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“圆头”精子缺陷。超微结构与减数分裂分离研究。

'Round head' sperm defect. Ultrastructural and meiotic segregation study.

作者信息

Moretti E, Collodel G, Scapigliati G, Cosci I, Sartini B, Baccetti B

机构信息

Department of Pediatrics, Obstetrics and Reproductive Medicine, Biology Section, University of Siena, Regional Referral Center for Male Infertility, Siena University General Hospital, Italy.

出版信息

J Submicrosc Cytol Pathol. 2005 Nov;37(3-4):297-303.

Abstract

The sperm 'round head' defect, also known as globozoospermia, is an uncommon alteration of sperm morphology generally characterised by 100% round headed sperm totally lacking an acrosome. This alteration is a genetic sperm defect as demonstrated by analysing the incidence of these alterations in a population of infertile men showing a history of consanguinity and cases belonging to the same family. Ultrastructural characteristics and meiotic segregation in spermatozoa from two patients affected by 'round head' sperm defect were investigated. The sperm quality was examined by light and transmission electron microscopy (TEM) and fluorescence in situ hybridization (FISH) analysis was performed in order to investigate the meiotic behavior of chromosomes namely gonosomes and chromosome 18. TEM analysis, mathematically elaborated, clearly diagnosed the 'round head' genetic sperm defect and highlighted at the same time the presence of other phenotypic alterations belonging to pathologies such as immaturity, apoptosis and necrosis. It is possible to hypothesize that round headed sperm could be a 'weak phenotype' allowing the sperm pathologies to overlap with a sperm defect of genetic origin, further compromising fertilizing potential. FISH analysis revealed a positive correlation between globozoospermia and higher disomies of sex chromosomes and diploidies suggesting a higher risk of creating an aneuploid embryo after intracytoplasmic sperm injection.

摘要

精子“圆头”缺陷,也称为球状精子症,是一种罕见的精子形态改变,其一般特征为100%的圆头精子,完全缺乏顶体。通过分析不育男性群体中这种改变的发生率(这些男性有近亲结婚史以及属于同一家族的病例),证明这种改变是一种遗传性精子缺陷。对两名患有“圆头”精子缺陷的患者的精子进行了超微结构特征和减数分裂分离研究。通过光学显微镜和透射电子显微镜(TEM)检查精子质量,并进行荧光原位杂交(FISH)分析,以研究染色体(即性染色体和18号染色体)的减数分裂行为。经数学处理的TEM分析明确诊断出“圆头”遗传性精子缺陷,同时突出显示了属于诸如不成熟、凋亡和坏死等病理状态的其他表型改变。可以推测,圆头精子可能是一种“弱表型”,使得精子病理状态与遗传性精子缺陷重叠,进一步损害受精潜力。FISH分析显示球状精子症与性染色体更高的二体性和二倍体性之间存在正相关,这表明在胞浆内单精子注射后产生非整倍体胚胎的风险更高。

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