目的 研究紧密连接蛋白claudin-2在急性肾损伤(AKI)患儿肾组织中的表达变化,探讨claudin-2与肾脏病理损害及肾功能损害程度的关系。方法 2009年12月至2011年12月确诊为AKI并完善肾活检的24例患儿,依据病情严重程度分为轻症组(n=7)及重症组(n=17)。对照组为12例肾小球轻微病变的孤立性血尿患儿。采用全自动生化分析仪比色法检测血清肌酐水平;采用肾脏病理计量评分法对肾小管间质损害程度进行分析;免疫组织化学方法 检测肾组织claudin-2的表达;Pearson相关分析评估claudin-2与患儿肾脏病理评分及血肌酐水平间的关系。结果 AKI轻症组(190±68 μmol/L)与AKI重症组(477±128 μmol/L)血清肌酐水平均高于对照组(29±7 μmol/L)(均P<0.01),且AKI重症组血清肌酐水平高于AKI轻症组(P<0.01)。AKI轻症组患儿肾小管间质损害计分(10.4±1.7分)低于重症组(14.0±1.5分)(P<0.05)。AKI轻症组(5.0%±0.5%)与AKI重症组(3.7%±0.7%)claudin-2阳性表达面积均低于对照组(8.0%±0.7%)(均P<0.01),且AKI重症组claudin-2阳性表达面积低于AKI轻症组(P<0.01)。claudin-2阳性表达面积与血肌酐水平及肾小管间质的病理损害评分均呈负相关(分别r=-0.809、-0.903,均P<0.01)。结论 AKI患儿肾组织claudin-2的表达水平发生变化,且claudin-2的表达水平与肾脏病理损害程度及肾功能损害程度密切相关。
Abstract
Objective To examine changes in expression of tight junction protein claudin-2 in the renal tissues of children with acute kidney injury (AKI), and to investigate the relationship of claudin-2 expression with renal pathological lesion and renal functional lesion. Methods Twenty-four children who were diagnosed with AKI and had renal biopsies between December 2009 and December 2011 were included in the study. These patients were divided into mild AKI (n=7) and severe AKI groups (n=17). Children with isolated hematuria whose renal biopsy showed minor glomerular lesion were selected as the control group. Serum creatinine levels were measured by automatic biochemical analyzer. Tubulointerstitial damage was evaluated by renal pathological scores and expression of claudin-2 was examined by immunohistochemistry. The correlations of claudin-2 expression with renal pathological score and serum creatinine level were assessed by Pearson correlation analysis. Results The mild and severe AKI groups had significantly higher serum creatinine levels than the control group (190±68 μmol/L and 477±128 μmol/L vs 29±7 μmol/L, P<0.01), and the severe AKI group had a significantly higher serum creatinine level than the mild AKI group (P<0.01). The tubulointerstitial damage score was significantly lower in the mild AKI group than in the severe AKI group (10.4±1.7 vs 14.0±1.5; P<0.05). The mild and severe AKI groups had significantly smaller areas of claudin-2 expression than the control group (5.0±0.5% and 3.7±0.7% vs 8.0±0.7%; P<0.01), and the severe AKI group had a significantly smaller area of claudin-2 expression than the mild AKI group (P<0.01). The area of claudin-2 expression was negatively correlated with serum creatinine level and tubulointerstitial damage score (r=-0.809 and -0.903; P<0.01). Conclusions There are changes in the distribution and expression of claudin-2 in proximal tubular epithelial cells among children with AKI, and claudin-2 expression is closely related to renal pathological lesion and renal functional lesion.
关键词
急性肾损伤 /
Claudin-2 /
病理 /
肾功能 /
儿童
Key words
Acute kidney injury /
Claudin-2 /
Pathology /
Renal function /
Child
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参考文献
[1] Eadon MT, Hack BK, Xu C, et al. Endotoxemia alters tight junction gene and protein expression in the kidney[J]. Am J Physiol Renal Physiol, 2012, 303(6): F821-F830.
[2] Gonzalez JE, DiGeronimo RJ, Arthur DE, et al. Remodeling of the tight junction during recovery from exposure to hydrogen peroxide in kidney epithelial cells[J]. Free Radic Biol Med, 2009, 47(11): 1561-1569.
[3] Mehta RL, Kellum JA, Shah SV, et al. Acute Kidney Injury Network: report of an initiative to improve outcomes in acute kidney injury[J]. Crit Care, 2007, 11(2): R31.
[4] 李志辉, 易著文, 何小解, 等. 激素耐药型和激素依耐型肾病患儿肾脏病理剂量分析[J].中华儿科杂志, 2001, 39(8): 449-452.
[5] Lee DB, Huang E, Ward HJ. Tight junction biology and kidney dysfunction[J]. Am J Physiol Renal Physiol, 2006, 290(1): F20-F34.
[6] Bilder D. Epithelial polarity and proliferation control: links from the Drosophila neoplastic tumor suppressors[J]. Genes Dev, 2004, 18(16): 1909-1925.
[7] Grande M, Franzen A, Karlsson JO, et al. Transforming growth factor-beta and epidermal growth factor synergistically stimulate epithelial to mesenchymal transition (EMT) through a MEK-dependent mechanism in primary cultured pig thyrocytes[J]. J Cell Sci, 2002, 115(Pt 22): 4227-4236.
[8] Lechpammer M, Resnick MB, Sabo E, et al. The diagnostic and prognostic utility of claudin expression in renal cell neoplasms[J].Mod Pathol, 2008, 21(11): 1320-1329.
[9] Cantaluppi V, Quercia AD, Dellepiane S, et al. New mechanisms and recent insights in the pathogenesis of acute kidney injury (AKI)[J]. G Ital Nefrol, 2012, 29(5): 535-547.
[10] 陈香美, 谢院生. 急性肾损伤的修复与再生[J]. 中国中西医结合肾病杂志, 2010, 7 (11): 565-567.
[11] Reyes JL, Molina-Jijon E, Rodriguez-Munoz R, et al. Tight junction proteins and oxidative stress in heavy metals-induced nephrotoxicity[J]. Biomed Res Int, 2013, 2013: 730789.
[12] Rosenthal R, Milatz S, Krug SM, et al. Claudin-2, a component of the tight junction, forms a paracellular water channel[J]. J Cell Sci, 2010, 123(Pt 11): 1913-1921.
[13] Ikari A, Takiguchi A, Atomi K, et al. Decrease in claudin-2 expression enhances cell migration in renal epithelial Madin-Darby canine kidney cells[J]. J Cell Physiol, 2011, 226(6): 1471-1478.
[14] Arreola-Mendoza L, Del Razo LM, Mendoza-Garrido ME, et al. The protective effect of alpha-tocopherol against dichromate-induced renal tight junction damage is mediated via ERK1/2[J]. Toxicol Lett, 2009, 191(2-3): 279-288.
[15] Ikari A, Takiguchi A, Atomi K, et al. Epidermal growth factor increases clathrin-dependent endocytosis and degradation of claudin-2 protein in MDCK Ⅱ cells[J]. J Cell Physiol, 2011, 226(9): 2448-2456.
[16] Van Itallie CM, Tietgens AJ, LoGrande K, et al. Phosphorylation of claudin-2 on serine 208 promotes membrane retention and reduces trafficking to lysosomes[J]. J Cell Sci, 2012, 125(Pt 20): 4902-4912.
[17] Yasuda T, Saegusa C, Kamakura S, et al. Rab27 effector Slp2-a transports the apical signaling molecule podocalyxin to the apical surface of MDCK Ⅱ cells and regulates claudin-2 expression[J]. Mol Biol Cell, 2012, 23(16): 3229-3239.
基金
湖南省卫生厅科研基金资助项目(132013-103)。