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The dynamic cytoskeleton of the developing male germ cell.发育中雄性生殖细胞的动态细胞骨架。
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Manchette-acrosome disorders during spermiogenesis and low efficiency of seminiferous tubules in hypercholesterolemic rabbit model.高胆固醇血症兔模型中精子发生过程中的顶体-顶体复合体紊乱及生精小管效率低下
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The development and evolution of actin-containing organelles during spermiogenesis of a primitive nematode.一种原始线虫精子发生过程中含肌动蛋白细胞器的发育与演化
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Comprehensive Transcriptome Analysis Reveals Sex-Specific Alternative Splicing Events in Zebrafish Gonads.综合转录组分析揭示斑马鱼性腺中的性别特异性可变剪接事件。
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本文引用的文献

1
Induction of Ran GTP drives ciliogenesis.Ran GTP 的诱导驱动纤毛发生。
Mol Biol Cell. 2011 Dec;22(23):4539-48. doi: 10.1091/mbc.E11-03-0267. Epub 2011 Oct 12.
2
PP1 forms an active complex with TLRR (lrrc67), a putative PP1 regulatory subunit, during the early stages of spermiogenesis in mice.在精子发生的早期阶段,PP1 与 TLRR(lrrc67)形成一个活跃的复合物,TLRR 是一种假定的 PP1 调节亚基。
PLoS One. 2011;6(6):e21767. doi: 10.1371/journal.pone.0021767. Epub 2011 Jun 30.
3
Myosin light chain kinases and phosphatase in mitosis and cytokinesis.有丝分裂和胞质分裂中的肌球蛋白轻链激酶和磷酸酶。
Arch Biochem Biophys. 2011 Jun 15;510(2):76-82. doi: 10.1016/j.abb.2011.03.002. Epub 2011 Mar 21.
4
GMAP210 and IFT88 are present in the spermatid golgi apparatus and participate in the development of the acrosome-acroplaxome complex, head-tail coupling apparatus and tail.GMAP210 和 IFT88 存在于精细胞的高尔基体中,并参与顶体-顶体复合体、头-尾连接装置和尾部的发育。
Dev Dyn. 2011 Mar;240(3):723-36. doi: 10.1002/dvdy.22563. Epub 2011 Feb 10.
5
The posttranslational modification of tubulin undergoes a switch from detyrosination to acetylation as epithelial cells become polarized.微管蛋白的翻译后修饰在上皮细胞极化时经历从脱酪氨酸化到乙酰化的转变。
Mol Biol Cell. 2011 Apr;22(7):1045-57. doi: 10.1091/mbc.E10-06-0519. Epub 2011 Feb 9.
6
Ciliopathies: an expanding disease spectrum.纤毛病:不断扩展的疾病谱。
Pediatr Nephrol. 2011 Jul;26(7):1039-56. doi: 10.1007/s00467-010-1731-7. Epub 2011 Jan 6.
7
KIFC1-like motor protein associates with the cephalopod manchette and participates in sperm nuclear morphogenesis in Octopus tankahkeei.KIFC1 样马达蛋白与头足类顶体环相关联,并参与短蛸精子核形态发生。
PLoS One. 2010 Dec 20;5(12):e15616. doi: 10.1371/journal.pone.0015616.
8
RANBP17 is localized to the XY body of spermatocytes and interacts with SPEM1 on the manchette of elongating spermatids.RANBP17 定位于精母细胞的 X-Y 体,与伸长精子的顶体上的 SPEM1 相互作用。
Mol Cell Endocrinol. 2011 Feb 20;333(2):134-42. doi: 10.1016/j.mce.2010.12.021. Epub 2010 Dec 22.
9
The dynactin complex maintains the integrity of metaphasic centrosomes to ensure transition to anaphase.动力蛋白激活复合物维持着有丝分裂期中心体的完整性,以确保向后期过渡。
J Biol Chem. 2011 Feb 18;286(7):5589-98. doi: 10.1074/jbc.M110.167742. Epub 2010 Dec 16.
10
PLK1 phosphorylates mitotic centromere-associated kinesin and promotes its depolymerase activity.PLK1 磷酸化有丝分裂着丝粒相关驱动蛋白并促进其解聚酶活性。
J Biol Chem. 2011 Jan 28;286(4):3033-46. doi: 10.1074/jbc.M110.165340. Epub 2010 Nov 15.

发育中雄性生殖细胞的动态细胞骨架。

The dynamic cytoskeleton of the developing male germ cell.

机构信息

Department of Anatomy and Cell Biology, Brody School of Medicine, East Carolina University, Greenville, NC 27834, USA.

出版信息

Biol Cell. 2012 May;104(5):297-305. doi: 10.1111/boc.201100102. Epub 2012 Mar 14.

DOI:10.1111/boc.201100102
PMID:22276751
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3845902/
Abstract

Mammalian spermatogenesis is characterised by dramatic cellular change to transform the non-polar spermatogonium into a highly polarised and functional spermatozoon. The acquisition of cell polarity is a requisite step for formation of viable sperm. The polarity of the spermatozoon is clearly demonstrated by the acrosome at the apical pole of the cell and the flagellum at the opposite end. Spermatogenesis consists of three basic phases: mitosis, meiosis and spermiogenesis. The final phase represents the period of greatest cellular change where cell-type specific organelles such as the acrosome and the flagellum form, the nucleus migrates to the plasma membrane and elongates, chromatin condenses and residual cytoplasm is removed. An important feature of spermatogenesis is the change in the cytoskeleton that occurs throughout this pathway. In this review, the author will provide an overview of these transformations and provide insight into possible modes of regulation of these rearrangements during spermatogenesis. Although primary focus will be given to the microtubule cytoskeleton, the importance of actin filaments to the cellular transformation of the male germ cell will also be discussed.

摘要

哺乳动物的精子发生过程以剧烈的细胞变化为特征,将非极性精原细胞转化为高度极化和功能化的精子。细胞极性的获得是形成有活力精子的必要步骤。精子的极性通过细胞顶端的顶体和另一端的鞭毛清晰地显示出来。精子发生包括三个基本阶段:有丝分裂、减数分裂和精子形成。最后一个阶段代表细胞变化最大的时期,在此期间,形成细胞类型特异性细胞器,如顶体和鞭毛,核迁移到质膜并伸长,染色质浓缩,残留细胞质被去除。精子发生的一个重要特征是整个途径中细胞骨架的变化。在这篇综述中,作者将概述这些转化,并深入了解精子发生过程中这些重排的可能调节模式。尽管主要关注微管细胞骨架,但也将讨论肌动蛋白丝对雄性生殖细胞的细胞转化的重要性。