English  |  正體中文  |  简体中文  |  全文筆數/總筆數 : 47121/50987 (92%)
造訪人次 : 13821225      線上人數 : 255
RC Version 6.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
搜尋範圍 查詢小技巧:
  • 您可在西文檢索詞彙前後加上"雙引號",以獲取較精準的檢索結果
  • 若欲以作者姓名搜尋,建議至進階搜尋限定作者欄位,可獲得較完整資料
  • 進階搜尋
    主頁登入上傳說明關於CCUR管理 到手機版


    請使用永久網址來引用或連結此文件: https://irlib.pccu.edu.tw/handle/987654321/39381


    題名: Endoplasmic Reticulum Stress-Triggered Autophagy and Lysosomal Dysfunction Contribute to the Cytotoxicity of Amine-Modified Silver Nanoparticles in NIH 3T3 Cells
    作者: Lee, YH (Lee, Yu-Hsuan)
    Fang, CY (Fang, Chun-Yong)
    Chiu, HW (Chiu, Hui-Wen)
    Cheng, FY (Cheng, Fong-Yu)
    Tsai, JC (Tsai, Jui-Chen)
    Chen, CW (Chen, Chun-Wan)
    Wang, YJ (Wang, Ying-Jan)
    貢獻者: 化學系
    關鍵詞: Silver Nanoparticles
    Physico-Chemical Properties
    Cellular Uptake
    Endoplasmic Reticulum Stress
    Autophagy
    Lysosome Impairment
    日期: 2017-07
    上傳時間: 2018-02-21 15:49:17 (UTC+8)
    摘要: The mechanisms underlying nanoparticle-induced toxicity have become one of the most studied topics in toxicology during the last few years. Because of their excellent antimicrobial activity, silver nanoparticles (AgNPs) are recognized as promising nanomaterials with broad applicability. However, knowledge of the impact of AgNPs on biological systems, particularly regarding their possible effects and fate in living cells remains limited. Amines are among most popular AgNPs modifying agents. In this study, we found that amine-modified AgNPs could be taken up by cells through endocytosis. The internalized AgNPs eventually accumulated in lysosomes or autophagosomes. Smaller AgNPs (SAS, similar to 20 nm) were more toxic than larger AgNPs (LAS, similar to 80 nm). Our results suggest that SAS caused more lysosomal swelling, arrested autophagy and cell death. The mechanisms underlying the AgNP-induced autophagy in NIH 3T3 cells could be mediated by the activation of oxidative stress and endoplasmic reticulum (ER) stress signaling pathways. AgNPs treatment could trigger the expression of ER stress and autophagy markers (IRE1 and LC3-II). However, the autophagy substrate, p62, was accumulated in AgNP-treated cells, indicating that the autophagy process was inhibited. Our results clarify the mechanism by which AgNPs induce autophagosome accumulation and reveal the effects of AgNPs on lysosomes. This study illustrates the influence of AgNPs on biological systems and may provide insights to guide the development of protective measures for biomedical applications of AgNPs.
    關聯: JOURNAL OF BIOMEDICAL NANOTECHNOLOGY 卷: 13 期: 7 頁碼: 778-794
    顯示於類別:[化學系所] 期刊論文

    文件中的檔案:

    檔案 描述 大小格式瀏覽次數
    index.html0KbHTML196檢視/開啟


    在CCUR中所有的資料項目都受到原著作權保護.


    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - 回饋