4.6 Review

Pericyte Structural Remodeling in Cerebrovascular Health and Homeostasis

期刊

FRONTIERS IN AGING NEUROSCIENCE
卷 10, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fnagi.2018.00210

关键词

pericyte; two-photon imaging; capillary blood flow; blood-brain barrier; Alzheimer's disease; mural cell; stroke; neurovascular coupling

资金

  1. National Institutes of Health (NIH)/NINDS [R01NS085402, R21NS096997, P20GM109040]
  2. National Science Foundation [1539034]
  3. American Heart Association [14GRNT20480366]
  4. Alzheimer's Association [2016-NIRG-397149]
  5. NIH/NINDS [F30NS096868]
  6. NIH/NIA [R21AG052321]
  7. NIH/NHLBI [R01HL123650, R01HL121877, R01HL133723]
  8. Loie Power Robinson Stem Cell and Regenerative Medicine Fund
  9. Seattle Children's Research Institute

向作者/读者索取更多资源

The biology of brain microvascular pericytes is an active area of research and discovery, as their interaction with the endothelium is critical for multiple aspects of cerebrovascular function. There is growing evidence that pericyte loss or dysfunction is involved in the pathogenesis of Alzheimer's disease, vascular dementia, ischemic stroke and brain injury. However, strategies to mitigate or compensate for this loss remain limited. In this review, we highlight a novel finding that pericytes in the adult brain are structurally dynamic in vivo, and actively compensate for loss of endothelial coverage by extending their far-reaching processes to maintain contact with regions of exposed endothelium. Structural remodeling of pericytes may present an opportunity to foster pericyte-endothelial communication in the adult brain and should be explored as a potential means to counteract pericyte loss in dementia and cerebrovascular disease. We discuss the pathophysiological consequences of pericyte loss on capillary function, and the biochemical pathways that may control pericyte remodeling. We also offer guidance for observing pericytes in vivo, such that pericyte structural remodeling can be more broadly studied in mouse models of cerebrovascular disease.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据