Selective transfer of exosomes from oligodendrocytes to microglia by macropinocytosis

Dirk Fitzner(Max Planck Institute of Experimental Medicine), Mareike Schnaars(Max Planck Institute of Experimental Medicine), Denise van Rossum(University of Göttingen), Gurumoorthy Krishnamoorthy(Max Planck Institute of Neurobiology), Payam Dibaj(University of Göttingen), Mostafa Bakhti(Max Planck Institute of Experimental Medicine), Tommy Regen(University of Göttingen), Uwe‐Karsten Hanisch(University of Göttingen), Mikael Simons(Max Planck Institute of Experimental Medicine)
Journal of Cell Science
January 17, 2011
Cited by 793Open Access
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Abstract

The transfer of antigens from oligodendrocytes to immune cells has been implicated in the pathogenesis of autoimmune diseases. Here, we show that oligodendrocytes secrete small membrane vesicles called exosomes, which are specifically and efficiently taken up by microglia both in vitro and in vivo. Internalisation of exosomes occurs by a macropinocytotic mechanism without inducing a concomitant inflammatory response. After stimulation of microglia with interferon-γ, we observe an upregulation of MHC class II in a subpopulation of microglia. However, exosomes are preferentially internalised in microglia that do not seem to have antigen-presenting capacity. We propose that the constitutive macropinocytotic clearance of exosomes by a subset of microglia represents an important mechanism through which microglia participate in the degradation of oligodendroglial membrane in an immunologically 'silent' manner. By designating the capacity for macropinocytosis and antigen presentation to distinct cells, degradation and immune function might be assigned to different subtypes of microglia.


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