Crary G S, Katz A, Fish A J, Michael A F, Butkowski R J
Department of Pediatrics, University of Minnesota, Minneapolis.
Kidney Int. 1993 Jan;43(1):140-6. doi: 10.1038/ki.1993.23.
Tubulointerstitial nephritis antigen (TIN antigen) is a basement membrane component which is recognized by human autoantibodies in TIN and has been shown to induce TIN in Brown Norway (BN) rats. Detectable by immunofluorescent microscopy, TIN antigen reacts with monoclonal, polyclonal, and human autoantibodies in basement membranes of kidney cortex, small intestine, skin and cornea. Specific sites of TIN antigen within kidney cortex include basement membranes of proximal tubules, distal tubules, Bowman's capsule and peritubular capillaries, with highest concentration in proximal tubular basement membrane (TBM). TIN antigen is also present in interstitium between tubules and in the periarterial sheath, but not in glomerular basement membrane or mesangial matrix. Immunoblotting of TIN antigen isolated from rabbit TBM reveals a major 58 kDa component with minor components of 300 kDa, 175 kDa, 160 kDa, 100 kDa and 50 kDa. Partial protein sequence analysis indicates that 58 kDa TIN antigen represents a newly defined glycoprotein. The structural relationships between various molecular weight forms are currently being investigated. High molecular weight (HMW) forms of TIN antigen, consisting of a mixture of 300 kDa, 175 kDa and 160 kDa forms, are more efficient than low molecular weight (LMW) forms (58 kDa and 50 kDa forms) in inducing TIN in BN rats. The resultant antibody specificity of rats injected with either HMW TIN antigen or LMW TIN antigen is identical as determined by immunofluorescent microscopy and Western analysis. Higher antibody titers and greater amounts of kidney-bound IgG are found in the HMW TIN antigen-immunized animals. TIN antigen is the primary target of anti-TBM antibodies in human and experimental immunologically-mediated anti-TBM nephritis.
肾小管间质性肾炎抗原(TIN抗原)是一种基底膜成分,在肾小管间质性肾炎中可被人类自身抗体识别,并已证明可在棕色挪威(BN)大鼠中诱发肾小管间质性肾炎。通过免疫荧光显微镜可检测到,TIN抗原可与肾皮质、小肠、皮肤和角膜基底膜中的单克隆抗体、多克隆抗体及人类自身抗体发生反应。肾皮质内TIN抗原的特定部位包括近端小管、远端小管、鲍曼囊和肾小管周围毛细血管的基底膜,其中近端小管基底膜(TBM)中的浓度最高。TIN抗原也存在于小管间的间质和动脉周围鞘中,但不存在于肾小球基底膜或系膜基质中。从兔TBM中分离出的TIN抗原进行免疫印迹分析,显示主要成分是58 kDa,还有300 kDa、175 kDa、160 kDa、100 kDa和50 kDa的次要成分。部分蛋白质序列分析表明,58 kDa的TIN抗原代表一种新定义的糖蛋白。目前正在研究各种分子量形式之间的结构关系。由300 kDa、175 kDa和160 kDa形式混合而成的高分子量(HMW)形式的TIN抗原,在诱导BN大鼠发生肾小管间质性肾炎方面比低分子量(LMW)形式(58 kDa和50 kDa形式)更有效。通过免疫荧光显微镜和Western分析确定,注射HMW TIN抗原或LMW TIN抗原的大鼠产生的抗体特异性相同。在HMW TIN抗原免疫的动物中发现了更高的抗体滴度和更多与肾脏结合 的IgG。TIN抗原是人类和实验性免疫介导的抗TBM肾炎中抗TBM抗体的主要靶点。