دورية أكاديمية

Exendin-4 promotes actin cytoskeleton rearrangement and protects cells from Nogo-A-Δ20 mediated spreading inhibition and growth cone collapse by down-regulating RhoA expression and activation via the PI3K pathway

التفاصيل البيبلوغرافية
العنوان: Exendin-4 promotes actin cytoskeleton rearrangement and protects cells from Nogo-A-Δ20 mediated spreading inhibition and growth cone collapse by down-regulating RhoA expression and activation via the PI3K pathway
المؤلفون: Fei Zhao, jianwei Li, Renjie Wang, Huiyou Xu, Ke Ma, Xianbin Kong, Zhonglei Sun, Xuegang Niu, Jipeng Jiang, Baohu Liu, Bo Li, Feng Duan, Xuyi Chen
المصدر: Biomedicine & Pharmacotherapy, Vol 109, Iss , Pp 135-143 (2019)
بيانات النشر: Elsevier, 2019.
سنة النشر: 2019
المجموعة: LCC:Therapeutics. Pharmacology
مصطلحات موضوعية: Exendin-4, Nogo-A-Δ20, RhoA, Cell spreading, Growth cone, Cell migration, Therapeutics. Pharmacology, RM1-950
الوصف: Exendin-4 is a protein of the GLP-1 family currently used to treat diabetes. Recently, a greater number of biological properties have been associated with the GLP-1 family. Our data shows that exendin-4 treatment significantly increases the cytoskeleton rearrangement, which leads to an increasingly differentiated phenotype and reduced cell migration. We also found that exendin-4 could prevent SH-SY5Y and PC12 cells from Nogo-A-Δ20 mediated spreading inhibition and neurite collapse. Western blot analysis indicated that exendin-4 treatment both reduced the expression and activation of RhoA via the PI3K signaling pathway. These data suggest that exendin-4 may protect nerve regeneration by preventing the inhibition of Nogo-A via down-regulating RhoA expression and activation.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 0753-3322
Relation: http://www.sciencedirect.com/science/article/pii/S0753332218346195; https://doaj.org/toc/0753-3322
DOI: 10.1016/j.biopha.2018.10.008
URL الوصول: https://doaj.org/article/d7f5f70ce35f4c29acb266061e4fbd4e
رقم الأكسشن: edsdoj.7f5f70ce35f4c29acb266061e4fbd4e
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:07533322
DOI:10.1016/j.biopha.2018.10.008