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实验性肝纤维化肝内Ⅰ、Ⅲ型胶原及PⅢP的免疫组化研究 被引量:2

THE IMMUNOHISTOUCHEMISTRY OF COLLAGEN TYPEⅠ,ⅢAND PⅢ P IN CCL_4-INDUCED FIBROTIC LIVER IN RAT
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摘要 利用免疫组化ABC法研究正常及CCl4实验性肝纤维化大鼠肝内,Ⅰ、Ⅲ型胶原及PⅢP的分布,并对部分切片进行了图像定量分析。结果表明在正常肝脏,Ⅰ、Ⅲ型胶原在分布上一致,PⅢP在汇管区显著少于Ⅰ、Ⅲ型胶原(P<0.001),在肝窦周围显著多于Ⅰ、Ⅲ型胶原(P<0.01,P<0.05),提示汇管区以成熟胶原为主,在肝窦周围以新合成胶原为主。在肝纤维化时,胶原纤维分布于变性、坏死的肝细胞之间,呈“干枝挂果”样,肝窦周围的胶原随着纤维化的进展而减少。纤维隔来源于非实质细胞,肝细胞可能不参与胶原合成。 Using the immunohistochemical ABC technique, the distribution of collagen type Ⅰ, Ⅲ and P ⅢP in normal and CCl4 -induced fibrotic liver were investigated in rat. Some of the patho- logical sections were analyzed by imaging analysis system, and the collagen distribution in sinusoid and portal triads was quantified. The results revealed that the collagen type Ⅰ and Ⅲ had the same distribution pattern. In normal rat liver, the quantity of PⅢP was significantly less than:that of collagen type Ⅰ and Ⅲ in portal triads(P<0. 01) and more abundant in sinusoid(P<0. 01 , P< 0. 05 respectively). We deduced that in sinusoid,,he leading component was newly synthesized col- lagen , while the mature collagen. accounted for the majority in portal triads. In fibrotic rat liver, the collagen was distributed among the degenerated and necrotic hepatocytes, while the portal colla- gen radiated into the parenchyma, The sinusoidal collagen was gradually decreased as fibrosis pro- gressing; the mechanism of this phenomenon was unknown, The fibrotic septa was originated from the nonparenchymal cells , and the hepdtocytes might not be involved in the synthesis of collagen.
出处 《解放军医学杂志》 CAS CSCD 北大核心 1994年第1期12-15,共4页 Medical Journal of Chinese People's Liberation Army
关键词 肝硬变 胶原 免疫组织化学 Liver cirrhosis Experimental study of collagen Immunohistochemistry
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