Clayman M D, Martinez-Hernandez A, Michaud L, Alper R, Mann R, Kefalides N A, Neilson E G
J Exp Med. 1985 Feb 1;161(2):290-305. doi: 10.1084/jem.161.2.290.
Using monoclonal antibody affinity chromatography, we isolated a 48,000 mol wt, glucose-rich glycoprotein (3M-1) from collagenase-solubilized rabbit renal tubular basement membrane (SRTA). The purified 3M-1 protein is noncollagenous, and is capable of inducing anti-TBM (tubular basement membrane) antibodies and interstitial nephritis in susceptible hosts. Further, when SRTA, at a normally nephritogenic dose, was selectively depleted of 3M-1, it lost its ability to induce disease. As shown by immunofluorescent techniques, 3M-1 appears to be localized on rodent TBM to the exclusion of the glomerular basement membrane, but was lacking in the TBM of the LEW rat, a strain devoid of the relevant antigen of anti-TBM disease. Immunoelectron microscopy revealed that 3M-1 was associated with the most lateral aspect of the TBM, which borders, and lies in the interstitium. These results indicate that 3M-1 is the nephritogenic antigen producing experimental anti-TBM disease.
利用单克隆抗体亲和层析法,我们从胶原酶溶解的兔肾小管基底膜(SRTA)中分离出一种分子量为48,000的富含葡萄糖的糖蛋白(3M-1)。纯化后的3M-1蛋白是非胶原性的,能够在易感宿主中诱导抗肾小管基底膜(TBM)抗体和间质性肾炎。此外,当以正常致肾炎剂量的SRTA被选择性去除3M-1后,它失去了诱导疾病的能力。免疫荧光技术显示,3M-1似乎定位于啮齿动物的TBM上,而肾小球基底膜上没有,但在LEW大鼠的TBM中缺乏,LEW大鼠是一种缺乏抗TBM疾病相关抗原的品系。免疫电子显微镜显示,3M-1与TBM最外侧部分相关,该部分与间质相邻并位于间质中。这些结果表明,3M-1是产生实验性抗TBM疾病的致肾炎抗原。