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免疫细胞中的蛋白质运输。

Protein trafficking in immune cells.

机构信息

Department of Cell and Developmental Biology, Sackler School of Medicine, Tel Aviv University, Tel Aviv 69978, Israel.

出版信息

Immunobiology. 2009;214(7):507-25. doi: 10.1016/j.imbio.2008.11.011.

Abstract

The majority of cells of the immune system are specialized secretory cells, whose function depends on regulated exocytosis. The latter is mediated by vesicular transport involving the sorting of specialized cargo into the secretory granules (SGs), thereby generating the transport vesicles; their transport along the microtubules and eventually their signal-dependent fusion with the plasma membrane. Each of these steps is tightly controlled by mechanisms, which involve the participation of specific sorting signals on the cargo proteins and their recognition by cognate adaptor proteins, posttranslational modifications of the cargo proteins and multiple GTPases and SNARE proteins. In some of the cells (i.e. mast cells, T killer cells) an intimate connection exists between the secretory system and the endocytic one, whereby the SGs are lysosome related organelles (LROs) also referred to as secretory lysosomes. Herein, we discuss these mechanisms in health and disease states.

摘要

免疫系统的大多数细胞都是专门的分泌细胞,其功能取决于受调控的胞吐作用。后者由涉及将特殊货物分拣到分泌颗粒(SGs)中的囊泡运输介导,从而产生运输囊泡;它们沿着微管运输,最终在信号依赖性的情况下与质膜融合。这些步骤中的每一个都受到机制的严格控制,其中涉及货物蛋白上特定分拣信号的参与及其与同源衔接蛋白的识别、货物蛋白的翻译后修饰以及多种 GTPase 和 SNARE 蛋白。在一些细胞(即肥大细胞、T 杀伤细胞)中,分泌系统和内吞系统之间存在密切联系,其中 SGs 是溶酶体相关细胞器(LROs),也称为分泌溶酶体。本文中,我们将讨论这些在健康和疾病状态下的机制。

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