CHMP4B有助于维持德国蜚蠊泛型卵巢中卵泡细胞的完整性。

IF 2.4 4区 生物学 Q4 CELL BIOLOGY
Nuria Farrus, José Luis Maestro, Maria-Dolors Piulachs
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引用次数: 0

摘要

背景:运输所需的内体分选复合体(ESCRT)是一种高度保守的细胞机制,对许多细胞功能至关重要,包括跨膜蛋白分选、内体运输和膜裂解。CHMP4B是ESCRT-III亚复合物的一个关键成分,在黑腹果蝇的子代卵巢中对它进行了深入研究,显示了它在维持果蝇一生的生殖器官中的重要性。然而,CHMP4B在最基底的泛能卵巢中的作用仍然难以捉摸:结果:我们利用 RNAi 技术研究了 CHMP4B 在德国扁虱卵巢中两个不同生理阶段的功能:末龄若虫卵泡细胞增殖阶段和卵黄形成成虫卵泡细胞进入多倍体和内复制阶段。在缺失 Chmp4b 的标本中,肌动蛋白纤维的分布发生了变化,出现在卵泡细胞的基极,导致过多的肌动蛋白束包围基底卵泡并改变其形状。Chmp4b 的耗竭也决定了卵泡细胞膜上肌动蛋白的积聚,导致细胞形态和大小的不同。最终,这些变化会破坏卵泡细胞间的细胞间隙(通畅性),阻碍卵黄蛋白与生长中的卵母细胞结合,导致女性不育。此外,卵泡细胞的细胞核出现异常拉长,表明核运动不完全:这些结果证明,CHMP4B 对维持细胞骨架蛋白的正常表达至关重要,这些蛋白对基础卵泡的生长和成熟以及卵黄蛋白的结合至关重要。此外,卵巢基底卵泡中肌动蛋白纤维的正确分布也是成功完成排卵和产卵的关键因素:在两个不同增殖阶段获得的总体结果表明,B. germanica卵泡上皮细胞对CHMP4B的需求与组织的增殖阶段无关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

CHMP4B contributes to maintaining the follicular cells integrity in the panoistic ovary of the cockroach Blattella germanica

CHMP4B contributes to maintaining the follicular cells integrity in the panoistic ovary of the cockroach Blattella germanica

CHMP4B contributes to maintaining the follicular cells integrity in the panoistic ovary of the cockroach Blattella germanica

Background

The Endosomal Sorting Complex Required for Transport (ESCRT) is a highly conserved cellular machinery essential for many cellular functions, including transmembrane protein sorting, endosomal trafficking, and membrane scission. CHMP4B is a key component of ESCRT-III subcomplex and has been thoroughly studied in the meroistic ovaries of Drosophila melanogaster showing its relevance in maintaining this reproductive organ during the life of the fly. However, the role of the CHMP4B in the most basal panoistic ovaries remains elusive.

Results

Using RNAi, we examined the function of CHMP4B in the ovary of Blattella germanica in two different physiological stages: in last instar nymphs, with proliferative follicular cells, and in vitellogenic adults when follicular cells enter in polyploidy and endoreplication. In Chmp4b-depleted specimens, the actin fibers change their distribution, appearing accumulated in the basal pole of the follicular cells, resulting in an excess of actin bundles that surround the basal ovarian follicle and modifying their shape. Depletion of Chmp4b also determines an actin accumulation in follicular cell membranes, resulting in different cell morphologies and sizes. In the end, these changes disrupt the opening of intercellular spaces between the follicular cells (patency) impeding the incorporation of yolk proteins to the growing oocyte and resulting in female sterility. In addition, the nuclei of follicular cells appeared unusually elongated, suggesting an incomplete karyokinesis.

Conclusions

These results proved CHMP4B essential in preserving the proper expression of cytoskeleton proteins vital for basal ovarian follicle growth and maturation and for yolk protein incorporation. Moreover, the correct distribution of actin fibers in the basal ovarian follicle emerged as a critical factor for the successful completion of ovulation and oviposition.

Significance

The overall results, obtained in two different proliferative stages, suggest that the requirement of CHMP4B in B. germanica follicular epithelium is not related to the proliferative stage of the tissue.

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来源期刊
Biology of the Cell
Biology of the Cell 生物-细胞生物学
CiteScore
5.30
自引率
0.00%
发文量
53
审稿时长
>12 weeks
期刊介绍: The journal publishes original research articles and reviews on all aspects of cellular, molecular and structural biology, developmental biology, cell physiology and evolution. It will publish articles or reviews contributing to the understanding of the elementary biochemical and biophysical principles of live matter organization from the molecular, cellular and tissues scales and organisms. This includes contributions directed towards understanding biochemical and biophysical mechanisms, structure-function relationships with respect to basic cell and tissue functions, development, development/evolution relationship, morphogenesis, stem cell biology, cell biology of disease, plant cell biology, as well as contributions directed toward understanding integrated processes at the organelles, cell and tissue levels. Contributions using approaches such as high resolution imaging, live imaging, quantitative cell biology and integrated biology; as well as those using innovative genetic and epigenetic technologies, ex-vivo tissue engineering, cellular, tissue and integrated functional analysis, and quantitative biology and modeling to demonstrate original biological principles are encouraged.
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