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微管和肌动蛋白细胞骨架动力学在. 的雄性减数分裂细胞中

Microtubule and Actin Cytoskeletal Dynamics in Male Meiotic Cells of .

机构信息

Istituto di Biologia e Patologia Molecolari del CNR, c/o Dipartimento di Biologia e Biotecnologie, Sapienza Università di Roma, Piazzale A. Moro 5, 00185 Roma, Italy.

出版信息

Cells. 2022 Feb 16;11(4):695. doi: 10.3390/cells11040695.

Abstract

dividing spermatocytes offer a highly suitable cell system in which to investigate the coordinated reorganization of microtubule and actin cytoskeleton systems during cell division of animal cells. Like male germ cells of mammals, spermatogonia and spermatocytes undergo cleavage furrow ingression during cytokinesis, but abscission does not take place. Thus, clusters of primary and secondary spermatocytes undergo meiotic divisions in synchrony, resulting in cysts of 32 secondary spermatocytes and then 64 spermatids connected by specialized structures called ring canals. The meiotic spindles in males are substantially larger than the spindles of mammalian somatic cells and exhibit prominent central spindles and contractile rings during cytokinesis. These characteristics make male meiotic cells particularly amenable to immunofluorescence and live imaging analysis of the spindle microtubules and the actomyosin apparatus during meiotic divisions. Moreover, because the spindle assembly checkpoint is not robust in spermatocytes, male meiosis allows investigating of whether gene products required for chromosome segregation play additional roles during cytokinesis. Here, we will review how the research studies on male meiotic cells have contributed to our knowledge of the conserved molecular pathways that regulate spindle microtubules and cytokinesis with important implications for the comprehension of cancer and other diseases.

摘要

精母细胞提供了一个高度合适的细胞系统,可用于研究动物细胞有丝分裂过程中微管和肌动蛋白细胞骨架系统的协调重排。与哺乳动物的雄性生殖细胞一样,精原细胞和精母细胞在胞质分裂过程中经历分裂沟内陷,但不会发生胞质分离。因此,初级和次级精母细胞簇同步进行减数分裂,导致 32 个次级精母细胞和 64 个通过称为环管的特殊结构连接的精细胞形成。雄性减数分裂纺锤体明显大于哺乳动物体细胞的纺锤体,在胞质分裂过程中表现出明显的中央纺锤体和收缩环。这些特征使得雄性减数分裂细胞特别适合于免疫荧光和活细胞成像分析减数分裂过程中的纺锤体微管和肌动球蛋白装置。此外,由于精母细胞中的纺锤体组装检查点不健全,雄性减数分裂可以研究染色体分离所需的基因产物在胞质分裂过程中是否发挥额外的作用。在这里,我们将回顾关于雄性减数分裂细胞的研究如何促进我们对调节纺锤体微管和胞质分裂的保守分子途径的认识,这对理解癌症和其他疾病具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3857/8870657/47ceb53cee8a/cells-11-00695-g001.jpg

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