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奈米金微粒對細胞毒性檢測技術及生物標記之篩選建立

中文摘要 全球奈米科技正如火如荼的發展,雖然此尖端科技在各個領域上開拓新的希望、應用價值與新興產品,然而這些具有奈米結構的物質,其本身的化學性質與物理性質,會隨著粒徑大小的不同而有所變化,對人體的毒性危害或影響也可能有所改變,因此對於安全衛生環保亦將可能產生重大的衝擊。本研究團隊在過去的計劃中建立以細胞連續及即時生長分析儀為奈米物質的細胞毒性之篩選平台,此項新的檢測方法,可以免除傳統細胞毒性測試方法之染劑或指示劑的使用,進而降低其與奈米物干擾所產生之不一致結果,並可發展更穩定、快速及可測試大量奈米微粒樣品的篩選平台。今年度的計劃延續以此細胞連續及即時生長分析儀為細胞毒性篩選平台,進行不同粒徑之奈米金溶液,對數種不同細胞株之細胞毒性動態影響,並建立奈米金暴露之生物分子標記。綜合我們所產出的結果,發現奈米金溶液有效抑制細胞的生長,並呈現濃度相關性,但會因細胞株不同而有不同程度的抑制效果,且其所引發之細胞毒性的機制,會因細胞株不同而不同,如在AGS細胞中,奈米金藉由引發細胞凋亡而產生細胞生長抑制;在A549細胞中,奈米金引發細胞週期停滯,進而抑制細胞的生長;而在 MRC細胞中,奈米金則可能引起細胞中刺激存活的防衛機制。進一步的,本團隊也藉由細胞暴露於不同濃度或不同粒徑之奈米金下,或是使用不同的細胞株,以DNA microarray 分析找出幾個重要的生物分子標誌,這些特定蛋白分子明顯與基因損壞及細胞週期調控機制有重要的關係,並使用Real-time PCR即時聚合酶連鎖反應確認這些生物分子標誌的表現,是由於奈米金之暴露。研究中使用的奈米金為市售之純奈米金,實驗使用濃度為因應實驗需求直接強迫細胞暴露,與一般人體可能的暴露情況完全不同,目前無法以現有的研究結果反推人體暴露劑量與可能產生之立即毒性;因此本計劃的目的旨在建立細胞毒性評估工具與平台,而非依據有限之研究成果推論人體可能之暴露劑量與毒性反應。
中文關鍵字 奈米金微粒,細胞毒性,生物標記

基本資訊

專案計畫編號 EPA-102-1605-02-01 經費年度 102 計畫經費 2700 千元
專案開始日期 2013/02/18 專案結束日期 2013/12/31 專案主持人 闕斌如
主辦單位 環檢所 承辦人 許令宜 執行單位 國立中興大學

成果下載

類型 檔名 檔案大小 說明
期末報告 EPA10216050201.pdf 8MB

Establishment of in vitro cytotoxicity assessment and molecular signature of gold nanoparticle expos

英文摘要 Nanomaterials have received considerable recent attention because of their unique properties and diverse applications in technology and life sciences. However, the nano-structures of these materials possess very different physical and chemical properties compared to their larger size counterparts. Given the increasing use of nanoparticles in a range of products, it has become crucial to develop a fundamental understanding of the biological effects of nanoparticle exposure. Many in vitro studies have suggested that nanoparticles are cytotoxic and genotoxic; however, results are inconsistent, mainly due to interference between nanoparticles and dye molecules commonly used in traditional cytotoxicity assays. The purpose of this study was to set up a systematic method for evaluating biological effects of nanogold utilizing the xCELLigence System, an electrical impedance-based, dye-free, real-time system, to continuously monitor the dynamic effects of nanogold on cell growth, additionally, in the hope of establishing a biomarker signature that is relatively specific to gold nanoparticle exposure. The inhibitory effects of nanogold on the growth of numerous cell lines demonstrated using this system were also supported by several traditional in vitro toxicity assays, including MTS, trypan blue exclusion, colony forming assays. Mechanistic studies revealed that the action of nanogold is mediated by apoptosis induction or cell cycle delay, depending on cell type and cellular context and concentration of nanogold. Additional evidence is provided from our DNA microarray analysis suggesting that many proteins involved in DNA damage responses and cell cycle regulation are significantly up-regulated or down-regulated. In this study, we present a comprehensive overview of AuNP-induced cytotoxicity in a variety of mammalian cell lines, comparing several cytotoxicity assays. Collectively, these assays offer convincing evidence of the cytotoxicity of AuNPs and support the value of a systematic approach for analyzing the toxicology of nanoparticles. We performed a comprehensive gene expression profiles following exposure to AuNPs showed significant increase in the expression of approximately of 1500 genes (fold change >2; P <0.05), compared to the control group. The results presented in this study should provide helpful guidance on the future use of gold nanoparticles in occupational and medical applications.
英文關鍵字 Gold nanoparticles, cytotoxicity, biomarkers