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半融合体与相互作用的蛋白脂质纳米液滴:一种新型细胞器复合体的形成

Hemifusomes and Interacting Proteolipid Nanodroplets: Formation of a Novel Cellular Organelle Complex.

作者信息

Tavakoli Amirrasoul, Hu Shiqiong, Ebrahim Seham, Kachar Bechara

出版信息

bioRxiv. 2024 Aug 29:2024.08.28.610112. doi: 10.1101/2024.08.28.610112.

DOI:10.1101/2024.08.28.610112
PMID:39253452
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11383319/
Abstract

Within cells, vesicle fusion, scission, and the formation of intraluminal vesicles are critical processes that facilitate traffic, degradation, and recycling of cellular components, and maintenance of cellular homeostasis. Despite significant advancements in elucidating the molecular mechanisms that drive these dynamic processes, the direct in situ visualization of membrane remodeling intermediates remains challenging. Here, through the application of cryo-electron tomography in mammalian cells, we have identified a previously undescribed vesicular organelle complex with unique membrane topology: heterotypic hemifused vesicles that share extended hemifusion diaphragms (HDs) with a 42 nm proteolipid nanodroplet (PND) at their rim. We have termed these organelle complexes "hemifusomes". The HDs of hemifusomes exhibit a range of sizes and curvatures, including the formation of lens-shaped compartments encapsulated within the membrane bilayer. The morphological diversity of the lens-shaped vesicle aligns with a step-wise process of their intraluminal budding, ultimately leading to their scission and the generation of intraluminal vesicles. We propose that hemifusomes function as versatile platforms for protein and lipid sorting and as central hubs for the biogenesis of intraluminal vesicles and the formation of multivesicular bodies.

摘要

在细胞内,囊泡融合、分裂以及腔内囊泡的形成是促进细胞成分运输、降解和循环以及维持细胞内稳态的关键过程。尽管在阐明驱动这些动态过程的分子机制方面取得了重大进展,但膜重塑中间体的直接原位可视化仍然具有挑战性。在这里,通过在哺乳动物细胞中应用冷冻电子断层扫描技术,我们发现了一种以前未描述过的具有独特膜拓扑结构的囊泡细胞器复合体:异型半融合囊泡,其边缘与一个42纳米的蛋白脂质纳米液滴(PND)共享延伸的半融合隔膜(HDs)。我们将这些细胞器复合体称为“半融合体”。半融合体的HDs呈现出一系列大小和曲率,包括形成包裹在膜双层内的透镜状隔室。透镜状囊泡的形态多样性与其腔内出芽的逐步过程相一致,最终导致其分裂并产生腔内囊泡。我们提出,半融合体作为蛋白质和脂质分选的通用平台,以及作为腔内囊泡生物发生和多泡体形成的中心枢纽发挥作用。

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