摘要: 目的 探讨原发性肾病综合征(PNS)患儿肾组织核因子-κB(NF-κB)活化水平及其与肾组织病理类型、24h尿蛋白定量的关系。方法 2002年2月至2004年9月,收集山东大学齐鲁医院小儿内科51例PNS患儿活检肾组织及5例肾脏手术切除的正常肾组织。采用免疫组织化学染色法及多媒体彩色病理图文分析系统MPIAS-500,观察PNS患儿各病理类型肾组织及正常肾组织NF-κB的活化水平,同期收集PNS患儿24h尿蛋白定量。结果 微小病变型(MCD)、非微小病变型(NMCD)PNS患儿肾小球及肾小管中NF-κB活化水平均较对照组显著增强;NMCD患儿肾小球及肾小管中NF-κB的表达水平显著高于MCD患儿;20例系膜增殖性肾小球肾炎(MsPGN)患儿肾组织NF-κB活化水平随系膜增殖程度加重而增高;PNS患儿肾小球及肾小管NF-κB表达水平与24h尿蛋白定量呈显著正相关。结论PNS患儿肾小球及肾小管中NF-κB活化水平上调,且与组织病理类型、尿蛋白量相关,NF-κB的异常活化在PNS发病中起重要作用。
Abstract Objective To study activation of transcription factor NFKappa B(NF-κB) and its role in regulating the expression of inflammatory mediators involved in pathogenesis of primary nephrotic syndrome (PNS).
Methods To explore the role of NF-κB in the pathogenesis of PNS in children,and its significance for pathological changes as well as 24hour urine protein excretion,we examined NF-κB activity in glomeruli and tubular tissues by twostep immunohistochemical staining from the kidney biopsy specimen of 51 children with PNS,and from 5 patients after renal operation.
Results We found that NF-κB activity significantly increased both in MCD and NMCD children compared with the controls,and the activation of NF-κB in MCD was different from that of NMCD;there was also statistical difference of NF-κB activity between mild,moderate,severe MsPGN and the controls Additionally,positive correlation was observed between NF-κB activity of glomeruli and renal tubules and 24hour urine protein excretion.
Conclusion These results suggested that the upregulated activation of NF-κB in glomerular and tubular tissues of children with PNS is related to severity,pathological changes and urine protein excretion,and involved in the pathogenesis of PNS.
Key words Nuclear factor kappa B;Primary nephrotic syndrome;Pathology;Children
赵红洋,孙若鹏,甄军晖,董俊华. 原发性肾病综合征患儿肾组织核因子-κB活化水平与病理类型及尿蛋白关系[J]. 中国实用儿科杂志.
Zhao Hongyang,Sun Ruopeng,Zhen Junhui et al.. The activation of nuclear factorKappa B in kidney tissue in children with primary nephrotic syndrome and its relationship with pathological changes and urine protein excretion.[J]. .