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径向体外冲击波治疗通过 Notch、PI3K/AKT 和 Wnt/β-catenin 信号增强神经干细胞的增殖和分化。

Radial Extracorporeal Shock Wave Therapy Enhances the Proliferation and Differentiation of Neural Stem Cells by Notch, PI3K/AKT, and Wnt/β-catenin Signaling.

机构信息

Department of Rehabilitation Medicine, The First Hospital of China Medical University, Shenyang, Liaoning, PR China.

Institute of Meta-Synthesis Medicine, Beijing, China.

出版信息

Sci Rep. 2017 Nov 10;7(1):15321. doi: 10.1038/s41598-017-15662-5.

DOI:10.1038/s41598-017-15662-5
PMID:29127399
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5681501/
Abstract

Neural stem cell (NSC) proliferation and differentiation play a pivotal role in the repair of brain function in central nervous system (CNS) diseases. Radial extracorporeal shock wave therapy (rESWT) is a non-invasive and innovative treatment for many conditions, yet little is known about the effects of this treatment on NSCs. Mouse NSCs (NE-4C) were exposed to rESWT with 1.0, 1.5, 2.0, 2.5, 3.0, and 3.5 bar (500 impulses, and 2 Hz) in vitro. Cell viability test results indicated that rESWT, at a dose of 2.5 bar, 500 impulses, and 2 Hz, increased NE-4C viability within 72 h, and that the PI3K/AKT pathway was involved in its mechanisms. Exposure to rESWT also affected proliferation and differentiation of NE-4C after 8 weeks, which may be associated with Wnt/β-catenin and Notch pathways. This assessment is corroborated by the ability of inhibitors of Wnt/β-catenin [Dickkopf-1 (Dkk-1)] and the Notch pathway (DAPT) to weaken proliferation and differentiation of NSCs. In summary, a proper dose of rESWT enhanced NSCs augment via the PI3K/AKT pathway initially. Also, Wnt/β-catenin and the Notch pathway play important roles in regulation of the long-term efficacy of rESWT. This study reveals a novel approach to culture NSCs in vitro and support neurogenesis.

摘要

神经干细胞 (NSC) 的增殖和分化在中枢神经系统 (CNS) 疾病的脑功能修复中起着关键作用。体外冲击波治疗 (rESWT) 是一种非侵入性和创新的治疗方法,可用于多种疾病,但对于这种治疗方法对 NSCs 的影响知之甚少。将小鼠 NSCs (NE-4C) 暴露于 rESWT 中,采用 1.0、1.5、2.0、2.5、3.0 和 3.5 巴(500 个脉冲,2 Hz)进行体外治疗。细胞活力测试结果表明,在 2.5 巴、500 个脉冲和 2 Hz 的剂量下,rESWT 在 72 小时内增加了 NE-4C 的活力,并且该过程涉及 PI3K/AKT 通路。暴露于 rESWT 还会影响 NE-4C 8 周后的增殖和分化,这可能与 Wnt/β-catenin 和 Notch 通路有关。Wnt/β-catenin 通路的抑制剂 [Dickkopf-1 (Dkk-1)] 和 Notch 通路的抑制剂 (DAPT) 削弱 NSCs 的增殖和分化,这进一步证实了上述结果。总之,适当剂量的 rESWT 通过 PI3K/AKT 通路最初增强 NSCs 的活力。此外,Wnt/β-catenin 和 Notch 通路在调节 rESWT 的长期疗效中发挥着重要作用。本研究揭示了一种新的体外培养 NSCs 并支持神经发生的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/783a/5681501/74d5440d675b/41598_2017_15662_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/783a/5681501/95cff3117f0a/41598_2017_15662_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/783a/5681501/070f0598527e/41598_2017_15662_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/783a/5681501/f47eec2da68b/41598_2017_15662_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/783a/5681501/d40c89a94b8e/41598_2017_15662_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/783a/5681501/75472f6ab275/41598_2017_15662_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/783a/5681501/8c1bd639ac69/41598_2017_15662_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/783a/5681501/67e34a3775e1/41598_2017_15662_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/783a/5681501/74d5440d675b/41598_2017_15662_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/783a/5681501/95cff3117f0a/41598_2017_15662_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/783a/5681501/070f0598527e/41598_2017_15662_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/783a/5681501/f47eec2da68b/41598_2017_15662_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/783a/5681501/d40c89a94b8e/41598_2017_15662_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/783a/5681501/75472f6ab275/41598_2017_15662_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/783a/5681501/8c1bd639ac69/41598_2017_15662_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/783a/5681501/67e34a3775e1/41598_2017_15662_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/783a/5681501/74d5440d675b/41598_2017_15662_Fig8_HTML.jpg

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