Grandaliano G, Gesualdo L, Bartoli F, Ranieri E, Monno R, Leggio A, Paradies G, Caldarulo E, Infante B, Schena F P
Division of Nephrology, Department of Emergency and Transplantation University of Bari, Italy.
Kidney Int. 2000 Jul;58(1):182-92. doi: 10.1046/j.1523-1755.2000.00153.x.
Obstructive nephropathy is characterized at the histologic level by tubular atrophy and interstitial monocyte infiltration. The molecular mechanisms underlying these histologic changes are still poorly defined. Epidermal growth factor (EGF) produced by tubular cells seems to play a pivotal role in the modulation of tubular cell growth, while monocyte chemotactic peptide-1 (MCP-1) is a powerful and specific chemotactic and activating factor for monocytes.
Twenty-four patients with congenital ureteropelvic junction obstruction [UPJO; 10 with recurrent urinary tract infection (UTI) and 10 with no UTI] and 15 healthy children were studied. Diagnosis was made by renal ultrasound, intravenous pielography, and MAG3 scan. Urinary samples were collected before and after surgery. In 10 patients, urine was also collected directly from the affected pelvis at the time of surgery. Urinary EGF and MCP-1 levels were measured by enzyme-linked immunosorbent assay. MCP-1 and EGF gene expression were evaluated by in situ hybridization in 15 biopsies from congenital UPJO and in 10 normal kidneys.
In normal kidneys, there was a high expression of EGF mRNA, whereas MCP-1 mRNA was undetectable. MCP-1 gene expression was strikingly increased at the tubulointerstitial level in UPJO biopsies compared with controls and was directly correlated with the extent of monocyte infiltration. In addition, UPJO kidney sections showed a marked reduction in EGF gene expression that was directly correlated with the degree of tubular damage. EGF urine concentration was significantly reduced in UPJO when compared with control and directly correlated with its renal gene expression. On the other hand, the MCP-1 urine concentration was strikingly increased in UPJO patients. It is noteworthy that a significant and inverse correlation was observed between the MCP-1 concentration in the urine collected from the obstructed pelvis and the MAG3 clearance of the obstructed kidney (r = -0.76). The presence of recurrent UTI was associated with a significantly higher MCP-1 excretion and a slight reduction in EGF urine concentration. The surgical correction of UPJO was followed by an improvement of renal function together with a significant reduction in MCP-1 excretion and a marked increase in EGF urine concentrations. Interestingly, EGF urine concentration measured before surgery was significantly correlated with the difference between the MAG3 clearance of the obstructed kidney before and after surgery.
MCP-1 and EGF seem to be involved in the pathogenesis of tubulointerstitial damage in congenital obstructive nephropathy, and their urine excretion may represent a powerful prognostic marker in this form of renal disease.
梗阻性肾病在组织学水平上的特征为肾小管萎缩和间质单核细胞浸润。这些组织学改变背后的分子机制仍未明确。肾小管细胞产生的表皮生长因子(EGF)似乎在调节肾小管细胞生长中起关键作用,而单核细胞趋化蛋白-1(MCP-1)是一种强大且特异性的单核细胞趋化和激活因子。
对24例先天性肾盂输尿管连接部梗阻(UPJO)患者[10例有复发性尿路感染(UTI),10例无UTI]和15名健康儿童进行研究。通过肾脏超声、静脉肾盂造影和MAG3扫描进行诊断。在手术前后收集尿液样本。在10例患者中,还在手术时直接从患侧肾盂收集尿液。通过酶联免疫吸附测定法测量尿液中EGF和MCP-1水平。通过原位杂交评估15例先天性UPJO活检组织和10例正常肾脏中MCP-1和EGF基因表达。
在正常肾脏中,EGF mRNA表达较高,而MCP-1 mRNA检测不到。与对照组相比,UPJO活检组织中肾小管间质水平的MCP-1基因表达显著增加,且与单核细胞浸润程度直接相关。此外,UPJO肾脏切片显示EGF基因表达明显降低,且与肾小管损伤程度直接相关。与对照组相比,UPJO患者尿液中EGF浓度显著降低,且与其肾脏基因表达直接相关。另一方面,UPJO患者尿液中MCP-1浓度显著升高。值得注意的是,从梗阻肾盂收集的尿液中MCP-1浓度与梗阻肾脏的MAG3清除率之间存在显著负相关(r = -0.76)。复发性UTI的存在与MCP-1排泄显著增加和尿液中EGF浓度略有降低有关。UPJO手术矫正后,肾功能改善,同时MCP-1排泄显著减少,尿液中EGF浓度显著增加。有趣的是,术前测量的尿液中EGF浓度与梗阻肾脏术前和术后MAG3清除率的差异显著相关。
MCP-1和EGF似乎参与了先天性梗阻性肾病肾小管间质损伤的发病机制,它们的尿液排泄可能是这种形式肾病的有力预后标志物。