Schmidt-Glenewinkel Hannah, Reinz Eileen, Eils Roland, Brady Nathan R
From the Division of Theoretical Bioinformatics, 69120 Heidelberg, Germany.
Infection and Cancer Research Program, German Cancer Research Center, 69120 Heidelberg, Germany.
J Biol Chem. 2009 Jun 19;284(25):17243-17252. doi: 10.1074/jbc.M809586200. Epub 2009 Mar 17.
Epidermal growth factor (EGF) receptor (EGFR) overexpression is a hallmark of many cancers. EGFR endocytosis is a critical step in signal attenuation, raising the question of how receptor expression levels affect the internalization process. Here we combined quantitative experimental and mathematical modeling approaches to investigate the role of the EGFR expression level on the rate of receptor internalization. Using tetramethylrhodamine-labeled EGF, we established assays for quantifying EGF-triggered EGFR internalization by both high resolution confocal microscopy and flow cytometry. We determined that the flow cytometry approach was more sensitive for examining large populations of cells. Mathematical modeling was used to investigate the relationship between EGF internalization kinetics, EGFR expression, and internalization machinery. We predicted that the standard parameter used to assess internalization kinetics, the temporal evolution r(t) of the ratio of internalized versus surface-located ligand.receptor complexes, does not describe a straight line, as proposed previously. Instead, a convex or concave curve occurs depending on whether initial receptor numbers or internalization adaptors are limiting the uptake reaction, respectively. To test model predictions, we measured EGF-EGFR binding and internalization in cells expressing different levels of green fluorescent protein-EGFR. As expected, surface binding of rhodamine-labeled EGF increased with green fluorescent protein-EGFR expression level. Unexpectedly, internalization of ligand. receptor complexes increased linearly with increasing receptor expression level, suggesting that receptors and not internalization adaptors were limiting the uptake in our experimental model. Finally, determining the ratio of internalized versus surface-located ligand.receptor complexes for this cell line confirmed that it follows a convex curve, supporting our model predictions.
表皮生长因子(EGF)受体(EGFR)的过表达是许多癌症的一个标志。EGFR内吞作用是信号衰减的关键步骤,这就引发了一个问题,即受体表达水平如何影响内化过程。在这里,我们结合了定量实验和数学建模方法,以研究EGFR表达水平对受体内化速率的作用。使用四甲基罗丹明标记的EGF,我们通过高分辨率共聚焦显微镜和流式细胞术建立了定量EGF触发的EGFR内吞作用的检测方法。我们确定流式细胞术方法在检测大量细胞时更敏感。数学建模用于研究EGF内化动力学、EGFR表达和内化机制之间的关系。我们预测,用于评估内化动力学的标准参数,即内化的与位于表面的配体-受体复合物比例的时间演变r(t),并不像之前所提出的那样描述一条直线。相反,根据初始受体数量或内化衔接子是否分别限制摄取反应,会出现凸曲线或凹曲线。为了验证模型预测,我们测量了表达不同水平绿色荧光蛋白-EGFR的细胞中EGF-EGFR的结合和内化。正如预期的那样,罗丹明标记的EGF的表面结合随着绿色荧光蛋白-EGFR表达水平的增加而增加。出乎意料的是,配体-受体复合物的内化随着受体表达水平的增加而线性增加,这表明在我们的实验模型中,限制摄取的是受体而不是内化衔接子。最后,确定该细胞系内化的与位于表面的配体-受体复合物的比例证实它遵循凸曲线,支持了我们的模型预测。