Orlando R A, Farquhar M G
Division of Cellular and Molecular Medicine, University of California, San Diego, La Jolla 92093.
Proc Natl Acad Sci U S A. 1993 May 1;90(9):4082-6. doi: 10.1073/pnas.90.9.4082.
gp330 is a large glycoprotein located in clathrin-coated pits at the surface of the glomerular and proximal tubule epithelia in the rat kidney. It was originally identified as the target of autoimmune antibodies in Heymann nephritis (HN) and has since been shown to be a member of the low density lipoprotein receptor gene family and to form a stable association with receptor-associated protein (RAP), which together constitute the HN antigen complex (HNAC). Progress in defining the normal functions of gp330 as well as the molecular mechanisms of HN has been hampered by the lack of an available kidney cell line that expresses this protein. We here report the identification of a rat yolk sac carcinoma cell line (L2) that synthesizes HNAC and expresses it in coated pits at the cell surface. gp330 and RAP from L2 cells are immunologically identical to their kidney counterparts, and peptide maps of gp330 yielded identical peptide fragments. Characterization of the cell line revealed that there are 3.3 x 10(4) gp330 molecules per L2 cell and that the cells produce a soluble form of gp330 that is released into the medium. Heparin ligand blot analysis demonstrated that RAP but not gp330 binds heparin. By heparin affinity chromatography, gp330 and RAP copurify, indicating that the glycosaminoglycan binding site within RAP is accessible when the subunit is complexed with gp330. These results indicate that the L2 cell line provides a valid and useful model for studies on the function of HNAC and the pathogenesis of HN.
gp330是一种大型糖蛋白,位于大鼠肾脏肾小球和近端肾小管上皮细胞表面的网格蛋白包被小窝中。它最初被鉴定为海曼肾炎(HN)中自身免疫抗体的靶标,此后已被证明是低密度脂蛋白受体基因家族的成员,并与受体相关蛋白(RAP)形成稳定的结合,二者共同构成HN抗原复合物(HNAC)。由于缺乏表达这种蛋白的可用肾细胞系,在确定gp330的正常功能以及HN的分子机制方面的进展受到了阻碍。我们在此报告鉴定出一种大鼠卵黄囊癌细胞系(L2),该细胞系合成HNAC并在细胞表面的包被小窝中表达。L2细胞中的gp330和RAP与它们在肾脏中的对应物在免疫上相同,并且gp330的肽图产生了相同的肽片段。对该细胞系的表征显示,每个L2细胞有3.3×10⁴个gp330分子,并且这些细胞产生一种可溶形式的gp330,其被释放到培养基中。肝素配体印迹分析表明RAP而非gp330结合肝素。通过肝素亲和层析,gp330和RAP共同纯化,表明当亚基与gp330复合时,RAP内的糖胺聚糖结合位点是可及的。这些结果表明,L2细胞系为研究HNAC的功能和HN的发病机制提供了一个有效的有用模型。