4.6 Review

Exosome-mediated amplification of endogenous brain repair mechanisms and brain and systemic organ interaction in modulating neurological outcome after stroke

期刊

JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM
卷 38, 期 12, 页码 2165-2178

出版社

SAGE PUBLICATIONS INC
DOI: 10.1177/0271678X18782789

关键词

Exosome; microRNA; neurorestoration; neurovascular niche; stroke

资金

  1. National Institute of Neurological Disorders and Stroke [R01NS083078, R01NS099030, R01NS097747, R01NS 088656]
  2. National Institutes of Health [R01HL143432]
  3. American Heart Association [17POST33 410580]
  4. NATIONAL HEART, LUNG, AND BLOOD INSTITUTE [R01HL143432] Funding Source: NIH RePORTER
  5. NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [R01NS083078, R01NS088656, R01NS097747, R01NS099030] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Ischemic stroke is caused by a regional interruption of cerebral blood flow to the brain. Rigorous pre-clinical and clinical research has made landmark progress in stroke treatment using thrombolytics and endovascular thrombectomy. Although numerous successful neuroprotective therapeutic agents for ischemic stroke have been reported in pre-clinical studies, most of them failed in clinical testing. Persistent pre-clinical research has demonstrated that the ischemic brain is not only passively dying but is also actively recovering. Within the neurovascular niche in the peri-infarct tissue, repair mechanisms thrive on the interactions between the neural and vascular compartments. In this review, we discuss exogenous therapy using mesenchymal stromal cell-derived exosomes to amplify endogenous brain repair mechanisms and to induce neurorestorative effects after stroke. Emerging evidence indicates that multiple communication axes between the various organs such as the brain, heart, kidney and gut, and whole body immune response mediated by the spleen can also affect stroke outcome. Therefore, in this review, we summarize this evidence and initiate a discussion on the potential to improve stroke outcome by amplifying multiple brain repair mechanisms after stroke, and by targeting peripheral organs and downstream events to enhance recovery in the injured brain and promote over all well being.

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