首页> 美国卫生研究院文献>Journal of the Boston Society of Medical Sciences >Cationic Colloidal Silica Membrane Perturbation as a Means of Examining Changes at the Sinusoidal Surface during Liver Regeneration
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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:通过采用阳离子胶体二氧化硅膜密度微扰技术,我们检查了70%部分肝切除(PHx)后72小时大鼠肝再生过程中正弦曲线表面生长因子受体和细胞外基质(ECM)的变化。在PHx后的此时,肝细胞分裂已基本消退,而正弦血管内皮细胞(SEC)的增殖正在启动,从而形成无血管的肝细胞岛。由于肝脏SEC表面的不连续性,当肝脏向胶体中灌注时,SEC下的ECM蛋白以及SEC腔膜蛋白可被吸收到带电的硅胶珠上。随后的肝脏均质化和密度离心产生两个独立的馏分,富含SEC和肝细胞基底外侧膜特异性蛋白,含量是整个肝溶解产物的50倍。该技术有助于检查蛋白质组成的变化,这些变化影响或发生在肝脏再生过程中的SEC有丝分裂和迁移的结果。当通过Western免疫印迹检查了富含SEC的馏分的ECM和受体蛋白时,PHx后72小时,尿激酶纤溶酶原激活剂受体,纤连蛋白和纤溶酶在SEC表面增加。与对照肝脏相比,PHx后72小时,表皮生长因子受体,纤溶酶原,SPARC(分泌的蛋白,酸性且富含半胱氨酸,也称为骨连接蛋白或BM40)和胶原蛋白IV降低,并且纤维蛋白原亚基和c-Met表达保持恒定。这些结果显示了阳离子胶体二氧化硅膜分离方案的有用性。它们还显示出表面成分的显着调节,这些表面组分可能在正弦曲线再形成期间肝脏再生的最后阶段调节血管生成过程。

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