Shimizu Masaki, Ohta Kazuhide, Yang Yonghong, Nakai Akiko, Toma Tomoko, Saikawa Yutaka, Kasahara Yoshihito, Yachie Akihiro, Yokoyama Hitoshi, Seki Hidetoshi, Koizumi Shoichi
Department of Pediatrics, Graduate School of Medical Science, Kanazawa University, Japan.
Pediatr Res. 2005 Oct;58(4):666-71. doi: 10.1203/01.PDR.0000180557.68222.5A.
To clarify the patterns of heme oxygenase-1 (HO-1) production within the human kidney, we examined HO-1 mRNA expression in various renal diseases and compared the patterns with those of HO-1 protein expression and these data with the clinical features. The degrees of hematuria and proteinuria and the levels of urinary N-acetyl-beta-D-glucosaminidase (NAG), beta(2)-microglobulin (beta(2)-mg), and creatinine were determined. In situ hybridization and immunohistochemical studies were performed to evaluate HO-1 expression. HO-1 mRNA was detectable within tubular, glomerular, and Bowman's epithelial cells and infiltrating macrophages. Within the proximal tubuli, there was a correlation between expression of HO-1 protein and mRNA, but the intensity of HO-1 mRNA expression was much less than expected from the levels of protein. In contrast, both HO-1 protein and mRNA were expressed at significant levels within distal tubuli. Furthermore, there was no correlation with both expressions within distal tubuli. HO-1 mRNA expression within tubular, glomerular, and Bowman's epithelial cells tended to be more intense with greater degrees of proteinuria. However, there was little correlation between the intensity of HO-1 mRNA expression and the degree of hematuria, NAG, and beta(2)-mg. HO-1 plays important roles in maintaining renal functions by protecting renal epithelial cells from glomerular proteinuria, which can become a cause of oxidative stress. Furthermore, from the different expression pattern of HO-1 gene between within the proximal tubuli and within the distal tubuli, renal expression of HO-1 is regulated in a segment-specific manner, with HO-1 thereby playing distinct roles in different segments of the nephron to maintain renal functions.
为阐明人肾脏中血红素加氧酶-1(HO-1)的产生模式,我们检测了各种肾脏疾病中HO-1 mRNA的表达,并将其模式与HO-1蛋白表达的模式进行比较,并将这些数据与临床特征进行比较。测定了血尿和蛋白尿的程度以及尿N-乙酰-β-D-氨基葡萄糖苷酶(NAG)、β2-微球蛋白(β2-mg)和肌酐的水平。进行原位杂交和免疫组化研究以评估HO-1的表达。在肾小管、肾小球和鲍曼上皮细胞以及浸润的巨噬细胞中可检测到HO-1 mRNA。在近端小管内,HO-1蛋白和mRNA的表达之间存在相关性,但HO-1 mRNA表达的强度远低于根据蛋白水平预期的强度。相比之下,HO-1蛋白和mRNA在远端小管内均有显著表达。此外,远端小管内两者的表达之间没有相关性。随着蛋白尿程度的增加,肾小管、肾小球和鲍曼上皮细胞内HO-1 mRNA的表达往往更强。然而,HO-1 mRNA表达的强度与血尿程度、NAG和β2-mg之间几乎没有相关性。HO-1通过保护肾上皮细胞免受肾小球蛋白尿(可成为氧化应激的原因)的影响,在维持肾功能方面发挥重要作用。此外,由于近端小管和远端小管内HO-1基因的表达模式不同,HO-1在肾脏中的表达以节段特异性方式受到调节,从而HO-1在肾单位的不同节段发挥不同作用以维持肾功能。