中华小儿外科杂志
中華小兒外科雜誌
중화소인외과잡지
CHINESE JOURNAL OF PEDIATRIC SURGERY
2014年
11期
853-858
,共6页
赵琦%杨屹%刘鑫%王常林%侯英%陈辉
趙琦%楊屹%劉鑫%王常林%侯英%陳輝
조기%양흘%류흠%왕상림%후영%진휘
输尿管梗阻%蛋白质组%肾盂积水%大鼠
輸尿管梗阻%蛋白質組%腎盂積水%大鼠
수뇨관경조%단백질조%신우적수%대서
Ureteral obstruction%Proteome%Hydronephrosis%Rats
目的 筛选输尿管完全梗阻(complete unilateral ureteral obstruction,CUUO)后不同时间点大鼠肾脏的差异蛋白质,并检测部分差异蛋白在输尿管梗阻大鼠肾脏及儿童先天性肾积水肾脏中的表达.方法 应用双向电泳及质谱分析技术,检测2个月龄SD大鼠CUUO后12h、24 h、72 h以及对照组四组肾脏组织差异蛋白质的表达.应用蛋白质印迹(Western blot)方法检测筛查出的差异蛋白质ANXA4和ETFB在CUUO组和正常对照组大鼠肾脏组织以及15例肾积水患儿肾脏组织及15例肾胚瘤患儿瘤旁正常肾脏组织中的表达.结果 69个表达量相差2倍以上的差异蛋白质点,经质谱分析和蛋白质数据库检索成功鉴定出39个蛋白质,涉及细胞凋亡、线粒体能量代谢及线粒体损伤、氧化应激等方面.在动物模型中ANXA4的表达随梗阻时间延长呈持续上调:CUUO12 h为0.7809±0.036,CUUO24 h为0.9385±0.013,CUUO72 h为1.0218±0.032,Sham为0.7058±0.009,组间差异有统计学意义(P<0.05);随梗阻时间的延长ETFB的表达逐渐下调:CUUO12h为0.9301±0.017,CUUO24h为0.6488±0.021,CUUO72 h为0.5452±0.018,组间差异有有统计学意义(P<0.05),而在CUUO72h组和正常对照组表达无明显差异(CUUO72 h 0.5452±0.018比Sham0.5419±0.035,P>0.05).在肾积水患儿肾脏组织中这两种蛋白的表达均显著上调(ETFB:积水组0.9322±0.014比对照组0.8325±0.012,ANXA4:积水组1.100±0.018比对照组0.8815±0.007P<0.05).结论 运用双向电泳技术结合质谱分析及生物功能信息分析筛选并鉴定出39个在CUUO大鼠肾脏中差异表达的蛋白质,这些蛋白质可能与梗阻性肾病的发生、发展有关.其中ANXA4和ETFB可能在梗阻性肾病的发生、发展过程中发挥作用.
目的 篩選輸尿管完全梗阻(complete unilateral ureteral obstruction,CUUO)後不同時間點大鼠腎髒的差異蛋白質,併檢測部分差異蛋白在輸尿管梗阻大鼠腎髒及兒童先天性腎積水腎髒中的錶達.方法 應用雙嚮電泳及質譜分析技術,檢測2箇月齡SD大鼠CUUO後12h、24 h、72 h以及對照組四組腎髒組織差異蛋白質的錶達.應用蛋白質印跡(Western blot)方法檢測篩查齣的差異蛋白質ANXA4和ETFB在CUUO組和正常對照組大鼠腎髒組織以及15例腎積水患兒腎髒組織及15例腎胚瘤患兒瘤徬正常腎髒組織中的錶達.結果 69箇錶達量相差2倍以上的差異蛋白質點,經質譜分析和蛋白質數據庫檢索成功鑒定齣39箇蛋白質,涉及細胞凋亡、線粒體能量代謝及線粒體損傷、氧化應激等方麵.在動物模型中ANXA4的錶達隨梗阻時間延長呈持續上調:CUUO12 h為0.7809±0.036,CUUO24 h為0.9385±0.013,CUUO72 h為1.0218±0.032,Sham為0.7058±0.009,組間差異有統計學意義(P<0.05);隨梗阻時間的延長ETFB的錶達逐漸下調:CUUO12h為0.9301±0.017,CUUO24h為0.6488±0.021,CUUO72 h為0.5452±0.018,組間差異有有統計學意義(P<0.05),而在CUUO72h組和正常對照組錶達無明顯差異(CUUO72 h 0.5452±0.018比Sham0.5419±0.035,P>0.05).在腎積水患兒腎髒組織中這兩種蛋白的錶達均顯著上調(ETFB:積水組0.9322±0.014比對照組0.8325±0.012,ANXA4:積水組1.100±0.018比對照組0.8815±0.007P<0.05).結論 運用雙嚮電泳技術結閤質譜分析及生物功能信息分析篩選併鑒定齣39箇在CUUO大鼠腎髒中差異錶達的蛋白質,這些蛋白質可能與梗阻性腎病的髮生、髮展有關.其中ANXA4和ETFB可能在梗阻性腎病的髮生、髮展過程中髮揮作用.
목적 사선수뇨관완전경조(complete unilateral ureteral obstruction,CUUO)후불동시간점대서신장적차이단백질,병검측부분차이단백재수뇨관경조대서신장급인동선천성신적수신장중적표체.방법 응용쌍향전영급질보분석기술,검측2개월령SD대서CUUO후12h、24 h、72 h이급대조조사조신장조직차이단백질적표체.응용단백질인적(Western blot)방법검측사사출적차이단백질ANXA4화ETFB재CUUO조화정상대조조대서신장조직이급15례신적수환인신장조직급15례신배류환인류방정상신장조직중적표체.결과 69개표체량상차2배이상적차이단백질점,경질보분석화단백질수거고검색성공감정출39개단백질,섭급세포조망、선립체능량대사급선립체손상、양화응격등방면.재동물모형중ANXA4적표체수경조시간연장정지속상조:CUUO12 h위0.7809±0.036,CUUO24 h위0.9385±0.013,CUUO72 h위1.0218±0.032,Sham위0.7058±0.009,조간차이유통계학의의(P<0.05);수경조시간적연장ETFB적표체축점하조:CUUO12h위0.9301±0.017,CUUO24h위0.6488±0.021,CUUO72 h위0.5452±0.018,조간차이유유통계학의의(P<0.05),이재CUUO72h조화정상대조조표체무명현차이(CUUO72 h 0.5452±0.018비Sham0.5419±0.035,P>0.05).재신적수환인신장조직중저량충단백적표체균현저상조(ETFB:적수조0.9322±0.014비대조조0.8325±0.012,ANXA4:적수조1.100±0.018비대조조0.8815±0.007P<0.05).결론 운용쌍향전영기술결합질보분석급생물공능신식분석사선병감정출39개재CUUO대서신장중차이표체적단백질,저사단백질가능여경조성신병적발생、발전유관.기중ANXA4화ETFB가능재경조성신병적발생、발전과정중발휘작용.
Objective To screen the differential proteins at different timepoints in rat kidney with complete unilateral ureteral obstruction (CUUO) and verify the partial differential expressions in animal model and clinical hydronephrosis.Methods Two dimensional electrophoresis (2-DE) and MALDI-TOF/TOF MS were employed to separate and identify the differential proteins in the groups of unilateral ureteral obstruction (CUUO) and corresponding sham rat kidney tissues.Western blot was used to verify the differential protein expressions of ANXA4 and ETFB in rat kidney and clinical renal tissues,including hydronephrosis (n =15) and Wilm's tumor (n =15).Results A total of 39 differential proteins whose expression levels significantly increased or decreased by over 2 folds were successfully identified by peptide mass fingerprinting.And they were involved in cell apoptosis,energy metabolism,mitochondrial injuries and oxidative stress,etc.In rat kidney,the expression of ANXA4 was continuously up-regulated with CUUO persisting (CUUO12 h:0.7809 ± 0.036,CUUO24 h:0.9385 ± 0.013,CUUO72 h:1.0218 ± 0.032,sham:0.7058 ± 0.009,P<0.05) and ETFB was continuously down-regulated with CUUO persisting (CUUO12 h:0.9301 ± 0.017,CUUO24 h:0.6488 ± 0.021,CUUO72 h:0.5452 ± 0.018,P<0.05) and the expression in CUUO72 h had no significant differences with that in control group (CUUO72 h:0.5452 ± 0.018 vs sham 0.5419 ± 0.035,P> 0.05).In clinical tissues,two proteins were both up-regulated in hydronephrosis versus control group (ETFB in hydronephrosis:0.9322 ± 0.014 vs 0.8325 ± 0.012 in control,ANXA4 in hydronephrosis:1.100 ± 0.018 vs 0.8815 ± 0.007 in control,P<0.05).Conclusions A total of 39 differentially expressed proteins probably associated with the genesis and development of obstructive nephropathy have been successfully screened from CUUO and corresponding sham kidney tissues.And ANXA4 and ETFB may be involved in the development and progression of obstructive nephropathy.