解剖学报
解剖學報
해부학보
ACTA ANATOMICA SINICA
2010年
2期
262-266
,共5页
张艳萍%刘凯%尹海燕%贾颐舫%吴爱华
張豔萍%劉凱%尹海燕%賈頤舫%吳愛華
장염평%류개%윤해연%가이방%오애화
维甲酸%神经管畸形%Dishevelled2%Vangl2%原位杂交%免疫组织化学%小鼠
維甲痠%神經管畸形%Dishevelled2%Vangl2%原位雜交%免疫組織化學%小鼠
유갑산%신경관기형%Dishevelled2%Vangl2%원위잡교%면역조직화학%소서
Retinoic acid%Neural tube defect%Dishevelled2%Vangl2%In situ hybridization%Immunohistochemistry%Mouse
目的 探讨Dishevelled2和Vangl 2蛋白与过量维甲酸致昆明小鼠神经管畸形发生的关系.方法 50只昆明孕小鼠随机分为对照组和实验组.孕7.75d时,实验组一次性胃饲30mg/kg致畸量维甲酸(RA),对照组胃饲等量溶剂,服药后4h、18h、42h、66h及90h分别取胚胎,常规石蜡切片,采用原位杂交和免疫组织化学技术,分别检测胚胎神经管组织中Dishevelled2蛋白和Vangl2 mRNA及蛋白的表达水平变化. 结果 两种蛋白均存在于对照组及实验组不同发育阶段的小鼠神经管上皮,且两者的表达变化趋势有所不同.与对照组相比,实验组Dishevelled2蛋白在RA处理18h、42h时表达水平明显降低(P≤0.05),66h时表达升高(P≤0.05),90h时两组表达水平无明显差异;Vangl2 mRNA在灌服RA 4h、18h时表达水平明显低于对照组(P≤0.05),42h时两组表达水平无明显差异,66h时表达显著高于对照组(P≤0.05).Vangl2蛋白在RA处理18h、42h时表达显著降低(P≤0.05),66h时两组表达水平无明显差异,90h时表达显著高于对照组(P≤0.05). 结论 过量RA可能通过调节Dishevelled2和Vangl2表达干扰正常胚胎神经管的闭合过程.
目的 探討Dishevelled2和Vangl 2蛋白與過量維甲痠緻昆明小鼠神經管畸形髮生的關繫.方法 50隻昆明孕小鼠隨機分為對照組和實驗組.孕7.75d時,實驗組一次性胃飼30mg/kg緻畸量維甲痠(RA),對照組胃飼等量溶劑,服藥後4h、18h、42h、66h及90h分彆取胚胎,常規石蠟切片,採用原位雜交和免疫組織化學技術,分彆檢測胚胎神經管組織中Dishevelled2蛋白和Vangl2 mRNA及蛋白的錶達水平變化. 結果 兩種蛋白均存在于對照組及實驗組不同髮育階段的小鼠神經管上皮,且兩者的錶達變化趨勢有所不同.與對照組相比,實驗組Dishevelled2蛋白在RA處理18h、42h時錶達水平明顯降低(P≤0.05),66h時錶達升高(P≤0.05),90h時兩組錶達水平無明顯差異;Vangl2 mRNA在灌服RA 4h、18h時錶達水平明顯低于對照組(P≤0.05),42h時兩組錶達水平無明顯差異,66h時錶達顯著高于對照組(P≤0.05).Vangl2蛋白在RA處理18h、42h時錶達顯著降低(P≤0.05),66h時兩組錶達水平無明顯差異,90h時錶達顯著高于對照組(P≤0.05). 結論 過量RA可能通過調節Dishevelled2和Vangl2錶達榦擾正常胚胎神經管的閉閤過程.
목적 탐토Dishevelled2화Vangl 2단백여과량유갑산치곤명소서신경관기형발생적관계.방법 50지곤명잉소서수궤분위대조조화실험조.잉7.75d시,실험조일차성위사30mg/kg치기량유갑산(RA),대조조위사등량용제,복약후4h、18h、42h、66h급90h분별취배태,상규석사절편,채용원위잡교화면역조직화학기술,분별검측배태신경관조직중Dishevelled2단백화Vangl2 mRNA급단백적표체수평변화. 결과 량충단백균존재우대조조급실험조불동발육계단적소서신경관상피,차량자적표체변화추세유소불동.여대조조상비,실험조Dishevelled2단백재RA처리18h、42h시표체수평명현강저(P≤0.05),66h시표체승고(P≤0.05),90h시량조표체수평무명현차이;Vangl2 mRNA재관복RA 4h、18h시표체수평명현저우대조조(P≤0.05),42h시량조표체수평무명현차이,66h시표체현저고우대조조(P≤0.05).Vangl2단백재RA처리18h、42h시표체현저강저(P≤0.05),66h시량조표체수평무명현차이,90h시표체현저고우대조조(P≤0.05). 결론 과량RA가능통과조절Dishevelled2화Vangl2표체간우정상배태신경관적폐합과정.
Objective To explore the relationship between the expression of Dishevelled2 and Vangl2 and the embryonic neural tube defects (NTDs) induced by all-trans retinoic acid (RA)in Kunming mouse. Methods Fifty pregnant mice were randomly divided into control and RA-treated groups.RA-treated mice were fed with 30mg/kg RA dissolved with peanut oil on embryo 7.75 days, while the mice of control group were administrated with an equal volume of peanut oil on the same time. Then all the embryos were sampled from pregnant mice at the 4th, 18th, 42nd, 66th and 90th hour after treatment. In situ hybridization and immunohistochemical staining technique were used to detect the expression of Dishevelled2 and Vangl2 in embryonic neural tube. Results The two proteins both existed in the epithelial tissue of the mouse embryonic neural tube and displayed different expression modes at various developmental stages.Compared with the control group, the RA treated group showed a significant decrease (P≤0.05) at the 18th and 42nd hour and a significant increase (P≤0.05) at the 66th hour in Dishevelled2 protein after maternal treatment, and no significant difference was found at the 90th hour. Compared with the control group, the Vangl2 mRNA expression in the RA treated group displayed a significant decrease (P≤0.05) at the 4th and 18th hour and a significant increase (P≤0.05) at the 66th hour after RA treatment, and no difference was found at the 42nd hour. Compared with the control group, the expression of Vangl2 protein in the RA treated group decreased (P≤0.05) at the 18th and 42nd hour, and increased (P≤0.05) at the 90th hour after RA treatment, no difference was found at the 66th hour. Conclusion Excessive RA may interfere with the normal embryonic neural tube closure by regulating the expression of Dishevelled2 and Vangl2.
