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脂质不对称性与膜运输:作为胞吐作用和胞吞作用调节因子的结构磷脂的跨膜分布

Lipid asymmetry and membrane trafficking: Transbilayer distribution of structural phospholipids as regulators of exocytosis and endocytosis.

作者信息

Caputo Margherita, Gubar Olga, Tóth Petra, Vitale Nicolas, Gasman Stéphane, Ory Stéphane

机构信息

Centre National de La Recherche Scientifique, Université de Strasbourg, Institut des Neurosciences Cellulaires et Intégratives, Strasbourg, France; IEO, European Institute of Oncology IRCCS, Milan, Italy.

Centre National de La Recherche Scientifique, Université de Strasbourg, Institut des Neurosciences Cellulaires et Intégratives, Strasbourg, France.

出版信息

J Biol Chem. 2025 Jul 2;301(8):110441. doi: 10.1016/j.jbc.2025.110441.

DOI:10.1016/j.jbc.2025.110441
PMID:40609796
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12329543/
Abstract

The plasma membrane of eukaryotic cells is highly dynamic and asymmetrically organized. Its continuous remodeling plays a crucial role in diverse cellular processes, including apoptosis, blood coagulation, and vesicular trafficking. The distribution and rearrangement of phospholipids (PLs) within the bilayer are tightly regulated, influencing membrane curvature, tension, and organization. This review examines the role of PL asymmetry in vesicle fusion, the final step of exocytosis, and in vesicular membrane retrieval by compensatory endocytosis in neurosecretory cells, with a particular emphasis on structural PLs such as phosphatidylcholine (PC), phosphatidylethanolamine (PE), and phosphatidylserine (PS). We discuss the molecular mechanisms that maintain and disrupt PLs asymmetry and explore how lipid rearrangements affect vesicle dynamics. Additionally, we highlight recent findings on lipid scramblases, particularly phospholipid scramblase-1 (PLSCR1), and their role in regulated exocytosis and compensatory endocytosis.

摘要

真核细胞的质膜高度动态且不对称组织。其持续重塑在多种细胞过程中起关键作用,包括细胞凋亡、血液凝固和囊泡运输。磷脂(PLs)在双层膜内的分布和重排受到严格调控,影响膜曲率、张力和组织。本综述研究了PL不对称性在囊泡融合(胞吐作用的最后一步)以及神经分泌细胞中通过补偿性内吞作用进行囊泡膜回收中的作用,特别强调了结构PLs,如磷脂酰胆碱(PC)、磷脂酰乙醇胺(PE)和磷脂酰丝氨酸(PS)。我们讨论了维持和破坏PLs不对称性的分子机制,并探讨了脂质重排如何影响囊泡动力学。此外,我们强调了关于脂质翻转酶,特别是磷脂翻转酶-1(PLSCR1)的最新发现,以及它们在调节性胞吐作用和补偿性内吞作用中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1310/12329543/bf7a94c95576/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1310/12329543/dce3ad846d33/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1310/12329543/bfd35905e244/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1310/12329543/bf7a94c95576/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1310/12329543/dce3ad846d33/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1310/12329543/bfd35905e244/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1310/12329543/bf7a94c95576/gr3.jpg

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本文引用的文献

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Angew Chem Int Ed Engl. 2025 Sep 1;64(36):e202510412. doi: 10.1002/anie.202510412. Epub 2025 Jul 25.
2
Cell membranes sustain phospholipid imbalance via cholesterol asymmetry.细胞膜通过胆固醇不对称性维持磷脂失衡。
Cell. 2025 May 15;188(10):2586-2602.e24. doi: 10.1016/j.cell.2025.02.034. Epub 2025 Apr 2.
3
Cholesterol affects the binding of proteins to phosphatidic acid without influencing its ionization properties.
胆固醇影响蛋白质与磷脂酸的结合,而不影响其电离特性。
J Lipid Res. 2025 Mar;66(3):100749. doi: 10.1016/j.jlr.2025.100749. Epub 2025 Jan 27.
4
Substrates, regulation, cellular functions, and disease associations of P4-ATPases.P4-ATP酶的底物、调控、细胞功能及疾病关联
Commun Biol. 2025 Jan 28;8(1):135. doi: 10.1038/s42003-025-07549-3.
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Synaptoneurolipidomics: lipidomics in the study of synaptic function.突触神经脂质组学:用于突触功能研究的脂质组学
Trends Biochem Sci. 2025 Feb;50(2):156-170. doi: 10.1016/j.tibs.2024.12.004. Epub 2025 Jan 2.
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