Aguilar-Gaytan Rocio, Mas-Oliva Jaime
Instituto de Fisiología Celular, Universidad Nacional Autónoma de México, Apdo. Postal 70-243, 04510 México, D.F., Mexico.
Biochem Biophys Res Commun. 2003 Jun 6;305(3):510-7. doi: 10.1016/s0006-291x(03)00796-4.
We report the characterization of a cell system employing Chinese hamster ovary (CHO) cells and CHO cells transfected with the scavenger receptor class A (CHO-SRA) using extracellularly produced reactive oxygen species (ROS) in order to study the endocytic function of the scavenger receptor. The oxidative environment was produced using tert-butyl hydroperoxide (TBH) and characterized by flow cytometry and cell viability. Once an adequate oxidative environment was established, binding and internalization studies of radiolabeled acetylated LDL particles (125I-labeled Ac-LDL) with CHO-SRA cells were carried out. RT-PCR analysis using total RNAs from CHO-SRA cells revealed that oxidative stress does not alter the expression of the scavenger receptor. However, internalization of 125I-labeled Ac-LDL through this receptor carried out by these cells was completely abolished under extracellularly oxidative conditions. Together, these results support the idea that an oxidative stress produced extracellularly, inhibiting the endocytosis of the scavenger receptor, could help to understand and explain the mechanisms by which several physiologically important ligands are accumulated in the extracellular space with its consequent cell damage.
我们报告了一种细胞系统的特性,该系统采用中国仓鼠卵巢(CHO)细胞以及转染了A类清道夫受体的CHO细胞(CHO-SRA),利用细胞外产生的活性氧(ROS)来研究清道夫受体的内吞功能。使用叔丁基过氧化氢(TBH)产生氧化环境,并通过流式细胞术和细胞活力对其进行表征。一旦建立了适当的氧化环境,就对CHO-SRA细胞进行放射性标记的乙酰化低密度脂蛋白颗粒(125I标记的Ac-LDL)的结合和内化研究。使用来自CHO-SRA细胞的总RNA进行的RT-PCR分析表明,氧化应激不会改变清道夫受体的表达。然而,在细胞外氧化条件下,这些细胞通过该受体进行的125I标记的Ac-LDL内化完全被消除。总之,这些结果支持这样一种观点,即细胞外产生的氧化应激抑制清道夫受体的内吞作用,这有助于理解和解释几种生理上重要的配体在细胞外空间积累并导致细胞损伤的机制。