| Literature DB >> 21242314 |
Dirk Fitzner1, Mareike Schnaars, Denise van Rossum, Gurumoorthy Krishnamoorthy, Payam Dibaj, Mostafa Bakhti, Tommy Regen, Uwe-Karsten Hanisch, Mikael Simons.
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.Entities:
Mesh:
Year: 2011 PMID: 21242314 DOI: 10.1242/jcs.074088
Source DB: PubMed Journal: J Cell Sci ISSN: 0021-9533 Impact factor: 5.285