• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

鞭毛支架的重排会在受精过程中诱导精子停止运动。

Reorganization of the flagellum scaffolding induces a sperm standstill during fertilization.

机构信息

Instituto de Biología y Medicina Experimental, Consejo Nacional de Investigaciones Científicas y Técnicas (IBYME-CONICET), Buenos Aires, Argentina.

Departamento de Genética del Desarrollo y Fisiología Molecular, Instituto de Biotecnología, Universidad Nacional Autónoma de México, Morelos, Mexico.

出版信息

Elife. 2024 Nov 13;13:RP93792. doi: 10.7554/eLife.93792.

DOI:10.7554/eLife.93792
PMID:39535529
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11560130/
Abstract

Mammalian sperm delve into the female reproductive tract to fertilize the female gamete. The available information about how sperm regulate their motility during the final journey to the fertilization site is extremely limited. In this work, we investigated the structural and functional changes in the sperm flagellum after acrosomal exocytosis (AE) and during the interaction with the eggs. The evidence demonstrates that the double helix actin network surrounding the mitochondrial sheath of the midpiece undergoes structural changes prior to the motility cessation. This structural modification is accompanied by a decrease in diameter of the midpiece and is driven by intracellular calcium changes that occur concomitant with a reorganization of the actin helicoidal cortex. Midpiece contraction occurs in a subset of cells that undergo AE, and live-cell imaging during in vitro fertilization showed that the midpiece contraction is required for motility cessation after fusion is initiated. These findings provide the first evidence of the F-actin network's role in regulating sperm motility, adapting its function to meet specific cellular requirements during fertilization, and highlighting the broader significance of understanding sperm motility.

摘要

哺乳动物精子深入女性生殖道以受精女性配子。关于精子在向受精部位的最后旅程中如何调节其运动的可用信息极其有限。在这项工作中,我们研究了顶体反应后和与卵子相互作用期间精子鞭毛的结构和功能变化。有证据表明,中段线粒体鞘周围的双螺旋肌动蛋白网络在运动停止前发生结构变化。这种结构修饰伴随着中段直径的减小,并由与肌动蛋白螺旋皮质重排同时发生的细胞内钙变化驱动。中段收缩发生在经历顶体反应的细胞亚群中,体外受精的活细胞成像显示,中段收缩是融合启动后运动停止所必需的。这些发现为 F-actin 网络在调节精子运动中的作用提供了第一个证据,使其适应受精过程中特定细胞的需求,突出了理解精子运动的更广泛意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/2682c08a8086/elife-93792-sa3-fig12.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/0919e078d8a1/elife-93792-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/df1312032341/elife-93792-fig1-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/f5b82ff83e2d/elife-93792-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/264c3a76586d/elife-93792-fig2-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/2ab0e506fd1e/elife-93792-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/ebe1ed1ebfdf/elife-93792-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/bfaacaf212a4/elife-93792-fig4-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/217dcc16638a/elife-93792-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/01e9af4ea9ef/elife-93792-fig5-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/3fded6fc6119/elife-93792-fig5-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/ff724881bbe8/elife-93792-fig5-figsupp3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/8c8ae458bf99/elife-93792-fig5-figsupp4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/3819d966bdf8/elife-93792-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/b997d96d2db4/elife-93792-fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/6d12a67c1eae/elife-93792-fig7-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/a5c4d42eb46a/elife-93792-fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/609781fc980e/elife-93792-fig9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/9291bbc2a285/elife-93792-sa3-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/c81fb213aa27/elife-93792-sa3-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/8aafcd43a61e/elife-93792-sa3-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/8743e4e2fc31/elife-93792-sa3-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/31bc7610ac87/elife-93792-sa3-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/5a4f6a42d63c/elife-93792-sa3-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/c27ceffb58d0/elife-93792-sa3-fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/01b187b3f280/elife-93792-sa3-fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/426ee53d0118/elife-93792-sa3-fig9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/63d565e14474/elife-93792-sa3-fig10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/c78b186351da/elife-93792-sa3-fig11.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/2682c08a8086/elife-93792-sa3-fig12.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/0919e078d8a1/elife-93792-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/df1312032341/elife-93792-fig1-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/f5b82ff83e2d/elife-93792-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/264c3a76586d/elife-93792-fig2-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/2ab0e506fd1e/elife-93792-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/ebe1ed1ebfdf/elife-93792-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/bfaacaf212a4/elife-93792-fig4-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/217dcc16638a/elife-93792-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/01e9af4ea9ef/elife-93792-fig5-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/3fded6fc6119/elife-93792-fig5-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/ff724881bbe8/elife-93792-fig5-figsupp3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/8c8ae458bf99/elife-93792-fig5-figsupp4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/3819d966bdf8/elife-93792-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/b997d96d2db4/elife-93792-fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/6d12a67c1eae/elife-93792-fig7-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/a5c4d42eb46a/elife-93792-fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/609781fc980e/elife-93792-fig9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/9291bbc2a285/elife-93792-sa3-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/c81fb213aa27/elife-93792-sa3-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/8aafcd43a61e/elife-93792-sa3-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/8743e4e2fc31/elife-93792-sa3-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/31bc7610ac87/elife-93792-sa3-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/5a4f6a42d63c/elife-93792-sa3-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/c27ceffb58d0/elife-93792-sa3-fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/01b187b3f280/elife-93792-sa3-fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/426ee53d0118/elife-93792-sa3-fig9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/63d565e14474/elife-93792-sa3-fig10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/c78b186351da/elife-93792-sa3-fig11.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdd/11560130/2682c08a8086/elife-93792-sa3-fig12.jpg

相似文献

1
Reorganization of the flagellum scaffolding induces a sperm standstill during fertilization.鞭毛支架的重排会在受精过程中诱导精子停止运动。
Elife. 2024 Nov 13;13:RP93792. doi: 10.7554/eLife.93792.
2
Reorganization of the Flagellum Scaffolding Induces a Sperm Standstill During Fertilization.鞭毛支架的重组在受精过程中导致精子静止。
bioRxiv. 2024 Jul 2:2023.06.22.546073. doi: 10.1101/2023.06.22.546073.
3
Heads or tails? Structural events and molecular mechanisms that promote mammalian sperm acrosomal exocytosis and motility.头还是尾?促进哺乳动物精子顶体反应和运动的结构事件和分子机制。
Mol Reprod Dev. 2012 Jan;79(1):4-18. doi: 10.1002/mrd.21393. Epub 2011 Oct 26.
4
The actin cytoskeleton of the mouse sperm flagellum is organized in a helical structure.小鼠精子鞭毛的肌动蛋白细胞骨架呈螺旋状排列。
J Cell Sci. 2018 Jun 11;131(11):jcs215897. doi: 10.1242/jcs.215897.
5
During capacitation in bull spermatozoa, actin and PLC-ζ undergo dynamic interactions.在公牛精子获能过程中,肌动蛋白和磷脂酶Cζ发生动态相互作用。
Zygote. 2017 Oct;25(5):558-566. doi: 10.1017/S0967199417000260. Epub 2017 Sep 20.
6
Sperm chemotaxis and regulation of flagellar movement by Ca2+.精子的趋化性和钙离子对鞭毛运动的调节。
Mol Hum Reprod. 2011 Aug;17(8):457-65. doi: 10.1093/molehr/gar041. Epub 2011 May 24.
7
Importance of sperm morphology during sperm transport and fertilization in mammals.精子形态在哺乳动物精子运输和受精过程中的重要性。
Asian J Androl. 2016 Nov-Dec;18(6):844-850. doi: 10.4103/1008-682X.186880.
8
How do sperm swim? Molecular mechanisms underlying sperm motility.精子是如何游动的?精子运动的分子机制。
Cell Mol Biol (Noisy-le-grand). 2003 May;49(3):357-69.
9
Functional deficiencies and a reduced response to calcium in the flagellum of mouse sperm lacking SPAG16L.缺乏 SPAG16L 的小鼠精子鞭毛功能缺陷且对钙的反应降低。
Biol Reprod. 2010 Apr;82(4):736-44. doi: 10.1095/biolreprod.109.080143. Epub 2009 Dec 30.
10
Comparative analysis of mammalian sperm ultrastructure reveals relationships between sperm morphology, mitochondrial functions and motility.哺乳动物精子超微结构的比较分析揭示了精子形态、线粒体功能和运动能力之间的关系。
Reprod Biol Endocrinol. 2019 Aug 15;17(1):66. doi: 10.1186/s12958-019-0510-y.

引用本文的文献

1
Dynamic relocation of PKA regulatory subunits during sperm capacitation: Linking PKA to the CatSper signaling complex.精子获能过程中蛋白激酶A调节亚基的动态重新定位:将蛋白激酶A与精子阳离子通道CatSper信号复合体相联系
Proc Natl Acad Sci U S A. 2025 Jun 10;122(23):e2501741122. doi: 10.1073/pnas.2501741122. Epub 2025 Jun 6.

本文引用的文献

1
Extending resolution within a single imaging frame.在单个成像帧内扩展分辨率。
Nat Commun. 2022 Dec 2;13(1):7452. doi: 10.1038/s41467-022-34693-9.
2
A genetically targeted sensor reveals spatial and temporal dynamics of acrosomal calcium and sperm acrosome exocytosis.一种基因靶向传感器揭示了顶体钙的时空动态和精子顶体胞吐作用。
J Biol Chem. 2022 May;298(5):101868. doi: 10.1016/j.jbc.2022.101868. Epub 2022 Mar 27.
3
The cell biology of fertilization: Gamete attachment and fusion.受精的细胞生物学:配子附着与融合。
J Cell Biol. 2021 Oct 4;220(10). doi: 10.1083/jcb.202102146. Epub 2021 Aug 30.
4
The Fertilization Enigma: How Sperm and Egg Fuse.受精之谜:精子与卵子如何融合。
Annu Rev Cell Dev Biol. 2021 Oct 6;37:391-414. doi: 10.1146/annurev-cellbio-120219-021751. Epub 2021 Jul 21.
5
Cdc42 localized in the CatSper signaling complex regulates cAMP-dependent pathways in mouse sperm.定位于精子阳离子通道(CatSper)信号复合物中的Cdc42调节小鼠精子中依赖环磷酸腺苷(cAMP)的信号通路。
FASEB J. 2021 Aug;35(8):e21723. doi: 10.1096/fj.202002773RR.
6
Long-term segmentation-free assessment of head-flagellum movement and intracellular calcium in swimming human sperm.长期无分割评估游动人体精子的头鞭毛运动和细胞内钙离子。
J Cell Sci. 2021 Feb 11;134(3):jcs250654. doi: 10.1242/jcs.250654.
7
Sperm proteins SOF1, TMEM95, and SPACA6 are required for sperm-oocyte fusion in mice.精子蛋白 SOF1、TMEM95 和 SPACA6 对于小鼠精卵融合是必需的。
Proc Natl Acad Sci U S A. 2020 May 26;117(21):11493-11502. doi: 10.1073/pnas.1922650117. Epub 2020 May 11.
8
Fast and accurate sCMOS noise correction for fluorescence microscopy.快速准确的 sCMOS 荧光显微镜噪声校正。
Nat Commun. 2020 Jan 3;11(1):94. doi: 10.1038/s41467-019-13841-8.
9
Actin polymerization is activated by terahertz irradiation.肌动蛋白聚合被太赫兹辐射激活。
Sci Rep. 2018 Jul 3;8(1):9990. doi: 10.1038/s41598-018-28245-9.
10
SRRF: Universal live-cell super-resolution microscopy.SRRF:通用活细胞超分辨率显微镜。
Int J Biochem Cell Biol. 2018 Aug;101:74-79. doi: 10.1016/j.biocel.2018.05.014. Epub 2018 May 28.