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跨高尔基体网络与内体系统之间的双向运输。

Bidirectional transport between the trans-Golgi network and the endosomal system.

作者信息

Anitei Mihaela, Wassmer Thomas, Stange Christoph, Hoflack Bernard

机构信息

Biotechnology Center, Dresden University of Technology, Tatzberg, Dresden, Germany.

出版信息

Mol Membr Biol. 2010 Nov;27(8):443-56. doi: 10.3109/09687688.2010.522601. Epub 2010 Nov 5.

Abstract

The exchange of proteins and lipids between the trans-Golgi network (TGN) and the endosomal system requires multiple cellular machines, whose activities are coordinated in space and time to generate pleomorphic, tubulo-vesicular carriers that deliver their content to their target compartments. These machines and their associated protein networks are recruited and/or activated on specific membrane domains where they select proteins and lipids into carriers, contribute to deform/elongate and partition membrane domains using the mechanical forces generated by actin polymerization or movement along microtubules. The coordinated action of these protein networks contributes to regulate the dynamic state of multiple receptors recycling between the cell surface, endosomes and the TGN, to maintain cell homeostasis as exemplified by the biogenesis of lysosomes and related organelles, and to establish/maintain cell polarity. The dynamic assembly and disassembly of these protein networks mediating the exchange of membrane domains between the TGN and endosomes regulates cell-cell signalling and thus the development of multi-cellular organisms. Somatic mutations in single network components lead to changes in transport dynamics that may contribute to pathological modifications underlying several human diseases such as mental retardation.

摘要

反式高尔基体网络(TGN)与内体系统之间蛋白质和脂质的交换需要多种细胞机制,这些机制的活动在空间和时间上相互协调,以生成多形性的管状囊泡载体,将其内容物输送到目标区室。这些机制及其相关的蛋白质网络在特定的膜结构域上被招募和/或激活,在那里它们将蛋白质和脂质选择到载体中,利用肌动蛋白聚合产生的机械力或沿微管的移动促使膜结构域变形/伸长并进行分隔。这些蛋白质网络的协同作用有助于调节多种受体在细胞表面、内体和TGN之间循环的动态状态,以维持细胞内稳态,如溶酶体及相关细胞器的生物发生所示例的那样,并建立/维持细胞极性。这些介导TGN和内体之间膜结构域交换的蛋白质网络的动态组装和解聚调节细胞间信号传导,从而影响多细胞生物的发育。单个网络组件中的体细胞突变会导致运输动力学的变化,这可能会促成一些人类疾病(如智力迟钝)潜在的病理改变。

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