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在海鞘卵细胞质和皮层重组过程中,在后植物皮层观察到的微管阵列。

Microtubule array observed in the posterior-vegetal cortex during cytoplasmic and cortical reorganization of the ascidian egg.

作者信息

Ishii Hirokazu, Goto Toshiyuki, Nishikata Takahito

机构信息

Frontiers of Innovative Research in Science and Technology (FIRST), Konan University, Kobe, Hyogo, 650-0047, Japan.

出版信息

Dev Growth Differ. 2017 Oct;59(8):648-656. doi: 10.1111/dgd.12405. Epub 2017 Oct 2.

Abstract

Body axis formation during embryogenesis results from asymmetric localization of maternal factors in the egg. Shortly before the first cleavage in ascidian eggs, cell polarity along the anteroposterior (A-P) axis is established and the cytoplasmic domain (myoplasm) relocates from the vegetal to the posterior region in a microtubule-dependent manner. Through immunostaining, tubulin accumulation during this reorganization is observable on the myoplasm cortex. However, more detailed morphological features of microtubules remain relatively unknown. In this study, we invented a new reagent that improves the immunostaining of cortical microtubules and successfully visualized a parallel array of thick microtubules. During reorganization, they covered nearly the entire myoplasm cortical region, beneath the posterior-vegetal cortex. We designated this microtubule array as CAMP (cortical array of microtubules in posterior vegetal region). During the late phase of reorganization, CAMP shrank and the myoplasm formed a crescent-like cytoplasmic domain. When the CAMP formation was inhibited by sodium azide, myoplasmic reorganization and A-P axis formation were both abolished, suggesting that CAMP is important for these two processes.

摘要

胚胎发育过程中的体轴形成源于卵子中母体因子的不对称定位。在海鞘卵第一次分裂前不久,沿前后(A-P)轴的细胞极性得以确立,细胞质区域(肌质)以微管依赖的方式从植物极迁移至后部区域。通过免疫染色,在此重组过程中微管蛋白在肌质皮层上的积累是可观察到的。然而,微管更详细的形态特征仍相对未知。在本研究中,我们发明了一种新试剂,它改善了皮层微管的免疫染色,并成功地使一组平行排列的粗微管可视化。在重组过程中,它们几乎覆盖了整个肌质皮层区域,位于植物极后部皮层之下。我们将这种微管阵列命名为CAMP(植物极后部区域的皮层微管阵列)。在重组后期,CAMP收缩,肌质形成新月形的细胞质区域。当CAMP的形成被叠氮化钠抑制时,肌质重组和A-P轴形成均被消除,这表明CAMP对这两个过程很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7cf/11520962/55df0681d436/DGD-59-648-g005.jpg

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