医学临床研究
醫學臨床研究
의학림상연구
JOURNAL OF CLINICAL RESEARCH
2015年
5期
898-901
,共4页
杨鹏%杨雷%李庆志%马宪友%祝沪军%张临友
楊鵬%楊雷%李慶誌%馬憲友%祝滬軍%張臨友
양붕%양뢰%리경지%마헌우%축호군%장림우
肺移植%再灌注损伤%细胞 ,培养的%肺泡/细胞学%上皮细胞
肺移植%再灌註損傷%細胞 ,培養的%肺泡/細胞學%上皮細胞
폐이식%재관주손상%세포 ,배양적%폐포/세포학%상피세포
Lung Transplantation%Reperfusion Injury%Cells,Cultured%Pulmonary Alveoli/CY%Epithelial Cells
【目的】在体外模拟临床肺移植,建立起肺移植缺血再灌注损伤(ischemia reperfusion injury ,IRI)的细胞模型。【方法】将人肺泡上皮细胞系A549用Perfadex液保存于100%氧气,4℃环境中来模拟缺血过程,缺血时间分为6h、12h、18h、24h,然后加入37℃含10%胎牛血清的DM EM培养基来模拟再灌注过程,再灌注时间为2 h。分别检测超氧化物歧化酶(SOD)、丙二醛(MDA)、乳酸脱氢酶(LDH)含量,并应用CCK‐8测细胞存活率。【结果】与对照组相比,各时间点试验组M DA、LD H含量逐渐增加,而SOD含量和细胞存活率则逐渐降低。各时间点MDA、LDH、SOD、细胞存活率水平也存在差异。【结论】成功建立了肺移植IRI细胞模型,此模型能够在分子与细胞水平研究肺移植IRI机制。
【目的】在體外模擬臨床肺移植,建立起肺移植缺血再灌註損傷(ischemia reperfusion injury ,IRI)的細胞模型。【方法】將人肺泡上皮細胞繫A549用Perfadex液保存于100%氧氣,4℃環境中來模擬缺血過程,缺血時間分為6h、12h、18h、24h,然後加入37℃含10%胎牛血清的DM EM培養基來模擬再灌註過程,再灌註時間為2 h。分彆檢測超氧化物歧化酶(SOD)、丙二醛(MDA)、乳痠脫氫酶(LDH)含量,併應用CCK‐8測細胞存活率。【結果】與對照組相比,各時間點試驗組M DA、LD H含量逐漸增加,而SOD含量和細胞存活率則逐漸降低。各時間點MDA、LDH、SOD、細胞存活率水平也存在差異。【結論】成功建立瞭肺移植IRI細胞模型,此模型能夠在分子與細胞水平研究肺移植IRI機製。
【목적】재체외모의림상폐이식,건립기폐이식결혈재관주손상(ischemia reperfusion injury ,IRI)적세포모형。【방법】장인폐포상피세포계A549용Perfadex액보존우100%양기,4℃배경중래모의결혈과정,결혈시간분위6h、12h、18h、24h,연후가입37℃함10%태우혈청적DM EM배양기래모의재관주과정,재관주시간위2 h。분별검측초양화물기화매(SOD)、병이철(MDA)、유산탈경매(LDH)함량,병응용CCK‐8측세포존활솔。【결과】여대조조상비,각시간점시험조M DA、LD H함량축점증가,이SOD함량화세포존활솔칙축점강저。각시간점MDA、LDH、SOD、세포존활솔수평야존재차이。【결론】성공건립료폐이식IRI세포모형,차모형능구재분자여세포수평연구폐이식IRI궤제。
[Objective]To establish a novel cell model imitating clinical lung transplantation that can be applied in the study of Ischemia reperfusion injury (IRI) in lung transplantation .[Methods] A549 cells ,a human pulmonary epithelial cell line ,were preserved in 100% O2 at 4℃ for 6 ,12 ,18 ,and 24h in Perfadex solution ,simulating ische‐mia .Then introduce 37℃ DMEM plus 10% fetal bovine serum to simulate reperfusion for a period of 2 h .The con‐tent of malondialdehyde(MDA) ,superoxide dismutase(SOD) and lactate dehydrogenase(LDH) were measured ,The cell survival rate of A549 was determined by CCK‐8 assay .[Results]The content of MDA、LDH of each experimental group gradually decreased and the content of SOD and the cell survival rate gradually increased than control group . There was difference in the content of MDA ,LDH ,SOD and the cell survival rate in each experimental group .[Con‐clusions] The lung transplantation IRI cell model was successfully established .This model could be used to study mechanisms related to IRI at the cellular and molecular level .