Pericytes Control Key Neurovascular Functions and Neuronal Phenotype in the Adult Brain and during Brain Aging

被引:1203
作者
Bell, Robert D. [1 ,2 ]
Winkler, Ethan A. [1 ,2 ]
Sagare, Abhay P. [1 ,2 ]
Singh, Itender [1 ,2 ]
LaRue, Barb [1 ,2 ]
Deane, Rashid [1 ,2 ]
Zlokovic, Berislav V. [1 ,2 ]
机构
[1] Univ Rochester, Med Ctr, Dept Neurosurg, Ctr Neurodegenerat & Vasc Brain Disorders, Rochester, NY 14642 USA
[2] Univ Rochester, Med Ctr, Dept Neurol, Ctr Neurodegenerat & Vasc Brain Disorders, Rochester, NY 14642 USA
基金
美国国家卫生研究院;
关键词
AMYLOID-BETA PEPTIDE; PDGF-B; PROGENITOR CELLS; MOTOR-NEURONS; MOUSE MODELS; MUTANT MICE; BARRIER; DEFICIENT; RECEPTOR; EXPRESSION;
D O I
10.1016/j.neuron.2010.09.043
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Pericytes play a key role in the development of cerebral microcirculation. The exact role of pericytes in the neurovascular unit in the adult brain and during brain aging remains, however, elusive. Using adult viable pericyte-deficient mice, we show that pericyte loss leads to brain vascular damage by two parallel pathways: (1) reduction in brain microcirculation causing diminished brain capillary perfusion, cerebral blood flow, and cerebral blood flow responses to brain activation that ultimately mediates chronic perfusion stress and hypoxia, and (2) blood-brain barrier breakdown associated with brain accumulation of serum proteins and several vasculotoxic and/or neurotoxic macromolecules ultimately leading to secondary neuronal degenerative changes. We show that age-dependent vascular damage in pericyte-deficient mice precedes neuronal degenerative changes, learning and memory impairment, and the neuroinflammatory response. Thus, pericytes control key neurovascular functions that are necessary for proper neuronal structure and function, and pericyte loss results in a progressive age-dependent vascular-mediated neurodegeneration.
引用
收藏
页码:409 / 427
页数:19
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