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神经递质触发的外泌体转移介导少突胶质细胞-神经元通讯。

Neurotransmitter-triggered transfer of exosomes mediates oligodendrocyte-neuron communication.

机构信息

Department of Molecular Cell Biology, University of Mainz, Mainz, Germany.

出版信息

PLoS Biol. 2013 Jul;11(7):e1001604. doi: 10.1371/journal.pbio.1001604. Epub 2013 Jul 9.

Abstract

Reciprocal interactions between neurons and oligodendrocytes are not only crucial for myelination, but also for long-term survival of axons. Degeneration of axons occurs in several human myelin diseases, however the molecular mechanisms of axon-glia communication maintaining axon integrity are poorly understood. Here, we describe the signal-mediated transfer of exosomes from oligodendrocytes to neurons. These endosome-derived vesicles are secreted by oligodendrocytes and carry specific protein and RNA cargo. We show that activity-dependent release of the neurotransmitter glutamate triggers oligodendroglial exosome secretion mediated by Ca²⁺ entry through oligodendroglial NMDA and AMPA receptors. In turn, neurons internalize the released exosomes by endocytosis. Injection of oligodendroglia-derived exosomes into the mouse brain results in functional retrieval of exosome cargo in neurons. Supply of cultured neurons with oligodendroglial exosomes improves neuronal viability under conditions of cell stress. These findings indicate that oligodendroglial exosomes participate in a novel mode of bidirectional neuron-glia communication contributing to neuronal integrity.

摘要

神经元和少突胶质细胞之间的相互作用不仅对髓鞘形成至关重要,而且对轴突的长期存活也至关重要。在几种人类髓鞘疾病中都会发生轴突变性,但是维持轴突完整性的轴突-胶质细胞通讯的分子机制尚不清楚。在这里,我们描述了少突胶质细胞到神经元的信号介导的外体转移。这些内体衍生的囊泡由少突胶质细胞分泌,并携带特定的蛋白质和 RNA 货物。我们表明,神经递质谷氨酸的活性依赖性释放会触发通过少突胶质细胞 NMDA 和 AMPA 受体的钙离子内流介导的少突胶质细胞外体分泌。反过来,神经元通过内吞作用内化释放的外体。将少突胶质细胞衍生的外体注射到小鼠脑中会导致神经元中内体货物的功能恢复。在细胞应激条件下,用少突胶质细胞外体供给培养的神经元可提高神经元活力。这些发现表明,少突胶质细胞外体参与了一种新的双向神经元-胶质细胞通讯模式,有助于神经元的完整性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7197/3706306/4076f04aeae8/pbio.1001604.g001.jpg

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