Selective transfer of exosomes from oligodendrocytes to microglia by macropinocytosis

被引:659
作者
Fitzner, Dirk [1 ]
Schnaars, Mareike [1 ,2 ]
van Rossum, Denise [3 ]
Krishnamoorthy, Gurumoorthy [4 ]
Dibaj, Payam [2 ]
Bakhti, Mostafa [1 ]
Regen, Tommy [3 ]
Hanisch, Uwe-Karsten [3 ]
Simons, Mikael [1 ,2 ]
机构
[1] Max Planck Inst Expt Med, D-37075 Gottingen, Germany
[2] Univ Gottingen, Dept Neurol, D-37075 Gottingen, Germany
[3] Univ Gottingen, Inst Neuropathol, D-37075 Gottingen, Germany
[4] Max Planck Inst Neurobiol, Dept Neuroimmunol, D-82152 Martinsried, Germany
关键词
Macropinocytosis; Microglia; Myelin; Oligodendrocytes; Exosomes; MEDIATED MYELIN PHAGOCYTOSIS; MULTIPLE-SCLEROSIS; DENDRITIC CELLS; MEMBRANE-VESICLES; DOWN-REGULATION; IN-VITRO; T-CELLS; RECEPTOR; BETA; MACROPHAGES;
D O I
10.1242/jcs.074088
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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-gamma, 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.
引用
收藏
页码:447 / 458
页数:12
相关论文
共 68 条
[1]   Myelin oligodendrocyte glycoprotein-specific T cell receptor transgenic mice develop spontaneous autoimmune optic neuritis [J].
Bettelli, E ;
Pagany, M ;
Weiner, HL ;
Linington, C ;
Sobel, RA ;
Kuchroo, AK .
JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 197 (09) :1073-1081
[2]  
Beyer M, 2000, GLIA, V31, P262, DOI 10.1002/1098-1136(200009)31:3<262::AID-GLIA70>3.0.CO
[3]  
2-2
[4]   Exosomes released from infected macrophages contain mycobacterium avium glycopeptidolipids and are proinflammatory [J].
Bhatnagar, Sanchita ;
Schorey, Jeffrey S. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (35) :25779-25789
[5]   Acid sphingomyelinase activity triggers microparticle release from glial cells [J].
Bianco, Fabio ;
Perrotta, Cristiana ;
Novellino, Luisa ;
Francolini, Maura ;
Riganti, Loredana ;
Menna, Elisabetta ;
Saglietti, Laura ;
Schuchman, Edward H. ;
Furlan, Roberto ;
Clementi, Emilio ;
Matteoli, Michela ;
Verderio, Claudia .
EMBO JOURNAL, 2009, 28 (08) :1043-1054
[6]   Exosomes and HIV Gag bud from endosome-like domains of the T cell plasma membrane [J].
Booth, AM ;
Fang, Y ;
Fallon, JK ;
Yang, JM ;
Hildreth, JEK ;
Gould, SJ .
JOURNAL OF CELL BIOLOGY, 2006, 172 (06) :923-935
[7]   Inflammatory stimuli induce accumulation of MHC class II complexes on dendritic cells [J].
Cella, M ;
Engering, A ;
Pinet, V ;
Pieters, J ;
Lanzavecchia, A .
NATURE, 1997, 388 (6644) :782-787
[8]   Shedding microvesicles: artefacts no more [J].
Cocucci, Emanuele ;
Racchetti, Gabriella ;
Meldolesi, Jacopo .
TRENDS IN CELL BIOLOGY, 2009, 19 (02) :43-51
[9]   Non-PKC DAG/phorbol-ester receptor(s) inhibit complement receptor-3 and nPKC inhibit scavenger receptor-AI/II mediated myelin phagocytosis but cPKC, PI3K, and PLCγ activate myelin phagocytosis by both [J].
Cohen, G ;
Makranz, C ;
Spira, M ;
Kodama, T ;
Reichert, F ;
Rotshenker, S .
GLIA, 2006, 53 (05) :538-550
[10]   Schwann Cell to Axon Transfer of Ribosomes: Toward a Novel Understanding of the Role of Glia in the Nervous System [J].
Court, Felipe A. ;
Hendriks, William T. J. ;
MacGillavry, Harold D. ;
Alvarez, Jaime ;
Van Minnen, Jan .
JOURNAL OF NEUROSCIENCE, 2008, 28 (43) :11024-11029