, microbial assays, semen analysis, transmission electron microscopy (TEM) and scanning electron microscopy (SEM), tubulin distribution investigated by immunocytochemistry, fluorescence in situ hybridization for chromosomes 18, X, and Y.

MAIN OUTCOME MEASURE(S): Ultrastructural abnormalities of the flagellum detected by methods listed.

RESULT(S): Ultrastructural analysis revealed, in 95% of sperm cells, the total absence of the axoneme and outer dense fibers at the principal piece level, whereas the midpiece appeared abnormally long. Tubulin localization showed a total disorganization of the axoneme with a network of microtubular structures emerging randomly at any level of the flagellum. Fluorescence in situ hybridization analysis was normal.

CONCLUSION(S): We report a rare sperm tail defect, characterized by abnormal elongation of the midpiece and absence of the axoneme and the outer dense fibers at the principal piece level in 95% of flagella. This defect occurs in the vast majority of the sperm population from a sterile man, and therefore a genetic origin could be hypothesized.

摘要

目的

对一名不育男性中95%的精子群体所存在的鞭毛缺陷进行特征描述。

设计

病例报告。

地点

意大利锡耶纳男性不育研究与治疗跨部门中心。

患者

一名42岁患有严重弱精子症的不育男性。

干预措施

家族史、体格检查、激素分析、微生物检测、精液分析、透射电子显微镜检查(TEM)和扫描电子显微镜检查(SEM)、通过免疫细胞化学研究微管蛋白分布、对18号染色体、X染色体和Y染色体进行荧光原位杂交。

主要观察指标

通过所列方法检测到的鞭毛超微结构异常。

结果

超微结构分析显示,95%的精子细胞在主段水平完全缺失轴丝和外周致密纤维,而中段显得异常长。微管蛋白定位显示轴丝完全紊乱,在鞭毛的任何水平都有随机出现的微管结构网络。荧光原位杂交分析正常。

结论

我们报告了一种罕见的精子尾部缺陷,其特征为中段异常延长,且95%的鞭毛在主段水平缺失轴丝和外周致密纤维。这种缺陷发生在一名不育男性的绝大多数精子群体中,因此可以推测其起源于遗传。

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