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Cationic Colloidal Silica Membrane Perturbation as a Means of Examining Changes at the Sinusoidal Surface during Liver Regeneration

机译:阳离子胶体二氧化硅膜微扰作为检查肝再生过程中正弦表面变化的一种手段

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摘要

By employing the cationic colloidal silica membrane density perturbation technique, we examined growth factor receptor and extracellular matrix (ECM) changes at the sinusoidal surface during rat liver regeneration 72 hours after 70% partial hepatectomy (PHx). At this time after PHx, hepatocyte division has mostly subsided, while sinusoidal endothelial cell (SEC) proliferation is initiating, resulting in avascular hepatocyte islands. Because of the discontinuous nature of the surface of liver SEC, ECM proteins underlying the SEC, as well as SEC luminal membrane proteins, are available to absorption to the charged silica beads when the liver is perfused with the colloid. Subsequent liver homogenization and density centrifugation yield two separate fractions, enriched in SECs as well as hepatocyte basolateral membrane-specific proteins up to 50-fold over whole liver lysates. This technique facilitates examination of changes in protein composition that influence or occur as a result of SEC mitogenesis and migration during regeneration of the liver. When ECM and receptor proteins from SEC-enriched fractions were examined by Western immunoblotting, urokinase plasminogen activator receptor, fibronectin, and plasmin increased at the SEC surface 72 hours after PHx. Epidermal growth factor receptor, plasminogen, SPARC (secreted protein, acidic and rich in cysteine, also called osteonectin or BM40), and collagen IV decreased, and fibrinogen subunits and c-Met expression remained constant 72 hours after PHx when compared to control liver. These results display the usefulness of the cationic colloidal silica membrane isolation protocol. They also show considerable modulation of surface components that may regulate angiogenic processes at the end stage of liver regeneration during the reformation of sinusoids.
机译:通过使用阳离子胶体二氧化硅膜密度扰动技术,我们研究了大鼠肝脏正弦表面上生长因子受体和细胞外基质(ECM)的变化。 70%部分肝切除(PHx)后72小时再生。在PHx后的此 时间,肝细胞分裂已基本消退,而 正弦血管内皮细胞(SEC)的增殖开始,而 导致了无血管肝细胞岛。由于肝脏SEC表面的不连续 性质, SEC下的ECM蛋白以及SEC腔膜蛋白都可以用于 当肝脏向 胶体灌注时,对带电二氧化硅珠的吸收。随后的肝脏均质化和 密度离心产生两个独立的部分,在SEC中富集的 以及肝细胞基底外侧膜特异性 蛋白质多达50倍全肝裂解液。这项技术 有助于检查在肝脏再生期间 影响或由于SEC有丝分裂和迁移 而发生的蛋白质组成的变化。通过Western免疫印迹检测SEC富集馏分的ECM和受体蛋白 时,SEC上的 尿激酶纤溶酶原激活剂受体,纤连蛋白和纤溶酶 升高。 PHx后72小时的水面。表皮生长 因子受体,纤溶酶原,SPARC(分泌的蛋白,酸性 并富含半胱氨酸,也称为骨连接蛋白或BM40)和胶原蛋白 IV降低,与对照肝脏相比,PHx后72小时纤维蛋白原亚基和c-Met表达保持恒定。 这些结果表明阳离子胶体 硅胶膜分离方案。它们还显示出在正弦波再形成 的肝脏再生结束时,可能调节表面调节成分的表面成分,这些成分可能调节血管生成 的过程。

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  • 来源
    《American Journal of Pathology》 |1999年第5期|00001487-00001498|共12页
  • 作者单位

    From the Department of Cell Biology and Physiology,University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania|and the Department of Pathology,University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania;

    From the Department of Cell Biology and Physiology,University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania;

    From the Department of Cell Biology and Physiology,University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania;

    and the Department of Pathology,University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania;

    and the Department of Pathology,University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania;

    and the Department of Pathology,Akita University Medical School, Akita, Japan;

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