钙在多泡内溶酶体中的储存。

IF 2 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Cameron C Scott, Vaibhav Wasnik, Paula Nunes-Hassler, Nicolas Demaurex, Karsten Kruse, Jean Gruenberg
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引用次数: 0

摘要

现在已经确定,内溶酶体,也称为晚期内体,除了内质网外,还充当细胞内钙储备。虽然丰富的钙结合蛋白为后一个隔室提供了钙储存能力,但基本上对内溶酶体中钙储存的机制一无所知。在本文中,我们提出内溶酶体膜的结构组织驱动了隔室的钙储存能力。事实上,内溶酶体表现出特征性的多泡超微结构,管腔内膜提供了大量额外的双层表面。我们使用一种理论方法来研究内泌体的钙储存能力,使用已知的双层钙结合亲和力和内溶酶体膜组织的形态学数据。最后,我们在SNX3耗竭后通过实验测试了我们的预测,以降低管腔内膜含量。我们得出的结论是,内溶酶体的主要负电荷脂质和蛋白质在哺乳动物细胞的酸性钙储存中充当钙结合分子,而管腔内膜的大表面积提供了必要的储存能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Calcium storage in multivesicular endo-lysosome.

It is now established that endo-lysosomes, also referred to as late endosomes, serve as intracellular calcium store, in addition to the endoplasmic reticulum. While abundant calcium-binding proteins provide the latter compartment with its calcium storage capacity, essentially nothing is known about the mechanism responsible for calcium storage in endo-lysosomes. In this paper, we propose that the structural organization of endo-lysosomal membranes drives the calcium storage capacity of the compartment. Indeed, endo-lysosomes exhibit a characteristic multivesicular ultrastructure, with intralumenal membranes providing a large amount of additional bilayer surface. We used a theoretical approach to investigate the calcium storage capacity of endosomes, using known calcium binding affinities for bilayers and morphological data on endo-lysosome membrane organization. Finally, we tested our predictions experimentally after Sorting Nexin 3 depletion to decrease the intralumenal membrane content. We conclude that the major negatively-charge lipids and proteins of endo-lysosomes serve as calcium-binding molecules in the acidic calcium stores of mammalian cells, while the large surface area of intralumenal membranes provide the necessary storage capacity.

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来源期刊
Physical biology
Physical biology 生物-生物物理
CiteScore
4.20
自引率
0.00%
发文量
50
审稿时长
3 months
期刊介绍: Physical Biology publishes articles in the broad interdisciplinary field bridging biology with the physical sciences and engineering. This journal focuses on research in which quantitative approaches – experimental, theoretical and modeling – lead to new insights into biological systems at all scales of space and time, and all levels of organizational complexity. Physical Biology accepts contributions from a wide range of biological sub-fields, including topics such as: molecular biophysics, including single molecule studies, protein-protein and protein-DNA interactions subcellular structures, organelle dynamics, membranes, protein assemblies, chromosome structure intracellular processes, e.g. cytoskeleton dynamics, cellular transport, cell division systems biology, e.g. signaling, gene regulation and metabolic networks cells and their microenvironment, e.g. cell mechanics and motility, chemotaxis, extracellular matrix, biofilms cell-material interactions, e.g. biointerfaces, electrical stimulation and sensing, endocytosis cell-cell interactions, cell aggregates, organoids, tissues and organs developmental dynamics, including pattern formation and morphogenesis physical and evolutionary aspects of disease, e.g. cancer progression, amyloid formation neuronal systems, including information processing by networks, memory and learning population dynamics, ecology, and evolution collective action and emergence of collective phenomena.
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