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Novel method to differentiate 3T3 L1 cells in vitro to produce highly sensitive adipocytes for a GLUT4 mediated glucose uptake using fluorescent glucose analog

机译:使用荧光葡萄糖类似物体外分化3T3 L1细胞以产生高度敏感的脂肪细胞以进行GLUT4介导的葡萄糖摄取的新方法

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摘要

Adipocytes play a vital role in glucose metabolism. 3T3 L1 pre adipocytes after differentiation to adipocytes serve as excellent in vitro models and are useful tools in understanding the glucose metabolism. The traditional approaches adopted in pre adipocyte differentiation are lengthy exercises involving the usage of IBMX and Dexamethasone. Any effort to shorten the time of differentiation and quality expression of functional differentiation in 3T3 L1 cells in terms of enhanced Insulin sensitivity has an advantage in the drug discovery process. Thus, there is a need to develop a new effective method of differentiating the pre adipocytes to adipocytes and to use such methods for developing efficacious therapeutic molecules. We observed that a combination of Dexamethasone and Troglitazone generated differentiated adipocytes over fewer days as compared to the combination of IBMX and Dexamethasone which constitutes the standard protocol followed in our laboratory. The experiments conducted to compare the quality of differentiation yielded by various differentiating agents indicated that the lipid droplet accumulation increased by 112 % and the GLUT4 mediated glucose uptake by 137 % in cells differentiated with Troglitazone and Dexamethasone than in cells differentiated traditionally. The comparative studies conducted for evaluating efficient measurable glucose uptake by GOPOD assay, radioactive 3H-2-deoxy-D-glucose assay and by non-radioactive 6-NBDG (fluorescent analog of glucose) indicated that the non-radioactive method using 6-NBDG showed a higher signal to noise ratio than the conventional indirect glucose uptake method (GOPOD assay) and the radioactive 3H-2-deoxy-D-glucose uptake method. Differentiated 3T3 L1 cells when triggered with 2.5 ng/mL of Insulin showed 3.3 fold more glucose uptake in non-radioactive method over the radioactive 3H-2-deoxy-D-glucose uptake method. The results of this study have suggested that a combination of Dexamethasone and Troglitazone for 3T3 L1 cell differentiation helps in better quality differentiation over a short period of time with increased sensitivity to Insulin. The application of these findings for developing new methods of screening novel Insulin mimetics and for evaluating the immunological responses has been discussed.
机译:脂肪细胞在葡萄糖代谢中起着至关重要的作用。分化为脂肪细胞后的3T3 L1前脂肪细胞可作为出色的体外模型,并且是了解葡萄糖代谢的有用工具。脂肪细胞分化前采用的传统方法是冗长的练习,涉及使用IBMX和地塞米松。就提高胰岛素敏感性而言,任何缩短3T3 L1细胞分化时间和功能分化质量表达的努力在药物发现过程中均具有优势。因此,需要开发一种新的将前脂肪细胞分化为脂肪细胞的有效方法,并使用这种方法来开发有效的治疗分子。我们观察到,与IBMX和地塞米松的组合相比,地塞米松和曲格列酮的组合在几天内生成了分化的脂肪细胞,构成了我们实验室遵循的标准方案。实验比较了各种分化剂产生的分化质量,结果表明,与传统分化细胞相比,曲格列酮和地塞米松分化的细胞脂质滴积累增加112%,GLUT4介导的葡萄糖摄取增加137%。通过GOPOD分析,放射性 3 H-2-脱氧-D-葡萄糖分析和非放射性6-NBDG(葡萄糖的荧光类似物)评估有效测量的葡萄糖摄取的比较研究表明,使用6-NBDG的非放射性方法显示出比常规间接葡萄糖摄取方法(GOPOD分析)和放射性 3 H-2-脱氧-D-葡萄糖摄取方法更高的信噪比。当用2.5ng / mL胰岛素触发时,分化的3T3 L1细胞在非放射性方法中的葡萄糖摄取量是放射性 3 H-2-deoxy-D-葡萄糖摄取方法的3.3倍。这项研究的结果表明,地塞米松和曲格列酮的组合可用于3T3 L1细胞分化,有助于在短时间内更好地进行质量分化,同时提高对胰岛素的敏感性。讨论了这些发现在开发筛选新型胰岛素模拟物和评估免疫反应的新方法中的应用。

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