An experimental model of acute liver injury using multicellular spheroids composed of rat parenchymal and non-parenchymal liver cells.

K Endoh, K Ueno, A Miyashita, T Satoh
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Abstract

Massive hepatic cell necrosis can be induced by Corynebacterium parvum and lipopolysaccharide (LPS) in rats. In this model, serum LDH, GOT and GPT activities are significantly increased in vivo within several hours after LPS injection. An in vitro experimental acute liver injury animal model was produced by using multicellular spheroids composed of rat parenchymal and non-parenchymal liver cells. These multicellular spheroids were prepared by detaching the confluent monolayer on the collagen-conjugated thermo-responsive polymer coated culture dish at a temperature below the lower critical solution temperature and culturing it on the non-adhesive substratum. LPS caused clear elevations of GOT, GPT and LDH activities from these spheroids into the medium. However, the increase of LDH activity was only observed in the monolayer culture system. These results suggest that the multicellular spheroids of liver cells are useful models as an alternative to animal tests for hepatotoxicity.

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用大鼠实质和非实质肝细胞组成的多细胞球体建立急性肝损伤的实验模型。
小棒状杆菌和脂多糖可诱导大鼠肝细胞大量坏死。LPS注射后数小时内,大鼠体内血清LDH、GOT和GPT活性显著升高。采用大鼠实质肝细胞和非实质肝细胞组成的多细胞球体制备体外实验性急性肝损伤动物模型。这些多细胞球体是在低于最低临界溶液温度的温度下,将胶原偶联热响应聚合物包被培养皿上的融合单层分离,并在不粘附的基质上培养而成的。LPS使这些球体进入培养基的GOT、GPT和LDH活性明显升高。然而,LDH活性的增加只在单层培养体系中观察到。这些结果表明,肝细胞的多细胞球体是一种有用的模型,可以替代动物肝毒性试验。
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