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精子发生:探索精子激活分子基础的优秀模型。

Spermiogenesis in : An Excellent Model to Explore the Molecular Basis for Sperm Activation.

机构信息

Department of Life Science, Faculty of Science and Engineering, Setsunan University, Osaka 572-8508, Japan.

出版信息

Biomolecules. 2023 Apr 7;13(4):657. doi: 10.3390/biom13040657.

Abstract

spermiogenesis converts non-motile spermatids into motile, fertilization-competent spermatozoa. Two major events include the building of a pseudopod required for motility and fusion of membranous organelles (MOs)-intracellular secretory vesicles-with the spermatid plasma membrane required for the proper distribution of sperm molecules in mature spermatozoa. The mouse sperm acrosome reaction-a sperm activation event occurring during capacitation-is similar to MO fusion in terms of cytological features and biological significance. Moreover, and mouse , both encoding members of the ferlin family, are indispensable for MO fusion and acrosome reaction, respectively. Genetics-based studies have identified many genes involved in spermiogenesis pathways; however, it is unclear whether mouse orthologs of these genes are involved in the acrosome reaction. One significant advantage of using for studying sperm activation is the availability of in vitro spermiogenesis, which enables combining pharmacology and genetics for the assay. If certain drugs can activate both and mouse spermatozoa, these drugs would be useful probes to explore the mechanism underlying sperm activation in these two species. By analyzing mutants whose spermatids are insensitive to the drugs, genes functionally relevant to the drugs' effects can be identified.

摘要

精子发生将非运动的精母细胞转化为运动的、有受精能力的精子。两个主要事件包括建立一个伪足,这是运动所必需的,以及融合膜细胞器(MOs)-细胞内分泌小泡-与精子质膜,这是成熟精子中精子分子适当分布所必需的。鼠精子顶体反应-在获能期间发生的精子激活事件-在细胞学特征和生物学意义上与 MO 融合相似。此外, 和 ,分别编码 ferlin 家族的成员,对于 MO 融合和顶体反应是不可或缺的。基于遗传学的研究已经确定了许多参与精子发生途径的 基因;然而,尚不清楚这些基因的鼠同源物是否参与顶体反应。使用 来研究精子激活的一个重要优势是体外精子发生的可用性,这使得药理学和遗传学可以结合用于检测。如果某些药物可以激活 和鼠精子,这些药物将是探索这两种物种精子激活机制的有用探针。通过分析对药物不敏感的 突变体,可以鉴定与药物作用相关的功能基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e243/10136096/83aacbe6c349/biomolecules-13-00657-g001.jpg

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