南方医科大学学报
南方醫科大學學報
남방의과대학학보
JOURNAL OF SOUTHERN MEDICAL UNIVERSITY
2012年
9期
1223-1229
,共7页
肝脏%线粒体蛋白组%代谢通路%发育%芯片
肝髒%線粒體蛋白組%代謝通路%髮育%芯片
간장%선립체단백조%대사통로%발육%심편
liver%mitochondrial proteome%metabolism pathways%development%microarray
目的 分析比较代谢相关蛋白在成人和胎儿肝脏中的分布及其丰度.方法 使用含19个线粒体单抗的蛋白芯片分析4种肝组织总蛋白样本(成人肝组织匀浆蛋白,胎肝匀浆蛋白,成人肝线粒体蛋白和胎肝线粒体蛋白),通过生物信息学工具对蛋白表达丰度进行比较,探讨蛋白质代谢相关的途径.结果 醛氧化酶和羰基还原酶在成人肝线粒体中的表达较胎儿分别上调2.6和1.7倍.皮质类固醇11-β3-脱氢酶同工酶1,环氧化物水解酶1和纤维蛋白原β链隘蛋白则分别下调1.7,1.9和2.2倍.环氧水解酶1和谷胱甘肽转移ω-1在成人和胎儿肝匀浆样本中存在显著差异.结论 肝脏代谢相关蛋白的表达在成人肝脏和胚胎肝脏中存在显著的差别.该研究将有助于更好地理解代谢蛋白的发生和发展,并确定肝脏代谢标志物.
目的 分析比較代謝相關蛋白在成人和胎兒肝髒中的分佈及其豐度.方法 使用含19箇線粒體單抗的蛋白芯片分析4種肝組織總蛋白樣本(成人肝組織勻漿蛋白,胎肝勻漿蛋白,成人肝線粒體蛋白和胎肝線粒體蛋白),通過生物信息學工具對蛋白錶達豐度進行比較,探討蛋白質代謝相關的途徑.結果 醛氧化酶和羰基還原酶在成人肝線粒體中的錶達較胎兒分彆上調2.6和1.7倍.皮質類固醇11-β3-脫氫酶同工酶1,環氧化物水解酶1和纖維蛋白原β鏈隘蛋白則分彆下調1.7,1.9和2.2倍.環氧水解酶1和穀胱甘肽轉移ω-1在成人和胎兒肝勻漿樣本中存在顯著差異.結論 肝髒代謝相關蛋白的錶達在成人肝髒和胚胎肝髒中存在顯著的差彆.該研究將有助于更好地理解代謝蛋白的髮生和髮展,併確定肝髒代謝標誌物.
목적 분석비교대사상관단백재성인화태인간장중적분포급기봉도.방법 사용함19개선립체단항적단백심편분석4충간조직총단백양본(성인간조직균장단백,태간균장단백,성인간선립체단백화태간선립체단백),통과생물신식학공구대단백표체봉도진행비교,탐토단백질대사상관적도경.결과 철양화매화탄기환원매재성인간선립체중적표체교태인분별상조2.6화1.7배.피질류고순11-β3-탈경매동공매1,배양화물수해매1화섬유단백원β련애단백칙분별하조1.7,1.9화2.2배.배양수해매1화곡광감태전이ω-1재성인화태인간균장양본중존재현저차이.결론 간장대사상관단백적표체재성인간장화배태간장중존재현저적차별.해연구장유조우경호지리해대사단백적발생화발전,병학정간장대사표지물.
Objective To investigate the abundance of metabolic proteins in adult and fetal human livers.Methods Adult liver homogenate proteins,fetal liver homogenate proteins,adult liver mitochondrial proteins and fetal liver mitochondrial proteins were obtained from fetal or adult liver tissues and examined using the antibody microarrays containing 19 liver monoclonal mitochondrial antibodies.The protein expression abundances were compared among the 4 protein fractions and the pathways related to protein metabolisms were explored.Results In adult liver mitochondria,aldehyde oxidase and carbonyl reductase were up-regulated by 2.6 and 1.7 folds,respectively,whereas corticosteroid 11-beta-dehydrogenase isozyme 1,epoxide hydrolase 1 and fibrinogen beta chain protein were down-regulated by 1.7,1.9 and 2.2 folds,respectively,compared to those in fetal liver mitochondria.The abundance of epoxide hydrolase 1 and glutathione transferase omega-1 was significantly different between adult and fetal liver homogenate samples.Conclusion Our results demonstrate a clear difference in the expression profiles of metabolic proteins in the liver between adults and human fetuses to allow a better understanding of the occurrence and development of the metabolic proteins and the identification of markers of liver metabolism.