中华肝胆外科杂志
中華肝膽外科雜誌
중화간담외과잡지
CHINESE JOURNAL OF HEPATOBILIARY SURGERY
2009年
4期
283-287
,共5页
俞悦%张峰%李相成%姚爱华%钱晓峰%浦立勇%范烨%王学浩
俞悅%張峰%李相成%姚愛華%錢曉峰%浦立勇%範燁%王學浩
유열%장봉%리상성%요애화%전효봉%포립용%범엽%왕학호
肝移植%肝再生%肝细胞生长因子%间充质干细胞%小体积供肝
肝移植%肝再生%肝細胞生長因子%間充質榦細胞%小體積供肝
간이식%간재생%간세포생장인자%간충질간세포%소체적공간
Liver transplantation%Mesenchymal stem cell%Hepatocyte growth factor%Small-for-size graft%RegenerationDOI:10.3760/cma.j.issn.1007-8118.2009.04.015
目的 建立大鼠小体积肝移植模型,输注表达人肝细胞生长因子(human hepatocyte growth factor,hHGF)的骨髓间充质干细胞(mesenchymal stem cells,MSCs),研究其在移植早期对小移植肝促再生作用.方法 将已建立的表达hHGF和绿色荧光蛋白(green fluorescence protein,GFP)的MSCs,分别命名为HGF/MSCs,GFP/Mscs.建立大鼠30%肝移植模型.受体分为4组,实验组输注5×106HGF/MSCs;对照组则分别输注相同体积的生理盐水(PS),5×106 GFP/MSCs或1.0×109 pfu含hHGF的重组腺病毒液(Ad-HGF).分别于术后1,3,5,7 d各组随机抽取5只大鼠处死.取血检测血清ALT和hHGF.记录移植物湿重.取肝组织检测hHGF、c-met表达,以及肝细胞凋亡和增殖活性.另每组15只,分组同上,用于观察生存期.结果 PS组大鼠7 d生存率33.3%;组织学及血清学检查示术后肝脏损伤重,汇管区单核细胞浸润多;而实验组大鼠7 d生存率为73.3%.肝脏损伤轻,炎性细胞浸润少;实验组移植肝再生较PS组明显增加.结论 大鼠部分肝移植后,输注HGF/MSCs能够保护小体积移植肝,促进小移植肝再生,提高7 d生存率.
目的 建立大鼠小體積肝移植模型,輸註錶達人肝細胞生長因子(human hepatocyte growth factor,hHGF)的骨髓間充質榦細胞(mesenchymal stem cells,MSCs),研究其在移植早期對小移植肝促再生作用.方法 將已建立的錶達hHGF和綠色熒光蛋白(green fluorescence protein,GFP)的MSCs,分彆命名為HGF/MSCs,GFP/Mscs.建立大鼠30%肝移植模型.受體分為4組,實驗組輸註5×106HGF/MSCs;對照組則分彆輸註相同體積的生理鹽水(PS),5×106 GFP/MSCs或1.0×109 pfu含hHGF的重組腺病毒液(Ad-HGF).分彆于術後1,3,5,7 d各組隨機抽取5隻大鼠處死.取血檢測血清ALT和hHGF.記錄移植物濕重.取肝組織檢測hHGF、c-met錶達,以及肝細胞凋亡和增殖活性.另每組15隻,分組同上,用于觀察生存期.結果 PS組大鼠7 d生存率33.3%;組織學及血清學檢查示術後肝髒損傷重,彙管區單覈細胞浸潤多;而實驗組大鼠7 d生存率為73.3%.肝髒損傷輕,炎性細胞浸潤少;實驗組移植肝再生較PS組明顯增加.結論 大鼠部分肝移植後,輸註HGF/MSCs能夠保護小體積移植肝,促進小移植肝再生,提高7 d生存率.
목적 건립대서소체적간이식모형,수주표체인간세포생장인자(human hepatocyte growth factor,hHGF)적골수간충질간세포(mesenchymal stem cells,MSCs),연구기재이식조기대소이식간촉재생작용.방법 장이건립적표체hHGF화록색형광단백(green fluorescence protein,GFP)적MSCs,분별명명위HGF/MSCs,GFP/Mscs.건립대서30%간이식모형.수체분위4조,실험조수주5×106HGF/MSCs;대조조칙분별수주상동체적적생리염수(PS),5×106 GFP/MSCs혹1.0×109 pfu함hHGF적중조선병독액(Ad-HGF).분별우술후1,3,5,7 d각조수궤추취5지대서처사.취혈검측혈청ALT화hHGF.기록이식물습중.취간조직검측hHGF、c-met표체,이급간세포조망화증식활성.령매조15지,분조동상,용우관찰생존기.결과 PS조대서7 d생존솔33.3%;조직학급혈청학검사시술후간장손상중,회관구단핵세포침윤다;이실험조대서7 d생존솔위73.3%.간장손상경,염성세포침윤소;실험조이식간재생교PS조명현증가.결론 대서부분간이식후,수주HGF/MSCs능구보호소체적이식간,촉진소이식간재생,제고7 d생존솔.
Objective To determine whether HGF-expressing MSCs will improve small-for-size liver grafts regeneration after liver transplantation.Methods The HGF cDNA was amplified from the exprcssion plasmid pCMV-HGF by PCR and subcloned into the same site of the plasmid pDC316- IRES-EGFP vector.Virus Ad-HGF was produced by homologous recombination.BM-MSCS were cul-tured and transduced with Ad-HGF.HGF/MSCs were generated.We implanted HGF/MSCs into liv-er grafts via the portal vein using a 30% small-for-size rat liver transplantation model.HGF,c-met expression,hepatic injury and liver regeneration were assessed after liver transplantation.Results The HGF-expressing MSCs improved liver function and liver weight recovery during the early post-transplantation period,resulting in a reduced mortality in rats after small-for-size liver transplanta-tion.Conclusions The MSCs genetically modified to Over-expressing HGF and implanted in the liver graft may offer a novel approach to promoting liver regeneration after small-for-size transplantation.