中国组织工程研究
中國組織工程研究
중국조직공정연구
Journal of Clinical Rehabilitative Tissue Engineering Research
2014年
28期
4555-4562
,共8页
曹燕雯%魏亚明%李瑜元%聂玉强%吴倩
曹燕雯%魏亞明%李瑜元%聶玉彊%吳倩
조연문%위아명%리유원%섭옥강%오천
干细胞%移植%炎症性肠病%间充质干细胞%表达谱基因芯片%国家自然科学基金
榦細胞%移植%炎癥性腸病%間充質榦細胞%錶達譜基因芯片%國傢自然科學基金
간세포%이식%염증성장병%간충질간세포%표체보기인심편%국가자연과학기금
mesenchymal stem celltransplantation%Crohn disease%intestine,large%gene expression profiling%microchip analytical procedures
背景:前期研究已证明间充质干细胞可定植于炎症性肠黏膜修复炎症性肠组织。目的:应用表达谱芯片技术研究间充质干细胞移植修复前后大鼠炎症性大肠组织的差异基因表达情况,初步揭示与间充质干细胞定植、分化、修复炎症性肠组织过程相关的主导基因。方法:健康SD大鼠随机分为2组:移植实验组用三硝基苯磺酸灌肠制作炎症性肠病模型,造模后24 h经尾静脉注入绿色荧光蛋白标记的间充质干细胞;对照组以生理盐水代替三硝基苯磺酸同法灌肠处理。于移植后28 d取移植实验组和对照组大肠组织,利用基因芯片技术筛选移植实验组和对照组的差异表达基因。结果与结论:对照组和移植实验组大肠组织全基因组表达谱芯片结果有差异性表达的基因共388个(P<0.05, FC>2),其中表达上调基因191个、表达下调基因197个,主要与炎症反应、免疫反应和细胞分化3个方面有关。前10位显著上调和下调的差异基因(共20条)中,与炎症反应相关的有3个,与免疫反应相关的有3个,与干细胞分化相关的有2个。388个差异基因主要涉及33条信号通路(P <0.05),其中与炎症反应相关的有6条,与免疫反应相关的有8条,与干细胞分化相关的有5条。结果可见利用全基因组表达谱基因芯片的方法初步筛选了间充质干细胞修复炎症性肠组织的主要相关基因。
揹景:前期研究已證明間充質榦細胞可定植于炎癥性腸黏膜脩複炎癥性腸組織。目的:應用錶達譜芯片技術研究間充質榦細胞移植脩複前後大鼠炎癥性大腸組織的差異基因錶達情況,初步揭示與間充質榦細胞定植、分化、脩複炎癥性腸組織過程相關的主導基因。方法:健康SD大鼠隨機分為2組:移植實驗組用三硝基苯磺痠灌腸製作炎癥性腸病模型,造模後24 h經尾靜脈註入綠色熒光蛋白標記的間充質榦細胞;對照組以生理鹽水代替三硝基苯磺痠同法灌腸處理。于移植後28 d取移植實驗組和對照組大腸組織,利用基因芯片技術篩選移植實驗組和對照組的差異錶達基因。結果與結論:對照組和移植實驗組大腸組織全基因組錶達譜芯片結果有差異性錶達的基因共388箇(P<0.05, FC>2),其中錶達上調基因191箇、錶達下調基因197箇,主要與炎癥反應、免疫反應和細胞分化3箇方麵有關。前10位顯著上調和下調的差異基因(共20條)中,與炎癥反應相關的有3箇,與免疫反應相關的有3箇,與榦細胞分化相關的有2箇。388箇差異基因主要涉及33條信號通路(P <0.05),其中與炎癥反應相關的有6條,與免疫反應相關的有8條,與榦細胞分化相關的有5條。結果可見利用全基因組錶達譜基因芯片的方法初步篩選瞭間充質榦細胞脩複炎癥性腸組織的主要相關基因。
배경:전기연구이증명간충질간세포가정식우염증성장점막수복염증성장조직。목적:응용표체보심편기술연구간충질간세포이식수복전후대서염증성대장조직적차이기인표체정황,초보게시여간충질간세포정식、분화、수복염증성장조직과정상관적주도기인。방법:건강SD대서수궤분위2조:이식실험조용삼초기분광산관장제작염증성장병모형,조모후24 h경미정맥주입록색형광단백표기적간충질간세포;대조조이생리염수대체삼초기분광산동법관장처리。우이식후28 d취이식실험조화대조조대장조직,이용기인심편기술사선이식실험조화대조조적차이표체기인。결과여결론:대조조화이식실험조대장조직전기인조표체보심편결과유차이성표체적기인공388개(P<0.05, FC>2),기중표체상조기인191개、표체하조기인197개,주요여염증반응、면역반응화세포분화3개방면유관。전10위현저상조화하조적차이기인(공20조)중,여염증반응상관적유3개,여면역반응상관적유3개,여간세포분화상관적유2개。388개차이기인주요섭급33조신호통로(P <0.05),기중여염증반응상관적유6조,여면역반응상관적유8조,여간세포분화상관적유5조。결과가견이용전기인조표체보기인심편적방법초보사선료간충질간세포수복염증성장조직적주요상관기인。
BACKGROUND:Previous studies have verified that mesenchymal stem cells could be transplanted into inflammatory bowel mucosa to repair inflammatory bowel tissue. OBJECTIVE:To observe the differential gene expression in large intestine before and after mesenchymal stem celltransplantation in repair of inflammatory bowel tissue of rats using microarray technology, and to primarily discover the main genes during mesenchymal stem celltransplantation, differentiation, and reparation in inflammatory colorectal tissue region. METHODS:Healthy Sprague-Dawley rats were randomly divided into two groups. Experimental rat models of inflammatory bowel disease were established using trinitrobenzene sulfonic acid via enema. At 24 hours after model establishment, green fluorescent protein-labeled mesenchymal stem cells were infused via the caudal vein. The control group was treated with physiological saline by enema, instead of trinitrobenzene sulfonic acid. At 28 days, large intestine was obtained from the experimental group and control group. Differential y expressed genes were screened in the experimental and control groups using microarray technique. RESULTS AND CONCLUSION:The microarray analysis results showed that there were 388 differential genes in the control and experimental groups (P<0.05, FC>2), in which 191 were up-expressed, and 197 were down-expressed. Al of these genes were mainly involved in inflammatory reaction, immune reaction and celldifferentiation. In the top 10 up-regulation and down-regulation differential genes (total y 20 genes), 3 genes were involved in inflammation, 3 genes were involved in immune reaction, and 2 genes were related to stem celldifferentiation. In the 388 genes, 33 were related to signaling pathways (P<0.05), 6 related to inflammation, 8 related to immunity, and 5 related to stem celldifferentiation. Results suggested that the main genes involved in mesenchymal stem cells in repair of inflammatory bowel tissue were primarily screened using gene expression microarray technique.