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游离和微囊化肝细胞培养物中肝刺激物质的释放:初步报告

Release of hepatic stimulatory substance from cultures of free and microencapsulated hepatocytes: preliminary report.

作者信息

Kashani S A, Chang T M

机构信息

Artificial Cells and Organs Research Centre, Faculty of Medicine, McGill University, Montreal, P.Q., Canada.

出版信息

Biomater Artif Cells Artif Organs. 1988;16(4):741-6. doi: 10.3109/10731198809117566.

Abstract

The galactosamine induced liver failure animal model was used to study the release of hepatic stimulatory substance (HSS) from free and microencapsulated hepatocytes in culture. Free hepatocyte cultures released HSS which significantly increased DNA synthesis in hepatocyte and the survival time of this animal model. The release HSS was not observed when hepatocytes were microencapsulated in an alginate matrix. The alginate matrix has a pore size which does not allow molecules larger than albumin (64,000 M.W.) to pass through the matrix. This suggests that of the two different ranges of molecular weights suggested for the hepatic stimulatory substance, those in the higher molecular range are important for liver regeneration.

摘要

利用半乳糖胺诱导的肝衰竭动物模型,研究游离和微囊化肝细胞在培养过程中肝刺激物质(HSS)的释放情况。游离肝细胞培养物释放出的HSS可显著增加肝细胞中的DNA合成以及该动物模型的存活时间。当肝细胞被微囊化在藻酸盐基质中时,未观察到HSS的释放。藻酸盐基质的孔径不允许大于白蛋白(分子量64,000)的分子通过该基质。这表明,对于所提出的肝刺激物质的两个不同分子量范围,较高分子量范围内的那些物质对肝脏再生很重要。

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