4.7 Review

The Role of ADF/Cofilin in Synaptic Physiology and Alzheimer's Disease

期刊

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fcell.2020.594998

关键词

ADF; cofilin; dendritic spine; LTP; LTD; AMPA glutamate receptor

资金

  1. Canadian Institutes of Health Research [CIHR PJT155959, CIHR PJT168922]
  2. Canadian Natural Science and Engineering Research Council (NSERC) [RGPIN341498, RGPIN06295]
  3. Hospital for Sick Children Foundation
  4. Libyan-North American Scholarship
  5. University of Toronto Graduate Scholarship
  6. Dystonia Medical Research Foundation Canada

向作者/读者索取更多资源

Actin-depolymerization factor (ADF)/cofilin, a family of actin-binding proteins, are critical for the regulation of actin reorganization in response to various signals. Accumulating evidence indicates that ADF/cofilin also play important roles in neuronal structure and function, including long-term potentiation and depression. These are the most extensively studied forms of long-lasting synaptic plasticity and are widely regarded as cellular mechanisms underlying learning and memory. ADF/cofilin regulate synaptic function through their effects on dendritic spines and the trafficking of glutamate receptors, the principal mediator of excitatory synaptic transmission in vertebrates. Regulation of ADF/cofilin involves various signaling pathways converging on LIM domain kinases and slingshot phosphatases, which phosphorylate/inactivate and dephosphorylate/activate ADF/cofilin, respectively. Actin-depolymerization factor/cofilin activity is also regulated by other actin-binding proteins, activity-dependent subcellular distribution and protein translation. Abnormalities in ADF/cofilin have been associated with several neurodegenerative disorders such as Alzheimer's disease. Therefore, investigating the roles of ADF/cofilin in the brain is not only important for understanding the fundamental processes governing neuronal structure and function, but also may provide potential therapeutic strategies to treat brain disorders.

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

4.7
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