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果蝇 ESCRT-III 复合物蛋白 VPS24 的遗传分析揭示了其在溶酶体动态平衡中的新功能。

Genetic analysis of the Drosophila ESCRT-III complex protein, VPS24, reveals a novel function in lysosome homeostasis.

机构信息

Department of Biology and Center for Cellular Dynamics, The Pennsylvania State University, University Park, PA, United States of America.

出版信息

PLoS One. 2021 May 6;16(5):e0251184. doi: 10.1371/journal.pone.0251184. eCollection 2021.

Abstract

The ESCRT pathway is evolutionarily conserved across eukaryotes and plays key roles in a variety of membrane remodeling processes. A new Drosophila mutant recovered in our forward genetic screens for synaptic transmission mutants mapped to the vps24 gene encoding a subunit of the ESCRT-III complex. Molecular characterization indicated a loss of VPS24 function, however the mutant is viable and thus loss of VPS24 may be studied in a developed multicellular organism. The mutant exhibits deficits in locomotion and lifespan and, notably, these phenotypes are rescued by neuronal expression of wild-type VPS24. At the cellular level, neuronal and muscle cells exhibit marked expansion of a ubiquitin-positive lysosomal compartment, as well as accumulation of autophagic intermediates, and these phenotypes are rescued cell-autonomously. Moreover, VPS24 expression in glia suppressed the mutant phenotype in muscle, indicating a cell-nonautonomous function for VPS24 in protective intercellular signaling. Ultrastructural analysis of neurons and muscle indicated marked accumulation of the lysosomal compartment in the vps24 mutant. In the neuronal cell body, this included characteristic lysosomal structures associated with an expansive membrane compartment with a striking tubular network morphology. These findings further define the in vivo roles of VPS24 and the ESCRT pathway in lysosome homeostasis and their potential contributions to neurodegenerative diseases characterized by defective ESCRT or lysosome function.

摘要

ESCRT 途径在真核生物中是进化保守的,在各种膜重塑过程中发挥关键作用。我们在突触传递突变体的正向遗传学筛选中回收的一个新的果蝇突变体被映射到编码 ESCRT-III 复合物亚基的 vps24 基因上。分子特征表明 VPS24 功能丧失,但该突变体是存活的,因此可以在发育中的多细胞生物中研究 VPS24 的缺失。该突变体表现出运动和寿命缺陷,值得注意的是,这些表型可以通过神经元表达野生型 VPS24 来挽救。在细胞水平上,神经元和肌肉细胞表现出泛素阳性溶酶体区室的明显扩张,以及自噬中间产物的积累,这些表型可以自主挽救。此外,VPS24 在神经胶质细胞中的表达抑制了肌肉中的突变表型,表明 VPS24 在保护性细胞间信号传递中具有非自主细胞功能。对神经元和肌肉的超微结构分析表明,vps24 突变体中溶酶体区室的明显积累。在神经元细胞体中,这包括与具有显著管状网络形态的扩张膜区室相关的特征性溶酶体结构。这些发现进一步定义了 VPS24 和 ESCRT 途径在溶酶体动态平衡中的体内作用及其在以 ESCRT 或溶酶体功能缺陷为特征的神经退行性疾病中的潜在贡献。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f82d/8101729/1f8d4b67d359/pone.0251184.g001.jpg

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