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MYO10 促进哺乳动卵泡发生过程中跨带投射依赖的生殖细胞-体细胞接触。

MYO10 promotes transzonal projection-dependent germ line-somatic contact during mammalian folliculogenesis†.

机构信息

Department of Obstetrics and Gynecology, McGill University, Montreal, Canada.

Research Institute of the McGill University Health Center, Montreal, Canada.

出版信息

Biol Reprod. 2022 Aug 9;107(2):474-487. doi: 10.1093/biolre/ioac078.

Abstract

Granulosa cells of growing ovarian follicles elaborate filopodia-like structures termed transzonal projections (TZPs) that supply the enclosed oocyte with factors essential for its development. Little is known, however, of the mechanisms underlying the generation of TZPs. We show in mouse and human that filopodia, defined by an actin backbone, emerge from granulosa cells in early stage primary follicles and that actin-rich TZPs become detectable as soon as a space corresponding to the zona pellucida appears. mRNA encoding Myosin10 (MYO10), a motor protein that accumulates at the base and tips of filopodia and has been implicated in their initiation and elongation, is present in granulosa cells and oocytes of growing follicles. MYO10 protein accumulates in foci located mainly between the oocyte and innermost layer of granulosa cells, where it colocalizes with actin. In both mouse and human, the number of MYO10 foci increases as oocytes grow, corresponding to the increase in the number of actin-TZPs. RNAi-mediated depletion of MYO10 in cultured mouse granulosa cell-oocyte complexes is associated with a 52% reduction in the number of MYO10 foci and a 28% reduction in the number of actin-TZPs. Moreover, incubation of cumulus-oocyte complexes in the presence of epidermal growth factor, which triggers a 93% reduction in the number of actin-TZPs, is associated with a 55% reduction in the number of MYO10 foci. These results suggest that granulosa cells possess an ability to elaborate filopodia, which when directed toward the oocyte become actin-TZPs, and that MYO10 increases the efficiency of formation or maintenance of actin-TZPs.

摘要

生长中的卵巢卵泡的颗粒细胞产生称为透明带间突(TZPs)的类似丝状伪足的结构,为被包裹的卵母细胞提供发育所需的关键因子。然而,对于 TZPs 形成的机制知之甚少。我们在小鼠和人中显示,由肌动蛋白骨架定义的丝状伪足从早期初级卵泡的颗粒细胞中出现,并且一旦出现与透明带相对应的空间,富含肌动蛋白的 TZPs 就变得可检测到。编码肌球蛋白 10(MYO10)的 mRNA 存在于生长中的卵泡的颗粒细胞和卵母细胞中,MYO10 是一种运动蛋白,在丝状伪足的基部和尖端积累,并被牵连到它们的起始和延伸。MYO10 蛋白在主要位于卵母细胞和最内层颗粒细胞之间的焦点中积累,在那里它与肌动蛋白共定位。在小鼠和人中,随着卵母细胞的生长,MYO10 焦点的数量增加,与肌动蛋白-TZPs 的数量增加相对应。在培养的小鼠颗粒细胞-卵母细胞复合物中用 RNAi 介导的 MYO10 耗竭与 MYO10 焦点数量减少 52%和肌动蛋白-TZPs 数量减少 28%相关。此外,在表皮生长因子存在下孵育卵丘-卵母细胞复合物,表皮生长因子触发肌动蛋白-TZPs 的数量减少 93%,与 MYO10 焦点数量减少 55%相关。这些结果表明,颗粒细胞具有产生丝状伪足的能力,当这些丝状伪足指向卵母细胞时,就变成了肌动蛋白-TZPs,而 MYO10 增加了肌动蛋白-TZPs 的形成或维持效率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d228/9382396/84578d4e2f7d/ioac078ga.jpg

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