Macrophage phagocytosis after spinal cord injury: when friends become foes

被引:102
作者
Van Broeckhoven, Jana [1 ]
Sommer, Daniela [1 ]
Dooley, Dearbhaile [2 ,3 ]
Hendrix, Sven [1 ,4 ]
Franssen, Aimee J. P. M. [1 ]
机构
[1] Hasselt Univ, Biomed Res Inst, Dept Immunol & Infect, Diepenbeek, Belgium
[2] Univ Coll Dublin, Hlth Sci Ctr, Sch Med, Dublin 4, Ireland
[3] Univ Coll Dublin, UCD Conway Inst Biomol & Biomed Res, Dublin 4, Ireland
[4] Med Sch Hamburg, Hamburg, Germany
关键词
CNS trauma; phagocytosis; foam cells; axonal dieback; technical challenges; MANNOSE RECEPTOR EXPRESSION; GREEN FLUORESCENT PROTEIN; APOPTOTIC CELLS; MYELIN PHAGOCYTOSIS; AXONAL DIEBACK; C1Q-MEDIATED ENHANCEMENT; ALTERNATIVE ACTIVATION; WALLERIAN DEGENERATION; SCAVENGER-RECEPTOR; DEBRIS CLEARANCE;
D O I
10.1093/brain/awab250
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
After spinal cord injury, macrophages can exert either beneficial or detrimental effects depending on their phenotype. Aside from their critical role in inflammatory responses, macrophages are also specialized in the recognition, engulfment, and degradation of pathogens, apoptotic cells, and tissue debris. They promote remyelination and axonal regeneration by removing inhibitory myelin components and cellular debris. However, excessive intracellular presence of lipids and dysregulated intracellular lipid homeostasis result in the formation of foamy macrophages. These develop a pro-inflammatory phenotype that may contribute to further neurological decline. Additionally, myelin-activated macrophages play a crucial role in axonal dieback and retraction. Here, we review the opposing functional consequences of phagocytosis by macrophages in spinal cord injury, including remyelination and regeneration versus demyelination, degeneration, and axonal dieback. Furthermore, we discuss how targeting the phagocytic ability of macrophages may have therapeutic potential for the treatment of spinal cord injury.
引用
收藏
页码:2933 / 2945
页数:13
相关论文
共 152 条
[1]   Traumatic Spinal Cord Injury: An Overview of Pathophysiology, Models and Acute Injury Mechanisms [J].
Alizadeh, Arsalan ;
Dyck, Scott Matthew ;
Karimi-Abdolrezaee, Soheila .
FRONTIERS IN NEUROLOGY, 2019, 10
[2]   Phagocytosis of apoptotic cells in homeostasis [J].
Arandjelovic, Sanja ;
Ravichandran, Kodi S. .
NATURE IMMUNOLOGY, 2015, 16 (09) :907-917
[3]   Regulation of Apoptotic Cell Clearance During Resolution of Inflammation [J].
Arienti, Simone ;
Barth, Nicole D. ;
Dorward, David A. ;
Rossi, Adriano G. ;
Dransfield, Ian .
FRONTIERS IN PHARMACOLOGY, 2019, 10
[4]   Myelin-mediated inhibition of oligodendrocyte precursor differentiation can be overcome by pharmacological modulation of Fyn-RhoA and protein kinase C signalling [J].
Baer, Alexandra S. ;
Syed, Yasir A. ;
Kang, Sung Ung ;
Mitteregger, Dieter ;
Vig, Raluca ;
Ffrench-Constant, Charles ;
Franklin, Robin J. M. ;
Altmann, Friedrich ;
Lubec, Gert ;
Kotter, Mark R. .
BRAIN, 2009, 132 :465-481
[5]   The Interaction Between Signal Regulatory Protein Alpha (SIRPα) and CD47: Structure, Function, and Therapeutic Target [J].
Barclay, A. Neil ;
van den Berg, Timo K. .
ANNUAL REVIEW OF IMMUNOLOGY, VOL 32, 2014, 32 :25-50
[6]  
Beattie MS, 2002, PROG BRAIN RES, V137, P37
[7]  
BECERRA JL, 1995, AM J NEURORADIOL, V16, P125
[8]   New tools for studying microglia in the mouse and human CNS [J].
Bennett, Mariko L. ;
Bennett, F. Chris ;
Liddelow, Shane A. ;
Ajami, Bahareh ;
Zamanian, Jennifer L. ;
Fernhoff, Nathaniel B. ;
Mulinyawe, Sara B. ;
Bohlen, Christopher J. ;
Adil, Aykezar ;
Tucker, Andrew ;
Weissman, Irving L. ;
Chang, Edward F. ;
Li, Gordon ;
Grant, Gerald A. ;
Gephart, Melanie G. Hayden ;
Barres, Ben A. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2016, 113 (12) :E1738-E1746
[9]   Integration of metabolism and inflammation by lipid-activated nuclear receptors [J].
Bensinger, Steven J. ;
Tontonoz, Peter .
NATURE, 2008, 454 (7203) :470-477
[10]   Ephrin-B3 is a myelin-based inhibitor of neurite outgrowth [J].
Benson, MD ;
Romero, MI ;
Lush, ME ;
Lu, QR ;
Henkemeyer, M ;
Parada, LF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (30) :10694-10699