Merker M P, Carley W W, Gillis C N
Department of Anesthesiology, Yale University School of Medicine, New Haven, Connecticut 06510.
FASEB J. 1990 Sep;4(12):3040-8. doi: 10.1096/fasebj.4.12.2168327.
To study the biochemical characteristics of endothelium in vivo, we radioiodinated endothelial membrane proteins of the perfused rabbit lung using a water soluble analog of the Bolton-Hunter reagent, 125I-sulfosuccinimidyl (hydroxyphenyl) propionate (125I-s-SHPP). This technique led to a 10-fold increase in specific activity of radioiodinated lung membrane protein compared with our previously reported method using lactoperoxidase and glucose oxidase-catalyzed radioiodination. Tissue autoradiography confirmed that radioiodination was largely confined to the endothelium. Perfusion pressure, wet-to-dry weight ratios, and the morphological appearance of the lungs were within normal limits, indicating that the procedure does not cause apparent lung injury. Lectin binding to a crude membrane fraction of 125I-s-SHPP labeled lung led to isolation of several putative endothelial membrane proteins. Immunoprecipitation studies with appropriate antibodies enabled the identification of radioiodinated angiotensin-converting enzyme and beta 2-microglobulin associated major histocompatibility complex class I molecules in the membrane fraction. This technique will be useful for studying biochemical responses of the endothelium in vivo to a variety of pharmacological and physiology stimuli.
为了研究体内内皮细胞的生化特性,我们使用博尔顿-亨特试剂的水溶性类似物125I-磺基琥珀酰亚胺(羟苯基)丙酸酯(125I-s-SHPP)对灌注兔肺的内皮细胞膜蛋白进行放射性碘化。与我们先前报道的使用乳过氧化物酶和葡萄糖氧化酶催化放射性碘化的方法相比,该技术使放射性碘化肺膜蛋白的比活性提高了10倍。组织放射自显影证实放射性碘化主要局限于内皮细胞。灌注压力、湿重与干重之比以及肺的形态外观均在正常范围内,表明该操作不会导致明显的肺损伤。凝集素与125I-s-SHPP标记肺的粗膜部分结合,从而分离出几种假定的内皮细胞膜蛋白。用适当抗体进行的免疫沉淀研究能够鉴定膜部分中放射性碘化的血管紧张素转换酶和与β2-微球蛋白相关的主要组织相容性复合体I类分子。该技术将有助于研究体内内皮细胞对各种药理和生理刺激的生化反应。