Mittelbrunn Maria, Vicente Manzanares Miguel, Sánchez-Madrid Francisco
Vascular Biology and Inflammation Department, Centro Nacional Investigaciones Cardiovasculares (CNIC), Madrid, 28029, Spain.
Universidad Autonoma de Madrid, Department of Medicine / IIS-Princesa, Diego de Leon 62, Madrid, Spain.
Traffic. 2015 Apr;16(4):327-337. doi: 10.1111/tra.12258. Epub 2015 Mar 3.
Exosomes are extracellular vesicles that transport different molecules between cells. They are formed and stored inside multivesicular bodies (MVB) until they are released to the extracellular environment. MVB fuse along the plasma membrane, driving non-polarized secretion of exosomes. However, polarized signaling potentially directs MVBs to a specific point in the plasma membrane to mediate a focal delivery of exosomes. MVB polarization occurs across a broad set of cellular situations, e.g. in immune and neuronal synapses, cell migration and in epithelial sheets. In this review, we summarize the current state of the art of polarized MVB docking and the specification of secretory sites at the plasma membrane. The current view is that MVB positioning and subsequent exosome delivery requires a polarizing, cytoskeletal dependent-trafficking mechanism. In this context, we propose scenarios in which biochemical and mechanical signals could drive the polarized delivery of exosomes in highly polarized cells, such as lymphocytes, neurons and epithelia.
外泌体是在细胞间运输不同分子的细胞外囊泡。它们在多泡体(MVB)内形成并储存,直至释放到细胞外环境中。MVB沿质膜融合,驱动外泌体的非极化分泌。然而,极化信号可能将MVB引导至质膜上的特定点,以介导外泌体的局部递送。MVB极化发生在广泛的细胞情况下,例如在免疫和神经元突触、细胞迁移以及上皮层中。在本综述中,我们总结了极化MVB对接以及质膜上分泌位点特异性的当前研究现状。目前的观点是,MVB定位及随后的外泌体递送需要一种极化的、细胞骨架依赖性的运输机制。在此背景下,我们提出了一些情形,其中生化和机械信号可能驱动外泌体在高度极化的细胞(如淋巴细胞、神经元和上皮细胞)中的极化递送。