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Probing energy metabolism and microviscosity in cancer using FLIM

机译:使用FLIM探测癌症中的能量代谢和微粘度

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Fluorescence lifetime imaging microscopy (FLIM) is a promising non-invasive highly sensitive technique for probing multiple physiological and physicochemical parameters in living cells and tissues. The present study is focused on the investigation of bioenergetics and microscopic viscosity of cultured cancer cells and animal tumors using FLIM during natural growth and chemotherapy. Fluorescence lifetime measurements of the metabolic cofactor NAD(P)H revealed a decrease of the relative amplitude of free NAD(P)H after cisplatin treatment, indicating a change towards a more oxidative metabolic state. Microviscosity mapping performed with the use of fluorescent molecular rotor BODIPY-2 showed a pronounced increase in the plasma membrane viscosity in cancer cells exposed to cisplatin. Although biochemical mechanisms underlying the metabolic and viscosity alterations during chemotherapy have yet to be clarified, our data suggest that the cisplatin-induced changes in cellular metabolism and membrane viscosity play a role in the cytotoxicity of the drug. The results of the study contribute to an understanding of mechanisms of cisplatin action and will be useful for development new approach for assessing response to a therapy.
机译:荧光寿命成像显微镜(FLIM)是一种有前途的非侵入性高灵敏度技术,用于探测活细胞和组织中的多个生理和理化参数。本研究的重点是在自然生长和化学疗法中使用FLIM研究培养的癌细胞和动物肿瘤的生物能和微观粘度。代谢辅因子NAD(P)H的荧光寿命测量结果显示,顺铂处理后游离NAD(P)H的相对幅度降低,表明其向更氧化的代谢状态转变。使用荧光分子转子BODIPY-2进行的微粘度测绘显示,暴露于顺铂的癌细胞中质膜粘度显着增加。尽管尚不清楚化学疗法中代谢和粘度改变的潜在生化机制,但我们的数据表明顺铂诱导的细胞代谢和膜粘度变化在药物的细胞毒性中起作用。该研究结果有助于人们了解顺铂作用机制,并将有助于开发一种评估疗法反应的新方法。

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