Brain perivascular macrophages: characterization and functional roles in health and disease

被引:151
作者
Faraco, Giuseppe [1 ]
Park, Laibaik [1 ]
Anrather, Josef [1 ]
Iadecola, Costantino [1 ]
机构
[1] Weill Cornell Med, Feil Family Brain & Mind Res Inst, 407 E61st St, New York, NY 10065 USA
来源
JOURNAL OF MOLECULAR MEDICINE-JMM | 2017年 / 95卷 / 11期
关键词
Brain perivascular macrophages; Immune-to-brain signaling; Alzheimer's disease; Cerebrovascular regulation; CNS infections; CENTRAL-NERVOUS-SYSTEM; SCAVENGER RECEPTOR; MANNOSE RECEPTOR; CD163(+) MACROPHAGES/MICROGLIA; MENINGEAL MACROPHAGES; CELL-TYPES; MICROGLIA; EXPRESSION; DISTINCT; BARRIER;
D O I
10.1007/s00109-017-1573-x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Perivascular macrophages (PVM) are a distinct population of resident brain macrophages characterized by a close association with the cerebral vasculature. PVM migrate from the yolk sac into the brain early in development and, like microglia, are likely to be a self-renewing cell population that, in the normal state, is not replenished by circulating monocytes. Increasing evidence implicates PVM in several disease processes, ranging from brain infections and immune activation to regulation of the hypothalamic-adrenal axis and neurovascular-neurocognitive dysfunction in the setting of hypertension, Alzheimer disease pathology, or obesity. These effects involve crosstalk between PVM and cerebral endothelial cells, interaction with circulating immune cells, and/or production of reactive oxygen species. Overall, the available evidence supports the idea that PVM are a key component of the brain-resident immune system with broad implications for the pathogenesis of major brain diseases. A better understanding of the biology and pathobiology of PVM may lead to new insights and therapeutic strategies for a wide variety of brain diseases.
引用
收藏
页码:1143 / 1152
页数:10
相关论文
共 75 条
[1]   VASOPRESSINERGIC CONTROL OF PITUITARY ADRENOCORTICOTROPIN SECRETION COMES OF AGE [J].
ANTONI, FA .
FRONTIERS IN NEUROENDOCRINOLOGY, 1993, 14 (02) :76-122
[2]   Turnover of rat brain perivascular cells [J].
Bechmann, I ;
Kwidzinski, E ;
Kovac, AD ;
Simbürger, E ;
Horvath, T ;
Gimsa, U ;
Dirnagl, U ;
Priller, J ;
Nitsch, R .
EXPERIMENTAL NEUROLOGY, 2001, 168 (02) :242-249
[3]   Immune surveillance of mouse brain perivascular spaces by blood-borne macrophages [J].
Bechmann, I ;
Priller, J ;
Kovac, A ;
Böntert, M ;
Wehner, T ;
Klett, FF ;
Bohsung, J ;
Stuschke, M ;
Dirnagl, U ;
Nitsch, R .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2001, 14 (10) :1651-1658
[4]   The cerebrovascular dysfunction induced by slow pressor doses of angiotensin II precedes the development of hypertension [J].
Capone, Carmen ;
Faraco, Giuseppe ;
Park, Laibaik ;
Cao, Xian ;
Davisson, Robin L. ;
Iadecola, Costantino .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2011, 300 (01) :H397-H407
[5]   Novel Characterization of Monocyte-Derived Cell Populations in the Meninges and Choroid Plexus and Their Rates of Replenishment in Bone Marrow Chimeric Mice [J].
Chinnery, Holly R. ;
Ruitenberg, Marc J. ;
McMenamin, Paul G. .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 2010, 69 (09) :896-909
[6]   The Cellular Phase of Alzheimer's Disease [J].
De Strooper, Bart ;
Karran, Eric .
CELL, 2016, 164 (04) :603-615
[7]   A cytokine network involving brain-borne IL-1β, IL-1ra, IL-18, IL-6, and TNFα operates during long-term potentiation and learning [J].
del Rey, Adriana ;
Balschun, Detlef ;
Wetzel, Wolfram ;
Randolf, Anke ;
Besedovsky, Hugo O. .
BRAIN BEHAVIOR AND IMMUNITY, 2013, 33 :15-23
[8]  
Elmquist JK, 1997, J COMP NEUROL, V381, P119, DOI 10.1002/(SICI)1096-9861(19970505)381:2<119::AID-CNE1>3.0.CO
[9]  
2-6
[10]   The movers and shapers in immune privilege of the CNS [J].
Engelhardt, Britta ;
Vajkoczy, Peter ;
Weller, Roy O. .
NATURE IMMUNOLOGY, 2017, 18 (02) :123-131