Mechanisms of Development of Sperm Defects.

4区 生物学 Q3 Medicine
Albert Barth, Viv E A Perry, Lauren E Hamilton, Peter Sutovsky, Richard Oko
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引用次数: 0

Abstract

The intention of this chapter is to provide insights on the possible causes and disruptive mechanisms in play of some commonly occurring bull sperm abnormalities. Consideration is given to mutations of genes, inhibition of enzymes, deficiencies of trace elements, toxins, simulated stress, hormonal changes, hypoosmolarity and cold shock that cause similar disruptive phenotypes in development and structure seen in commonly occurring bull sperm abnormalities. The possible causes and disruptive mechanisms of the following bull sperm defects, arising from the above research, are evaluated: Tail stump, Decapitations, Dag, Dag-like, Short tail, Pseudodoplet, Segmental aplasia of the mitochondrial sheath, Coiled tails, Knobbed and Nuclear vacuolation. In addition, the idea arising from murid research, that mutations affecting sperm head shape most always affect motility, while mutations affecting sperm tail formation rarely affect sperm head shape is considered. Examples of mutations in genes or inhibition of enzymes involved with the early stages of acrosome formation are given that lead to a variety of 'globozoospermic-like' sperm head phenotypes all of which are associated with various degrees of aberrant sperm tail morphologies.

精子缺陷的发育机制。
本章的目的是提供一些常见的公牛精子异常的可能原因和破坏性机制的见解。考虑到基因突变、酶抑制、微量元素缺乏、毒素、模拟应激、激素变化、低渗和冷休克,这些因素在常见的公牛精子异常中导致类似的发育和结构破坏性表型。对上述研究引起的下述雄性精子缺陷的可能原因和破坏机制进行了评估:残尾、断头、Dag、Dag样、短尾、假小点、线粒体鞘节段性发育不全、盘尾、结节状和核空泡化。此外,还考虑了murid研究中提出的观点,即影响精子头形的突变通常会影响精子的运动能力,而影响精子尾部形成的突变很少影响精子头形。本文给出了与顶体形成早期阶段有关的基因突变或酶抑制的例子,这些突变或酶抑制导致各种“类球形精子”精子头部表型,所有这些表型都与不同程度的异常精子尾部形态相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.00
自引率
0.00%
发文量
0
期刊介绍: "Advances in Anatomy, Embryology and Cell Biology" presents critical reviews on all topical fields of normal and experimental anatomy including cell biology. The multi-perspective presentation of morphological aspects of basic biological phenomen in the human constitutes the main focus of the series. The contributions re-evaluate the latest findings and show ways for further research.
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