中华肾脏病杂志
中華腎髒病雜誌
중화신장병잡지
2011年
7期
479-483
,共5页
钮小玲%匡新宇%张志刚%刘学光%赵仲华%张欣%徐虹%黄文彦
鈕小玲%劻新宇%張誌剛%劉學光%趙仲華%張訢%徐虹%黃文彥
뉴소령%광신우%장지강%류학광%조중화%장흔%서홍%황문언
肾小球肾炎,IgA%细胞系,转化%RGC-32%肾小管上皮细胞-间充质转分化
腎小毬腎炎,IgA%細胞繫,轉化%RGC-32%腎小管上皮細胞-間充質轉分化
신소구신염,IgA%세포계,전화%RGC-32%신소관상피세포-간충질전분화
Glomerulonephritis,IgA%Cell line,transformed%Response gene complement 32%Epithelial-mesenchymal transition
目的 研究RGC-32(response gene to complement 32)在IgA肾病(IgAN)儿童及正常肾组织中的表达及其意义.方法 用免疫组织化学方法观察IgAN儿童及正常肾组织中RGC-32蛋白的表达与分布,并与α平滑肌肌动蛋白(α-SMA)、转化生长因子β1(TGF-β1)的表达、IgAN肾组织病理损伤程度及临床相关指标进行统计学分析.结果 RGC-32蛋白在IgAN及正常肾组织的肾小管均明显表达,而在肾小球、肾小管问质及肾血管未见表达.RGC-32在正常肾组织、IgAN轻度、中度及重度损伤组中的阳性表达指数分别为(18.29±6.22)%、(23.90±9.65)%、(31.23±9.86)%和(34.52±10.63)%.RGC.32在IgAN儿童肾组织的阳性表达指数与肾小球评分、肾小管间质评分均呈正相关(r=0.385,0.347,P<0.05);与α-SMA、TGF-β1表达亦呈正相关(r=0.594,0.521,P<0.01);而与Scr、尿NAG/Cr、尿A1b/Cr、尿IgG/Cr、尿α1微球蛋白/Cr均无相关(r=0.117,-0.115,-0.138,-0.176,-0.028,P均>0.05).结论 首次发现RGC-32蛋白在IgAN儿童和正常肾组织中表达于肾小管,而在肾小球、肾小管间质及肾血管未见表达.RGC-32可能参与了IgAN患儿的肾小管间质损伤,尤其是TGF-β1诱导的肾小管上皮细胞.间充质转分化(EMT)过程.
目的 研究RGC-32(response gene to complement 32)在IgA腎病(IgAN)兒童及正常腎組織中的錶達及其意義.方法 用免疫組織化學方法觀察IgAN兒童及正常腎組織中RGC-32蛋白的錶達與分佈,併與α平滑肌肌動蛋白(α-SMA)、轉化生長因子β1(TGF-β1)的錶達、IgAN腎組織病理損傷程度及臨床相關指標進行統計學分析.結果 RGC-32蛋白在IgAN及正常腎組織的腎小管均明顯錶達,而在腎小毬、腎小管問質及腎血管未見錶達.RGC-32在正常腎組織、IgAN輕度、中度及重度損傷組中的暘性錶達指數分彆為(18.29±6.22)%、(23.90±9.65)%、(31.23±9.86)%和(34.52±10.63)%.RGC.32在IgAN兒童腎組織的暘性錶達指數與腎小毬評分、腎小管間質評分均呈正相關(r=0.385,0.347,P<0.05);與α-SMA、TGF-β1錶達亦呈正相關(r=0.594,0.521,P<0.01);而與Scr、尿NAG/Cr、尿A1b/Cr、尿IgG/Cr、尿α1微毬蛋白/Cr均無相關(r=0.117,-0.115,-0.138,-0.176,-0.028,P均>0.05).結論 首次髮現RGC-32蛋白在IgAN兒童和正常腎組織中錶達于腎小管,而在腎小毬、腎小管間質及腎血管未見錶達.RGC-32可能參與瞭IgAN患兒的腎小管間質損傷,尤其是TGF-β1誘導的腎小管上皮細胞.間充質轉分化(EMT)過程.
목적 연구RGC-32(response gene to complement 32)재IgA신병(IgAN)인동급정상신조직중적표체급기의의.방법 용면역조직화학방법관찰IgAN인동급정상신조직중RGC-32단백적표체여분포,병여α평활기기동단백(α-SMA)、전화생장인자β1(TGF-β1)적표체、IgAN신조직병리손상정도급림상상관지표진행통계학분석.결과 RGC-32단백재IgAN급정상신조직적신소관균명현표체,이재신소구、신소관문질급신혈관미견표체.RGC-32재정상신조직、IgAN경도、중도급중도손상조중적양성표체지수분별위(18.29±6.22)%、(23.90±9.65)%、(31.23±9.86)%화(34.52±10.63)%.RGC.32재IgAN인동신조직적양성표체지수여신소구평분、신소관간질평분균정정상관(r=0.385,0.347,P<0.05);여α-SMA、TGF-β1표체역정정상관(r=0.594,0.521,P<0.01);이여Scr、뇨NAG/Cr、뇨A1b/Cr、뇨IgG/Cr、뇨α1미구단백/Cr균무상관(r=0.117,-0.115,-0.138,-0.176,-0.028,P균>0.05).결론 수차발현RGC-32단백재IgAN인동화정상신조직중표체우신소관,이재신소구、신소관간질급신혈관미견표체.RGC-32가능삼여료IgAN환인적신소관간질손상,우기시TGF-β1유도적신소관상피세포.간충질전분화(EMT)과정.
Objective To examine the expression of response gene to complement 32 (RGC-32) in renal tissue of children with IgA nephropathy (IgAN), and to explore its significance. Methods The subjects were 45 children diagnosed as IgAN by renal biopsy. The expression of RGC-32, α-smooth muscle actin (α-SMA) and transforming growth factor β1 (TGF-β1) was examined by immunohistochemistry staining. The correlation of RGC-32 expression with α-SMA,TGF-β1, degree of renal pathological lesions and clinical index in IgAN was assessed by Spearman correlation analysis. Results RGC-32 protein located in renal tubular epithelial cells in normal and IgAN renal tissues. The positive expression index of RGC-32 in nomal group, IgAN mild group, moderate group and severe group was (18.29±6.22)%, (23.90±9.65)%, (31.23±9.86)%,and (34.52±10.63)% respectively. With more severity of renal pathological lesions, the expression of RGC-32 in IgAN was enhanced. The RGC-32 expression was positively correlated with the score of glomerulus and renal interstitium in children with IgAN (r=0.385, 0.347, P<0.05), as well as α-SMA, TGF-β1 (r=0.594, 0.521, P<0.01), but was not correlated with Scr, urinary NAG/Cr,Alb/Cr, IgG/Cr, and α1-M/Cr (r =0.117, -0.115, -0.138, -0.176, -0.028, all P >0.05).Conclusions RGC-32 protein locates in renal tubular epithelial cells in normal and IgAN renal tissues. RGC-32 may participate in the course of renal tubulointerstitial lesions in children with IgAN, especially in the course of epithelial-mesenchymal transition (EMT) induced by TGF-β1.