河北医药
河北醫藥
하북의약
HEBEI MEDICAL JOURNAL
2013年
18期
2725-2727,2728
,共4页
许秀芳%辛毅%张颖%黄益民%顾云%林筝%孟旭%周玉杰%张兆光
許秀芳%辛毅%張穎%黃益民%顧雲%林箏%孟旭%週玉傑%張兆光
허수방%신의%장영%황익민%고운%림쟁%맹욱%주옥걸%장조광
大鼠心脏移植模型%外周血淋巴细胞多基因差异表达时相%淋巴细胞表面蛋白分子CD4%CD8分子表达时相
大鼠心髒移植模型%外週血淋巴細胞多基因差異錶達時相%淋巴細胞錶麵蛋白分子CD4%CD8分子錶達時相
대서심장이식모형%외주혈림파세포다기인차이표체시상%림파세포표면단백분자CD4%CD8분자표체시상
heart transplantation model,rats%peripheral blood lymphocyte%multi-gene differential expression phase%lymphocyte surface protein molecule%CD4,CD8 molecule expression phase
目的建立大鼠异体异位心脏移植动物模型,观察心脏移植前后淋巴细胞多基因表达和CD4、CD8分子表达及环孢素A对其影响。方法 SD大鼠为供体,Wistar大鼠为受体,分为心脏移植对照组和环孢素A干预两组。移植前、移植后24 h、3 d、7 d、10 d和12 d测定外周血淋巴细胞CD4、CD8分子表达、荧光差异显示分析淋巴细胞编码基因表达水平。结果(1)移植组:7个基因差异表达,比同组的CD4和CD8分子开始正调表达的时间提前24 h;(2)环孢素A组外周血淋巴细胞的基因表达水平发生变化的有5个基因差异表达;(3)环孢素A组2.3-bisphosphoglycerate 比对照组的第一个正调表达时相至少晚24 h,环孢素A还可抑制心脏移植后7 d内外周血淋巴细胞对gig18基因的转录;移植后24 h内,环孢素A组外周血淋巴细胞Na-通道蛋白基因正调表达。结论淋巴细胞多基因差异表达及与表面蛋白分子表达时相比较对于深入研究移植排斥反应机制和环孢素A的作用机制具有一定的意义。
目的建立大鼠異體異位心髒移植動物模型,觀察心髒移植前後淋巴細胞多基因錶達和CD4、CD8分子錶達及環孢素A對其影響。方法 SD大鼠為供體,Wistar大鼠為受體,分為心髒移植對照組和環孢素A榦預兩組。移植前、移植後24 h、3 d、7 d、10 d和12 d測定外週血淋巴細胞CD4、CD8分子錶達、熒光差異顯示分析淋巴細胞編碼基因錶達水平。結果(1)移植組:7箇基因差異錶達,比同組的CD4和CD8分子開始正調錶達的時間提前24 h;(2)環孢素A組外週血淋巴細胞的基因錶達水平髮生變化的有5箇基因差異錶達;(3)環孢素A組2.3-bisphosphoglycerate 比對照組的第一箇正調錶達時相至少晚24 h,環孢素A還可抑製心髒移植後7 d內外週血淋巴細胞對gig18基因的轉錄;移植後24 h內,環孢素A組外週血淋巴細胞Na-通道蛋白基因正調錶達。結論淋巴細胞多基因差異錶達及與錶麵蛋白分子錶達時相比較對于深入研究移植排斥反應機製和環孢素A的作用機製具有一定的意義。
목적건립대서이체이위심장이식동물모형,관찰심장이식전후림파세포다기인표체화CD4、CD8분자표체급배포소A대기영향。방법 SD대서위공체,Wistar대서위수체,분위심장이식대조조화배포소A간예량조。이식전、이식후24 h、3 d、7 d、10 d화12 d측정외주혈림파세포CD4、CD8분자표체、형광차이현시분석림파세포편마기인표체수평。결과(1)이식조:7개기인차이표체,비동조적CD4화CD8분자개시정조표체적시간제전24 h;(2)배포소A조외주혈림파세포적기인표체수평발생변화적유5개기인차이표체;(3)배포소A조2.3-bisphosphoglycerate 비대조조적제일개정조표체시상지소만24 h,배포소A환가억제심장이식후7 d내외주혈림파세포대gig18기인적전록;이식후24 h내,배포소A조외주혈림파세포Na-통도단백기인정조표체。결론림파세포다기인차이표체급여표면단백분자표체시상비교대우심입연구이식배척반응궤제화배포소A적작용궤제구유일정적의의。
Objective To establish the animal models of variant heterotopic cardiac transplantation in rats in order to observe the effects of lymphocyte multi-gene expression and CD4,CD8 molecule expression as well as cyclosporin A before and after heart transplantation .Methods SD rats were used as donor and Wistar rats were used as recipient .The rats were divided into two groups, transplantation control group and cyclosporine A intervention group.The CD 4, CD8 molecule expression levels in peripheral blood lymphocyte were detected respectively at 24h, 72h,7d,10d, 12d before and after heart transplantation ,and the expression levels of lymphocyte coding gene were analyzed by fluorescence differential display .Results ( 1 ) Tansplantation control group: there were 7 genes differential expression , which were 24h earlier than CD4, CD8 molecular positive regulation expression.(2) Cyclosporine A intervention group:there were 5 genes differential expression in peripheral blood lymphocyte.(3) Cyclosporine A intervention group: 2.3-bisphosphoglycerate positive regulation expression was 24h later than that of control group,fuethermore,cyclosporine A could also inhibit gig18 gene transcription of peripheral blood lymphocyte within 7d after heart transplantation.Within 24h after heart transplantation,sodium channel protein gene was expressed positively in peripheral blood lymphocyte of cyclosporine A intervention group . Conclusion The comparison between lymphocyte multi-gene differential expression and lymphocyte surface protein molecule expression phase plays an important role in researching deeply the transplant rejection reaction mechanism and the action mechanism of cyclosporine A .