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正常大鼠及链脲佐菌素诱导的糖尿病大鼠血浆中丙二醛修饰蛋白及其抗体

Malondialdehyde modified proteins and their antibodies in the plasma of control and streptozotocin induced diabetic rats.

作者信息

Lung C C, Pinnas J L, Yahya M D, Meinke G C, Mooradian A D

机构信息

Department of Microbiology and Immunology, University of Arizona Health Science Center, Tucson 85724.

出版信息

Life Sci. 1993;52(3):329-37. doi: 10.1016/0024-3205(93)90225-r.

Abstract

One of the possible mechanisms of diabetes-related tissue damage is modification of various proteins via lipid peroxidation byproducts such as malondialdehyde (MDA). To determine the extent of MDA derivatization of plasma proteins, Western blots were carried out using anti-MDA antisera to study plasma proteins in control and streptozotocin (STZ)-induced diabetic rats. Since MDA can modify proteins and may alter or enhance their antigenicity, we screened plasma samples for anti-MDA antibodies using enzyme-linked immunosorbent assay (ELISA), and confirmed antibody specificity by inhibition ELISA. Circulating immune complexes containing MDA were also assayed. This study is the first demonstration of the existence in plasma of MDA-modified proteins with a molecular weight of approximately 100 Kd. Both control and diabetic rats have similar concentrations of plasma anti-MDA antibodies and circulating immune complexes. These results do not support the notion that diabetes alters the immune response to MDA modified proteins. Whether MDA modification of proteins participate in immunological processes that lead to tissue injury remains to be demonstrated.

摘要

糖尿病相关组织损伤的一种可能机制是通过脂质过氧化副产物(如丙二醛,MDA)对各种蛋白质进行修饰。为了确定血浆蛋白的MDA衍生化程度,使用抗MDA抗血清进行蛋白质印迹分析,以研究对照大鼠和链脲佐菌素(STZ)诱导的糖尿病大鼠的血浆蛋白。由于MDA可以修饰蛋白质并可能改变或增强其抗原性,我们使用酶联免疫吸附测定(ELISA)筛选血浆样本中的抗MDA抗体,并通过抑制ELISA确认抗体特异性。还检测了含有MDA的循环免疫复合物。本研究首次证明血浆中存在分子量约为100 Kd的MDA修饰蛋白。对照大鼠和糖尿病大鼠的血浆抗MDA抗体浓度和循环免疫复合物浓度相似。这些结果不支持糖尿病会改变对MDA修饰蛋白的免疫反应这一观点。蛋白质的MDA修饰是否参与导致组织损伤的免疫过程仍有待证明。

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