学术报告：New paradigms of nanoparticle effects on endothelial and epithelial cells
报告题目：New paradigms of nanoparticle effects on endothelial and epithelial cells
报 告 人：Dr. Leong（National University of Singapore）
报告时间：2014年6月24日（星期二）上午10：30
报告地点：嘉定园区学术活动中心多功能厅
报告简介：
Nanoparticles regardless as subjects of nanotoxicity or nanomedicine studies will inevitably interact with endothelial and epithelial cells. In the case of nanomedicine, while these cells are usually not the intended target, nanoparticles first interact with them. It is therefore important to understand the effects of these nanoparticles on these cells. Using generic and commonly found non-decorated nanomaterials like TiO2, silica, silver, ZnO, hydroxyapatite nanoparticles, we discovered interesting new effects and solved their mechanisms. We discovered that nanoparticles can cause endothelial leakiness (NanoEL) in vitro and in vivo by finding its way into the spaces (adherens junctions) between endothelial cells, disrupts the homophillic interactions of VE-Cadherin and trigger the signaling pathway that leads to micron sized gaps between endothelial cells (Setyawati et al. Nature Comms 2013). We also discovered that nanoparticles can inhibit cell migration by targeting and disrupting microtubules. This increases focal adhesion at the interface of surfaces and transmit to increased cell traction (Tay et al. Nano Letts 2014). We also showed that oxidative stress inducing nanoparticles can be exploited to target cancer cells while sparing normal cells via an vulnerability in p53 defective/deficient cancer cells. Functional p53 pathway in normal cells protect them against the oxidative stress of nanoparticles while cells with deficiencies in the p53 pathway succumb to oxidative stress. This is the first time where targetness of a nanomedicine is purely from a genetic difference between cancer and noncancer cells (Setyawati et al. Biomaterials 2013). This talk will also discuss about implications of these novel observations to nanotoxicity and nanomedicine.
报告人简介：
Dr. Leong graduated with a Bachelor of Chemical Engineering and a PhD in Biology from the National University of Singapore. He did his postdoctoral training in the Howard Hughes Medical Institute, University of Pennsylvania and return to his alma mater as a Lee Kuan Yew Postdoctoral Fellow. He later joined the Department of Chemical and Biomolecular Engineering at National University of Singapore as an Assistant Professor in late 2010. His research interests includes figuring out biological mechanisms of nanomaterials, nanotoxicology, new biosensors and new nanomedicine.
link: https://www.dropbox.com/s/sg6yxedifbaqs41/Talk%20Fan%20Chunhai.docx
报 告 人：Dr. Leong（National University of Singapore）
报告时间：2014年6月24日（星期二）上午10：30
报告地点：嘉定园区学术活动中心多功能厅
报告简介：
Nanoparticles regardless as subjects of nanotoxicity or nanomedicine studies will inevitably interact with endothelial and epithelial cells. In the case of nanomedicine, while these cells are usually not the intended target, nanoparticles first interact with them. It is therefore important to understand the effects of these nanoparticles on these cells. Using generic and commonly found non-decorated nanomaterials like TiO2, silica, silver, ZnO, hydroxyapatite nanoparticles, we discovered interesting new effects and solved their mechanisms. We discovered that nanoparticles can cause endothelial leakiness (NanoEL) in vitro and in vivo by finding its way into the spaces (adherens junctions) between endothelial cells, disrupts the homophillic interactions of VE-Cadherin and trigger the signaling pathway that leads to micron sized gaps between endothelial cells (Setyawati et al. Nature Comms 2013). We also discovered that nanoparticles can inhibit cell migration by targeting and disrupting microtubules. This increases focal adhesion at the interface of surfaces and transmit to increased cell traction (Tay et al. Nano Letts 2014). We also showed that oxidative stress inducing nanoparticles can be exploited to target cancer cells while sparing normal cells via an vulnerability in p53 defective/deficient cancer cells. Functional p53 pathway in normal cells protect them against the oxidative stress of nanoparticles while cells with deficiencies in the p53 pathway succumb to oxidative stress. This is the first time where targetness of a nanomedicine is purely from a genetic difference between cancer and noncancer cells (Setyawati et al. Biomaterials 2013). This talk will also discuss about implications of these novel observations to nanotoxicity and nanomedicine.
报告人简介：
Dr. Leong graduated with a Bachelor of Chemical Engineering and a PhD in Biology from the National University of Singapore. He did his postdoctoral training in the Howard Hughes Medical Institute, University of Pennsylvania and return to his alma mater as a Lee Kuan Yew Postdoctoral Fellow. He later joined the Department of Chemical and Biomolecular Engineering at National University of Singapore as an Assistant Professor in late 2010. His research interests includes figuring out biological mechanisms of nanomaterials, nanotoxicology, new biosensors and new nanomedicine.
link: https://www.dropbox.com/s/sg6yxedifbaqs41/Talk%20Fan%20Chunhai.docx
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