中华眼科杂志
中華眼科雜誌
중화안과잡지
Chinese Journal of Ophthalmology
2012年
8期
733-738
,共6页
张晓敏%焦春娜%贾喆%任新军%李筱荣%赵少贞
張曉敏%焦春娜%賈喆%任新軍%李篠榮%趙少貞
장효민%초춘나%가철%임신군%리소영%조소정
角膜移植%移植物排斥%间质干细胞
角膜移植%移植物排斥%間質榦細胞
각막이식%이식물배척%간질간세포
Corneal transplantation%Graft rejection% Mesenchymal stem cells
目的 研究尾静脉输注间充质干细胞(MSC)对大鼠角膜移植免疫排斥反应的作用.方法 实验研究.原代培养Wistar大鼠骨髓MSC,达90%融合时传代培养.制作大鼠角膜移植动物模型,以Lewis大鼠为受体,Wistar大鼠为供体,随机分为A、B、C三组.A组给予1ml不含MSC的PBS,B组术前连续3d输注MSCs,C组术后当天开始连续3d输注MSC.裂隙灯显微镜下对角膜植片进行临床观察,比较2组角膜植片的平均存活时间.A组与C组部分大鼠于术后10 d行角膜免疫组化检测角膜植片CD4、CD8、CD25和CD45的表达水平.应用Kaplan-Meier检验比较3组植片平均存活时间.免疫组化数据采用单因素方差分析及两样本均数比较的t检验.结果 C组角膜植片的存活时间为(9.9±0.69)d,与A、B组[(11.83±0.54),(16.89±1.91)d]相比均有明显延长(F=5.732;P =0.001,0.019).B组角膜植片存活时间较A组相比延长,但无统计学意义(P=0.333).C组CD4、CD8、CD25的表达水平显著低于A组(t=2.477,2.359,2.445;P=0.024,0.042,0.030).结论 术后输注MSC能显著延长大鼠同种异体角膜移植片存活时间,对大鼠角膜移植排斥反应有抑制作用.
目的 研究尾靜脈輸註間充質榦細胞(MSC)對大鼠角膜移植免疫排斥反應的作用.方法 實驗研究.原代培養Wistar大鼠骨髓MSC,達90%融閤時傳代培養.製作大鼠角膜移植動物模型,以Lewis大鼠為受體,Wistar大鼠為供體,隨機分為A、B、C三組.A組給予1ml不含MSC的PBS,B組術前連續3d輸註MSCs,C組術後噹天開始連續3d輸註MSC.裂隙燈顯微鏡下對角膜植片進行臨床觀察,比較2組角膜植片的平均存活時間.A組與C組部分大鼠于術後10 d行角膜免疫組化檢測角膜植片CD4、CD8、CD25和CD45的錶達水平.應用Kaplan-Meier檢驗比較3組植片平均存活時間.免疫組化數據採用單因素方差分析及兩樣本均數比較的t檢驗.結果 C組角膜植片的存活時間為(9.9±0.69)d,與A、B組[(11.83±0.54),(16.89±1.91)d]相比均有明顯延長(F=5.732;P =0.001,0.019).B組角膜植片存活時間較A組相比延長,但無統計學意義(P=0.333).C組CD4、CD8、CD25的錶達水平顯著低于A組(t=2.477,2.359,2.445;P=0.024,0.042,0.030).結論 術後輸註MSC能顯著延長大鼠同種異體角膜移植片存活時間,對大鼠角膜移植排斥反應有抑製作用.
목적 연구미정맥수주간충질간세포(MSC)대대서각막이식면역배척반응적작용.방법 실험연구.원대배양Wistar대서골수MSC,체90%융합시전대배양.제작대서각막이식동물모형,이Lewis대서위수체,Wistar대서위공체,수궤분위A、B、C삼조.A조급여1ml불함MSC적PBS,B조술전련속3d수주MSCs,C조술후당천개시련속3d수주MSC.렬극등현미경하대각막식편진행림상관찰,비교2조각막식편적평균존활시간.A조여C조부분대서우술후10 d행각막면역조화검측각막식편CD4、CD8、CD25화CD45적표체수평.응용Kaplan-Meier검험비교3조식편평균존활시간.면역조화수거채용단인소방차분석급량양본균수비교적t검험.결과 C조각막식편적존활시간위(9.9±0.69)d,여A、B조[(11.83±0.54),(16.89±1.91)d]상비균유명현연장(F=5.732;P =0.001,0.019).B조각막식편존활시간교A조상비연장,단무통계학의의(P=0.333).C조CD4、CD8、CD25적표체수평현저저우A조(t=2.477,2.359,2.445;P=0.024,0.042,0.030).결론 술후수주MSC능현저연장대서동충이체각막이식편존활시간,대대서각막이식배척반응유억제작용.
Objective To investigate the effect of mesenchymal stem cells (MSC) on keratoplasty rejection in a rat mode.Methods MSC from bone marrow of Wistar rats was cultured. Corneas of Wistar rats ( donors ) were transplanted to Lewis rats ( recipients ).Transplanted rats were randomly divided into A,B,C three groups.Rats in group B were injected with MSC suspended in PBS via the tail vein continually for three days before the surgery,while rats in group C accepted similar MSC transplantation after the surgery. The rats in group A were given the same volume of PBS. Grafts were scored for corneal transparency,edema and extent of neovascularization by slit lamp observation. Expressions of CD4 、CD8 、CD25 and CD45 in corneas 10 days after transplantation were examined by immunohistochemistry. Results The survival time of the corneal grafts in group C [( 9.9 ± 0.69 ) d] was significantly prnlonged compared with that of the group A and group B [(11.83 ±0.54),(16.89 ±1.91)d] (F=5.732,P=0.001,0.019). Expression level of CD4 、CD8 、CD25 of the corneal grafts in group C was lower than that of group A and group B ( t =2.477,2.359,2.445,P =0.024,0.042,0.030).Conclusion Post-operative injection of MSCs could inhibit keratoplasty rejection and prolong the corneal allografts suivival in a rat model.