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外泌体摄取依赖于 ERK1/2-热休克蛋白 27 信号和脂质筏介导的内吞作用,而 caveolin-1 负调控该过程。

Exosome uptake depends on ERK1/2-heat shock protein 27 signaling and lipid Raft-mediated endocytosis negatively regulated by caveolin-1.

机构信息

Department of Clinical Sciences, Section of Oncology, Lund University, SE-22184 Lund, Sweden.

出版信息

J Biol Chem. 2013 Jun 14;288(24):17713-24. doi: 10.1074/jbc.M112.445403. Epub 2013 May 7.

Abstract

The role of exosomes in cancer can be inferred from the observation that they transfer tumor cell derived genetic material and signaling proteins, resulting in e.g. increased tumor angiogenesis and metastasis. However, the membrane transport mechanisms and the signaling events involved in the uptake of these virus-like particles remain ill-defined. We now report that internalization of exosomes derived from glioblastoma (GBM) cells involves nonclassical, lipid raft-dependent endocytosis. Importantly, we show that the lipid raft-associated protein caveolin-1 (CAV1), in analogy with its previously described role in virus uptake, negatively regulates the uptake of exosomes. We find that exosomes induce the phosphorylation of several downstream targets known to associate with lipid rafts as signaling and sorting platforms, such as extracellular signal-regulated kinase-1/2 (ERK1/2) and heat shock protein 27 (HSP27). Interestingly, exosome uptake appears dependent on unperturbed ERK1/2-HSP27 signaling, and ERK1/2 phosphorylation is under negative influence by CAV1 during internalization of exosomes. These findings significantly advance our general understanding of exosome-mediated uptake and offer potential strategies for how this pathway may be targeted through modulation of CAV1 expression and ERK1/2 signaling.

摘要

外泌体在癌症中的作用可以从以下观察中推断出来

它们传递肿瘤细胞衍生的遗传物质和信号蛋白,导致例如肿瘤血管生成和转移增加。然而,涉及这些类病毒颗粒摄取的膜转运机制和信号事件仍未得到明确定义。我们现在报告,从神经胶质瘤 (GBM) 细胞衍生的外泌体的内化涉及非经典的、依赖脂筏的内吞作用。重要的是,我们表明,脂筏相关蛋白 caveolin-1 (CAV1) 与先前描述的其在病毒摄取中的作用类似,负调节外泌体的摄取。我们发现外泌体诱导几种已知与脂筏作为信号和分拣平台相关的下游靶标的磷酸化,如细胞外信号调节激酶-1/2 (ERK1/2) 和热休克蛋白 27 (HSP27)。有趣的是,外泌体摄取似乎依赖于未受干扰的 ERK1/2-HSP27 信号,并且 CAV1 在摄取外泌体时对外泌体摄取的 ERK1/2 磷酸化产生负影响。这些发现显著提高了我们对外泌体介导摄取的一般理解,并为如何通过调节 CAV1 表达和 ERK1/2 信号来靶向该途径提供了潜在策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb7a/3682571/3ee34b9faef9/zbc0291353460001.jpg

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