| Literature DB >> 29673933 |
Chao Wang1, Jie Zhang1, Junchun Tang2, Yi-Yi Li1, YanXia Gu1, Ying Yu1, Jing Xiong1, Xueqing Zhao1, Zheng Zhang1, Ting-Ting Li1, Jutao Chen1, Qi Wan3, Zhaohui Zhang4.
Abstract
Lysophosphatidic acid (LPA), an extracellular signaling molecule, influences diverse biological events, including the pathophysiological process induced after ischemic brain injury. However, the molecular mechanisms mediating the pathological change after ischemic stroke remain elusive. Here we report that asparagine endopeptidase (AEP), a lysosomal cysteine proteinase, is regulated by LPA during stroke. AEP proteolytically cleaves tau and generates tauN368 fragments, triggering neuronal death. Inhibiting the generation of LPA reduces the expression of AEP and tauN368, and alleviates neuronal cell death. Together, this evidence indicates that the LPA-AEP pathway plays a key role in the pathophysiological process induced after ischemic stroke. Inhibition of LPA could be a useful therapeutic for treating neuronal injury after stroke.Entities:
Keywords: AEP; Ischemic stroke; LPA; Tau
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Year: 2018 PMID: 29673933 DOI: 10.1016/j.expneurol.2018.04.010
Source DB: PubMed Journal: Exp Neurol ISSN: 0014-4886 Impact factor: 5.330