机构地区:[1]南开大学医学院,天津300191 [2]解放军总医院第一医学中心肾脏病医学部、解放军肾脏病研究所、肾脏疾病国家重点实验室、国家慢性肾病临床医学研究中心、肾脏疾病研究北京市重点实验室,北京100853
出 处:《中华肾病研究电子杂志》2022年第1期1-6,共6页Chinese Journal of Kidney Disease Investigation(Electronic Edition)
基 金:国家重点研发计划项目(2020YFA0113004);国家自然科学基金重点项目(81830060)
摘 要:目的以人Ⅳ型胶原α3链非胶原区结构域1[α3(Ⅳ)NC1]上的线性多肽α3127-148作为抗原,建立抗肾小球基底膜(GBM)肾炎大鼠模型。方法7~8周龄雌性WKY大鼠30只,体重100~150 g,随机分为3组(10只/组):对照组、低剂量多肽免疫组(低剂量组)、高剂量多肽免疫组(高剂量组)。多肽α3127-148一次性注射于大鼠后足垫来进行建模,低剂量组注射200μg/kg、高剂量组注射300μg/kg、对照组仅注射等体积溶剂。每周定时收集24 h尿测尿蛋白浓度。所有动物在第6周末处死,检测血清肌酐和尿素氮。大鼠肾组织切片进行PAS染色、Masson染色及免疫荧光染色。结果与对照组相比,高剂量组24 h尿蛋白浓度自第3周末开始明显升高(P<0.05),第6周末血清尿素氮和肌酐水平均明显升高(P<0.05),PAS染色可见肾小球硬化、弥漫性新月体形成,荧光染色可见IgG在GBM呈明显线性沉积。与对照组比较,低剂量组第6周末24 h尿蛋白浓度明显升高(P<0.05),PAS染色亦见肾小球有明显损伤,但较高剂量组轻。结论本研究采用线性多肽α3127-148免疫WKY大鼠,成功地建立了抗GBM肾炎模型,该方法简单、效率高。Objective To establish a rat model of anti-glomerular basement membrane(GBM)glomerulonephritis induced by the linear polypeptideα3127-148 on the non-collagen domain 1 of theα3 chain of human type IV collagen[α3(IV)NC1]as the antigen.Methods Thirty female WKY rats aged 7-8 weeks,weighing 100-150 g,were randomly divided into 3 groups:the control group,the low-dose polypeptide immunization group(low-dose group),and the high-dose polypeptide immunization group(high-dose group)with 10 rats each.The polypeptideα3127-148 in the solvent was injected into the hind foot pad of rats only once for modeling.The low-dose group was injected with the polypeptideα3127-148 of 200μg/kg,the high-dose group with 300μg/kg,and the control group was injected with the solvent of the equal volume.After immunization,the 24-hour urine was collected regularly each week to measure the urine protein concentration.All the rats were sacrificed at the end of the 6 th week,and serum creatinine and blood urea nitrogen were measured.Rat kidney tissue sections were subjected to PAS staining,Masson staining,and immunofluorescence staining.Results Compared with the control group,the high-dose group showed significantly higher level of the 24-hour urine protein from the end of the 3 rd week(P<0.05),and significantly higher level of the serum urea nitrogen and creatinine at the end of the 6 th week(P<0.05),together with glomerular sclerosis and diffuse crescent formation in PAS staining,as well as GBM linear deposit of IgG in fluorescent staining.Compared with the control group at the end of the 6 th week,the low-dose group displayed higher level of 24-hour urine protein(P<0.05)and obvious damage to the glomeruli in PAS staining,but the latter was milder than that in the high-dose group.Conclusion In this study,a linear polypeptideα3127-148 was used to immunize WKY rats and an anti-GBM nephritis model was successfully established,the method of which was simple and efficient.
关 键 词:抗肾小球基底膜肾炎 新月体 线性多肽α3127-148
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