Regulation of exosome secretion by Rab35 and its GTPase-activating proteins TBC1D10A-C.
Regulation of exosome secretion by Rab35 and its GTPase-activating proteins TBC1D10A-C.
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DOI：
10.1083/jcb.200911018
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发表时间：
2010-04-19
期刊：
影响因子：
--
通讯作者：
Simons M
中科院分区：
文献类型：
--
作者：
Hsu C;Morohashi Y;Yoshimura S;Manrique-Hoyos N;Jung S;Lauterbach MA;Bakhti M;Grønborg M;Möbius W;Rhee J;Barr FA;Simons M
A screen in oligodendrocytes establishes a Rab family member and its GAPs as regulators of exosome secretion by controlling endocytic vesicle docking with the plasma membrane. Oligodendrocytes secrete vesicles into the extracellular space, where they might play a role in neuron–glia communication. These exosomes are small vesicles with a diameter of 50–100 nm that are formed within multivesicular bodies and are released after fusion with the plasma membrane. The intracellular pathways that generate exosomes are poorly defined. Because Rab family guanosine triphosphatases (GTPases) together with their regulators are important membrane trafficking organizers, we investigated which Rab GTPase-activating proteins interfere with exosome release. We find that TBC1D10A–C regulate exosome secretion in a catalytic activity–dependent manner. We show that Rab35 is the target of TBC1D10A–C and that the inhibition of Rab35 function leads to intracellular accumulation of endosomal vesicles and impairs exosome secretion. Rab35 localizes to the surface of oligodendroglia in a GTP-dependent manner, where it increases the density of vesicles, suggesting a function in docking or tethering. These findings provide a basis for understanding the biogenesis and function of exosomes in the central nervous system.
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