4.4 Article

Functional implications of the association of tau with the plasma membrane

期刊

BIOCHEMICAL SOCIETY TRANSACTIONS
卷 38, 期 -, 页码 1012-1015

出版社

PORTLAND PRESS LTD
DOI: 10.1042/BST0381012

关键词

Alzheimer's disease; kinase; membrane; phosphorylation; tau; trafficking

资金

  1. Medical Research Council
  2. Henry Smith Charity
  3. Medical Research Council [G0300408] Funding Source: researchfish
  4. MRC [G0300408] Funding Source: UKRI

向作者/读者索取更多资源

Tau is an abundant microtubule-associated protein which regulates the stability of the cytoskeleton. Tau binds microtubules directly through microtubule-binding domains in its C-terminus. However, tau is not only located in the cytosol of cells, but also associated with other intracellular domains, including the plasma membrane, suggesting that tau may have additional functions other than stabilizing the neuronal cytoskeleton. Localization of tau at the cell surface appears to be dependent on interactions of the N-terminal projection domain of tau. Furthermore, membrane-associated tau is dephosphorylated at serine/threonine residues, suggesting that the phosphorylation state of tau regulates its intracellular trafficking. Dephosphorylation of tau may increase the association of tau with trafficking proteins which target tau to the plasma membrane. Thus it is possible that the hyperphosphoryation of tau may contribute to the pathogenesis of Alzheimer's disease by promoting the formation of neurofibrillary tangles from cytosolic tau, and also by inhibiting additional tau functions through disruption of its targeting to the plasma membrane.

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

4.4
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