Immune-Neurovascular Interactions in Experimental Perinatal and Childhood Arterial Ischemic Stroke

被引:0
|
作者
Mallard, Carina [2 ]
Ferriero, Donna M. [3 ,4 ]
Vexler, Zinaida S. [1 ,4 ]
机构
[1] Univ Calif San Francisco, Dept Neurol, 675 Nelson Rising Ln, San Francisco, CA 94158 USA
[2] Univ Gothenburg, Inst Neurosci & Physiol, Dept Physiol, Gothenburg, Sweden
[3] UCSF, Dept Pediat, San Francisco, CA USA
[4] UCSF, Weill Inst Neurosci, Dept Neurol, San Francisco, CA USA
关键词
blood-brain barrier; brain ischemia; infant; inflammation; leukocytes; microglia; BRAIN-BARRIER PERMEABILITY; N-3 PUFAS DEFICIENCY; REGULATORY T-CELLS; NEONATAL STROKE; DEPENDENT ACTIVATION; NEUTROPHIL ELASTASE; CEREBRAL-ISCHEMIA; CHOROID-PLEXUS; INJURY; RAT;
D O I
10.1161/STROKEAHA.123.043399
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Emerging clinical and preclinical data have demonstrated that the pathophysiology of arterial ischemic stroke in the adult, neonates, and children share similar mechanisms that regulate brain damage but also have distinct molecular signatures and involved cellular pathways due to the maturational stage of the central nervous system and the immune system at the time of the insult. In this review, we discuss similarities and differences identified thus far in rodent models of 2 different diseases-neonatal (perinatal) and childhood arterial ischemic stroke. In particular, we review acquired knowledge of the role of resident and peripheral immune populations in modulating outcomes in models of perinatal and childhood arterial ischemic stroke and the most recent and relevant findings in relation to the immune-neurovascular crosstalk, and how the influence of inflammatory mediators is dependent on specific brain maturation stages. Finally, we discuss the current state of treatments geared toward age-appropriate therapies that signal via the immune-neurovascular interaction and consider sex differences to achieve successful translation.
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页码:506 / 518
页数:13
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