Siglec-h on activated microglia for recognition and engulfment of glioma cells

被引:61
作者
Kopatz, Jens [1 ]
Beutner, Clara [1 ]
Welle, Kristian [1 ]
Bodea, Liviu G. [1 ]
Reinhardt, Julia [1 ]
Claude, Janine [1 ]
Linnartz-Gerlach, Bettina [1 ]
Neumann, Harald [1 ]
机构
[1] Univ Bonn, Fac Med, Inst Reconstruct Neurobiol, Neural Regenerat Grp, D-53127 Bonn, Germany
关键词
Siglec; microglia; glioma; glycocalyx; EMBRYONIC STEM-CELLS; IMMUNE-SYSTEM; SIALIC-ACID; DEATH; MACROPHAGES; CLEARANCE; RECEPTOR; DISEASE; DAP12; PHAGOCYTOSIS;
D O I
10.1002/glia.22501
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Sialic-acid-binding immunoglobulin-like lectin-h (Siglec-h) is a recently identified mouse-specific CD33-related Siglec that signals via DAP12/TYROBP. Expression of Siglec-h has been observed on plasmacytoid dendritic cells and microglia, but the ligand and the function of Siglec-h remained elusive. Here, we demonstrate gene transcription and protein expression of Siglec-h by mouse microglia after interferon- treatment or polarization into a M1-subtype. Microglial Siglec-h acted as phagocytosis receptor since targeting of microsphere beads to Siglec-h triggered their uptake into the microglia. The extracellular domain of Siglec-h protein bound to mouse glioma lines, but not to astrocytes or other normal mouse cells. Microglial cells stimulated to express Siglec-h engulfed intact glioma cells without prior induction of apoptosis and slightly reduced glioma cell number in culture. Phagocytosis of glioma cells by activated microglia was dependent on Siglec-h and its adapter molecule DAP12. Thus, data show that M1-polarized microglial cells can engulf glioma cells via a DAP12-mediated Siglec-h dependent mechanism.
引用
收藏
页码:1122 / 1133
页数:12
相关论文
共 42 条
[1]   Generation of microglial cells from mouse embryonic stem cells [J].
Beutner, Clara ;
Roy, Kristin ;
Linnartz, Bettina ;
Napoli, Isabella ;
Neumann, Harald .
NATURE PROTOCOLS, 2010, 5 (09) :1481-1494
[2]   Siglec-H is an IPC-specific receptor that modulates type IIFN secretion through DAP12 [J].
Blasius, AL ;
Cella, M ;
Maldonado, J ;
Takai, T ;
Colonna, M .
BLOOD, 2006, 107 (06) :2474-2476
[3]   Eaten alive! Cell death by primary phagocytosis: 'phagoptosis' [J].
Brown, Guy C. ;
Neher, Jonas J. .
TRENDS IN BIOCHEMICAL SCIENCES, 2012, 37 (08) :325-332
[4]   The brain tumor microenvironment (vol 59, pg 1169, 2011) [J].
Charles, Nikki A. ;
Holland, Eric C. ;
Gilbertson, Richard ;
Glass, Rainer ;
Kettenmann, Helmut .
GLIA, 2012, 60 (03) :502-514
[5]   Trems in the immune system and beyond [J].
Colonna, M .
NATURE REVIEWS IMMUNOLOGY, 2003, 3 (06) :445-453
[6]   Siglecs and their roles in the immune system [J].
Crocker, Paul R. ;
Paulson, James C. ;
Varki, Ajit .
NATURE REVIEWS IMMUNOLOGY, 2007, 7 (04) :255-266
[7]  
Dall'olio F, 2012, AGEING RES REV
[8]   Buried alive: a novel approach to cancer treatment [J].
Fadeel, B ;
Orrenius, S ;
Pervaiz, S .
FASEB JOURNAL, 2004, 18 (01) :1-4
[9]   The Cell Biology of Phagocytosis [J].
Flannagan, Ronald S. ;
Jaumouille, Valentin ;
Grinstein, Sergio .
ANNUAL REVIEW OF PATHOLOGY: MECHANISMS OF DISEASE, VOL 7, 2012, 7 :61-98
[10]   Signal Regulatory Protein-β1 A Microglial Modulator of Phagocytosis in Alzheimer's Disease [J].
Gaikwad, Sadanand ;
Larionov, Sergey ;
Wang, Yiner ;
Dannenberg, Holger ;
Matozaki, Takashi ;
Monsonego, Alon ;
Thal, Dietmar R. ;
Neumann, Harald .
AMERICAN JOURNAL OF PATHOLOGY, 2009, 175 (06) :2528-2539