Eldredge C, Merritt S, Goyal M, Kulaga H, Kindt T J, Wiggins R
Department of Internal Medicine, University of Michigan, Ann Arbor.
Am J Pathol. 1991 Nov;139(5):1021-35.
The major interacting components of the immune system, major histocompatibility complex (MHC) class I and class II proteins and T cells were analyzed in a model of anti-GBM (glomerular basement membrane) disease in the rabbit that progresses to develop cellular crescents and glomerular and interstitial fibrosis. Class I and II mRNA and protein were measured in isolated glomeruli and whole renal cortex using cDNA probes and monoclonal antibodies. The distribution of T cells and class I and II proteins was assessed by immunofluorescence. Normal glomeruli contained no T cells and were class II negative. By day 4, glomeruli contained MHC class I and II mRNA and protein and class II positive T cells. Although some animals had T cells in the periglomerular area, these cells were class II negative. By day 7 periglomerular T cells were largely class II positive (activated) and there was increased MHC class I and II mRNA and protein in whole renal cortex. Later T cells accumulated in the tubulo-interstitial compartment, which became diffusely positive for MHC classes I and II, but to a variable extent in different animals. Those with high class II mRNA expression also had detectable T cell antigen receptor mRNA by Northern analysis. The authors conclude 1) in this model there was a close association between mRNA abundance and protein expression for both MHC classes I and II in glomeruli and renal cortex as a whole; 2) in this model of glomerular injury there are three phases of activation. The first phase takes place in the glomerulus and is associated with accumulation of activated T cells and MHC class I and II protein in the glomerulus. Phase 2 is associated with the accumulation of periglomerular T cells and their becoming class II positive. There is subsequent dissemination (phase 3) of activated T cells and accumulation of class I and II mRNA and protein throughout the interstitial compartment. This spacial progression of glomerulocentric inflammation is likely associated with degree of injury and permanent loss of renal function.
在兔抗肾小球基底膜(GBM)疾病模型中,对免疫系统的主要相互作用成分,即主要组织相容性复合体(MHC)I类和II类蛋白以及T细胞进行了分析,该模型会进展为细胞性新月体形成以及肾小球和间质纤维化。使用cDNA探针和单克隆抗体,在分离的肾小球和整个肾皮质中测量I类和II类mRNA及蛋白。通过免疫荧光评估T细胞以及I类和II类蛋白的分布。正常肾小球不含T细胞,且II类阴性。到第4天,肾小球含有MHC I类和II类mRNA及蛋白以及II类阳性T细胞。尽管一些动物的肾小球周围区域有T细胞,但这些细胞II类阴性。到第7天,肾小球周围T细胞大多为II类阳性(活化),且整个肾皮质中MHC I类和II类mRNA及蛋白增加。随后T细胞在肾小管间质区积聚,该区对MHC I类和II类呈弥漫性阳性,但在不同动物中的程度有所不同。通过Northern分析,那些II类mRNA表达高的动物也可检测到T细胞抗原受体mRNA。作者得出结论:1)在该模型中,肾小球和整个肾皮质中MHC I类和II类的mRNA丰度与蛋白表达之间存在密切关联;2)在该肾小球损伤模型中有三个激活阶段。第一阶段发生在肾小球,与活化T细胞以及肾小球中MHC I类和II类蛋白的积聚有关。第二阶段与肾小球周围T细胞的积聚及其变为II类阳性有关。随后活化T细胞扩散(第三阶段),I类和II类mRNA及蛋白在整个间质区积聚。这种以肾小球为中心的炎症的空间进展可能与损伤程度和肾功能的永久性丧失有关。