Chatterjee Saurabh, Premachandran Sudha, Bagewadikar R S, Poduval T B
Immunology and Hyperthermia Section, Radiation Biology and Health Sciences Division, Bhabha Atomic Research Centre, Trombay, Mumbai-400 085, India.
Radiat Res. 2005 Mar;163(3):351-5. doi: 10.1667/rr3313.
A new assay has been developed to study the osmotic fragility of red blood cells (RBCs) and the involvement of oxygen-derived free radicals and other oxidant species in causing human red blood cell hemolysis. The amount of hemoglobin released into the supernatant, which is a measure of human red blood cell hemolysis, is monitored using an ELISA reader. This ELISA-based osmotic fragility test compared well with the established osmotic fragility test, with the added advantage of significantly reduced time and the requirement of only 60 mul of blood. This small amount of blood was collected fresh by finger puncture and was immediately diluted 50 times with PBS, thus eliminating the use of anticoagulants and the subsequent washings. Since exposure of RBCs to 400 Gy gamma radiation caused less than 5% hemolysis 24 h after irradiation, the RBC hemolysis induced by gamma radiation was amplified by irradiating the cell in hypotonic saline. The method was validated by examining the protective effect of Trolox, an analog of vitamin E and reduced glutathione (GSH), a well-known radioprotector, against human RBC hemolysis caused by the combined action of radiation and osmotic stress. Trolox, a known membrane stabilizer and an antioxidant, and GSH offered significant protection. This new method, which is simple and requires significantly less time and fewer RBCs, may offer the ability to study the effects of antioxidants and membrane stabilizers on human red blood cell hemolysis induced by radiation and oxidative stress and assess the osmotic fragility of erythrocytes.
已开发出一种新的检测方法来研究红细胞(RBC)的渗透脆性,以及氧衍生自由基和其他氧化剂在导致人类红细胞溶血中的作用。使用酶联免疫吸附测定(ELISA)读数器监测释放到上清液中的血红蛋白量,以此作为人类红细胞溶血的指标。这种基于ELISA的渗透脆性试验与既定的渗透脆性试验相比效果良好,其额外优势是显著减少了时间,且仅需60微升血液。通过手指穿刺新鲜采集这少量血液,并立即用磷酸盐缓冲液(PBS)稀释50倍,从而无需使用抗凝剂及后续洗涤步骤。由于红细胞在400戈瑞伽马辐射照射后24小时内溶血率低于5%,因此通过在低渗盐水中照射细胞来放大伽马辐射诱导的红细胞溶血。通过检测维生素E类似物Trolox和著名的辐射防护剂还原型谷胱甘肽(GSH)对辐射和渗透应激联合作用导致的人类红细胞溶血的保护作用,验证了该方法。Trolox是一种已知的膜稳定剂和抗氧化剂,GSH提供了显著的保护作用。这种新方法简单,所需时间显著减少,且所需红细胞数量较少,可能提供研究抗氧化剂和膜稳定剂对辐射和氧化应激诱导的人类红细胞溶血的影响以及评估红细胞渗透脆性的能力。