中国组织工程研究
中國組織工程研究
중국조직공정연구
Journal of Clinical Rehabilitative Tissue Engineering Research
2012年
53期
9960-9964
,共5页
靳小石%矫政洧%张爱民%程树杰%刘彤%王鹏志
靳小石%矯政洧%張愛民%程樹傑%劉彤%王鵬誌
근소석%교정유%장애민%정수걸%류동%왕붕지
环孢素%转化生长因子 β1%小肠移植%排斥反应%器官移植
環孢素%轉化生長因子 β1%小腸移植%排斥反應%器官移植
배포소%전화생장인자 β1%소장이식%배척반응%기관이식
背景:小肠移植慢性排斥反应的发生是影响其长远预后的重要因素.目的:观察环孢素对于小肠移植物中转化生长因子β1表达的影响.方法:近交系 F344(RT11vr)大鼠和 Lewis(RT11)大鼠作为小肠移植的供体和受体,利用显微外科技术构建异系大鼠小肠移植模型,分别在建模后7,28,60 d 进行移植物活检,常规病理学检测,应用 Real time-PCR 技术检测移植物内转化生长因子β1因子 mRNA 转录水平,并采用免疫组织化学方法对转化生长因子β1的表达进行定位.结果与结论:在建模后7-28 d 应用环孢素的过程中转化生长因子β1 mRNA 转录水平呈现明显减低趋势;在28-60 d,停用环孢素后该因子表达则明显升高.说明环孢素对于异系小肠移植中转化生长因子β1的表达有一定的抑制作用.
揹景:小腸移植慢性排斥反應的髮生是影響其長遠預後的重要因素.目的:觀察環孢素對于小腸移植物中轉化生長因子β1錶達的影響.方法:近交繫 F344(RT11vr)大鼠和 Lewis(RT11)大鼠作為小腸移植的供體和受體,利用顯微外科技術構建異繫大鼠小腸移植模型,分彆在建模後7,28,60 d 進行移植物活檢,常規病理學檢測,應用 Real time-PCR 技術檢測移植物內轉化生長因子β1因子 mRNA 轉錄水平,併採用免疫組織化學方法對轉化生長因子β1的錶達進行定位.結果與結論:在建模後7-28 d 應用環孢素的過程中轉化生長因子β1 mRNA 轉錄水平呈現明顯減低趨勢;在28-60 d,停用環孢素後該因子錶達則明顯升高.說明環孢素對于異繫小腸移植中轉化生長因子β1的錶達有一定的抑製作用.
배경:소장이식만성배척반응적발생시영향기장원예후적중요인소.목적:관찰배포소대우소장이식물중전화생장인자β1표체적영향.방법:근교계 F344(RT11vr)대서화 Lewis(RT11)대서작위소장이식적공체화수체,이용현미외과기술구건이계대서소장이식모형,분별재건모후7,28,60 d 진행이식물활검,상규병이학검측,응용 Real time-PCR 기술검측이식물내전화생장인자β1인자 mRNA 전록수평,병채용면역조직화학방법대전화생장인자β1적표체진행정위.결과여결론:재건모후7-28 d 응용배포소적과정중전화생장인자β1 mRNA 전록수평정현명현감저추세;재28-60 d,정용배포소후해인자표체칙명현승고.설명배포소대우이계소장이식중전화생장인자β1적표체유일정적억제작용.
BACKGROUND: The chronic rejection of intestinal graft is the important factor affecting the long term prognosis. OBJECTIVE: To observe the effect of cyclosporine A on the expression of transforming growth factor-β1 in intestinal graft in rats. METHODS: Al ogeneic smal intestine transplantation was performed in rats by microsurgical technology with the donor of F344(RT11vr) rats and the recipient of Lewis(RT11) rats. The graft biopsy and routine pathologic examination were performed at 7, 28 and 60 days after modeling. mRNA transcription level of transforming growth factor-β1 was detected by real time-PCR. Immunohistochemical staining was also performed to detect the expression of transforming growth factor-β1. RESULTS AND CONCLUSION: The mRNA transcription level of transforming growth factor-β1 was significantly decreased during the application of cyclosporine A at 7-28 days after modeling. At 28-60 days after modeling, the mRNA transcription level was significantly increased after termination of cyclosporine A. Cyclosporine A can inhibit the expression of transforming growth factor-β1 in al ogeneic smal intestine transplantation.