中华肝脏病杂志
中華肝髒病雜誌
중화간장병잡지
CHINESE JOURNAL OF HEPATOLOGY
2000年
5期
274-275,278
,共3页
贾继东%王宝恩%Michael Bauer%Garbriele Boigk%Martin Rueh%Detlef Schuppan
賈繼東%王寶恩%Michael Bauer%Garbriele Boigk%Martin Rueh%Detlef Schuppan
가계동%왕보은%Michael Bauer%Garbriele Boigk%Martin Rueh%Detlef Schuppan
肝纤维化%Ⅰ型胶原%XⅧ胶原
肝纖維化%Ⅰ型膠原%XⅧ膠原
간섬유화%Ⅰ형효원%XⅧ효원
Liver fibrosis%Collagen typeⅠ%Collagen type XⅧ
目的:了解XⅧ型胶原(collagen XⅧ,CXⅧ)mRNA在实验性肝纤维化中的定量改变。 方法:以逆行胆管硬化注射加结扎的方法制备大鼠胆管堵塞性肝纤维化模型,以假手术组大鼠为对照组。提取肝脏总RNA, 以核酸酶保护分析(RNA酶保护分析)定量测定前胶原α1(XⅧ) mRNA水平,并与α1(Ⅰ) 和金属蛋白酶组织抑制因子1(TIMP-1)的mRNA变化相比较。结果:与假手术组大鼠相比,胆管堵塞性肝纤维化大鼠肝脏前胶原α1(Ⅰ)及TIMP-1 mRNA水平分别升高20倍及4倍;而肝纤维化大鼠肝脏前胶原α1(XⅧ) mRNA水平仅升高到1.8倍。结论:肝纤维化时肝脏XⅧ胶原仅轻度升高,这种变化类型可能和XⅧ胶原主要由肝实质细胞表达有关。
目的:瞭解XⅧ型膠原(collagen XⅧ,CXⅧ)mRNA在實驗性肝纖維化中的定量改變。 方法:以逆行膽管硬化註射加結扎的方法製備大鼠膽管堵塞性肝纖維化模型,以假手術組大鼠為對照組。提取肝髒總RNA, 以覈痠酶保護分析(RNA酶保護分析)定量測定前膠原α1(XⅧ) mRNA水平,併與α1(Ⅰ) 和金屬蛋白酶組織抑製因子1(TIMP-1)的mRNA變化相比較。結果:與假手術組大鼠相比,膽管堵塞性肝纖維化大鼠肝髒前膠原α1(Ⅰ)及TIMP-1 mRNA水平分彆升高20倍及4倍;而肝纖維化大鼠肝髒前膠原α1(XⅧ) mRNA水平僅升高到1.8倍。結論:肝纖維化時肝髒XⅧ膠原僅輕度升高,這種變化類型可能和XⅧ膠原主要由肝實質細胞錶達有關。
목적:료해XⅧ형효원(collagen XⅧ,CXⅧ)mRNA재실험성간섬유화중적정량개변。 방법:이역행담관경화주사가결찰적방법제비대서담관도새성간섬유화모형,이가수술조대서위대조조。제취간장총RNA, 이핵산매보호분석(RNA매보호분석)정량측정전효원α1(XⅧ) mRNA수평,병여α1(Ⅰ) 화금속단백매조직억제인자1(TIMP-1)적mRNA변화상비교。결과:여가수술조대서상비,담관도새성간섬유화대서간장전효원α1(Ⅰ)급TIMP-1 mRNA수평분별승고20배급4배;이간섬유화대서간장전효원α1(XⅧ) mRNA수평부승고도1.8배。결론:간섬유화시간장XⅧ효원부경도승고,저충변화류형가능화XⅧ효원주요유간실질세포표체유관。
Objective: To measure and study quantitatively the collagen XⅧ mRNA in normal and fibrotic rat livers. Methods: We used ribonuclease protection assay to investigate the collagen XⅧ mRNA expression in rat liver fibrosis induced by complete bile duct occlusion (BDO). The expression level of procollagen 1(XⅧ) mRNA was compared with that of procollagen 1(Ⅰ) and tissue inhibitor of metalloproteinase 1 (TIMP1). Results: mRNA levels of procollagen and TIMP 1 increased 20- and 4-fold in BDO rat livers, respectively. In contrast, hepatic procollagen 1 mRNA level increased only 1.8-fold in fibrotic rat livers. Conclusion: CXⅧ mRNA is upregulated slightly in liver fibrosis, which is probably correlated with the fact that CXⅧ is mainly expressed by hepatocytes.