Sado Y, Kagawa M, Naito I, Okigaki T
Division of Immunology, Shigei Medical Research Institute, Okayama, Japan.
Virchows Arch B Cell Pathol Incl Mol Pathol. 1991;60(5):345-51. doi: 10.1007/BF02899566.
The nephritogenic antigen that induces antiglomerular basement membrane antibody-induced glomerulonephritis (anti-GBM nephritis) in rats was isolated from collagenase-solubilized bovine renal basement membranes. Purification was achieved using antibody-coupled affinity columns which were originally used for the purification of trypsin-solubilized nephritogenic antigen (Sado et al. 1984a). The nephritogenic antigen was a heteropolymer composed of P2 (Mr 28 kDa) and P3 (Mr 30 kDa) polypeptides as monomers and their dimers in sodium-dodecyl-sulfate (SDS) polyacrylamide gel electrophoresis. The P3 polypeptide was considered to be the nephritogenic epitope, since a fraction composed of the P2 polypeptide alone was not nephritogenic. The properties of the nephritogenic epitope were the same as those of the Goodpasture epitope (M2*), which is a noncollagenous domain of the alpha 3 chain of type IV collagen (Butkowski et al. 1985; Saus et al. 1988), indicating that the nephritogenic antigen is the same as the Goodpasture antigen.
从胶原酶溶解的牛肾基底膜中分离出了能在大鼠中诱导抗肾小球基底膜抗体介导的肾小球肾炎(抗GBM肾炎)的致肾炎抗原。使用最初用于纯化胰蛋白酶溶解的致肾炎抗原的抗体偶联亲和柱进行纯化(佐渡等人,1984年a)。在十二烷基硫酸钠(SDS)聚丙烯酰胺凝胶电泳中,致肾炎抗原是一种由P2(分子量28 kDa)和P3(分子量30 kDa)多肽作为单体及其二聚体组成的杂聚物。P3多肽被认为是致肾炎表位,因为仅由P2多肽组成的部分没有致肾炎性。致肾炎表位的特性与Goodpasture表位(M2*)相同,后者是IV型胶原α3链的非胶原结构域(布特科夫斯基等人,1985年;索斯等人,1988年),这表明致肾炎抗原与Goodpasture抗原相同。