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具有原代人肝细胞的三维球体和库普弗细胞在药物性肝损伤中的差异作用。

Three-Dimensional Spheroids With Primary Human Liver Cells and Differential Roles of Kupffer Cells in Drug-Induced Liver Injury.

机构信息

Corning Life Sciences, Bedford, Massachusetts 01730.

Corning Life Sciences, Bedford, Massachusetts 01730.

出版信息

J Pharm Sci. 2020 Jun;109(6):1912-1923. doi: 10.1016/j.xphs.2020.02.021. Epub 2020 Mar 5.

Abstract

Drug-induced liver injury (DILI) remains a challenge and a leading risk for drug discovery. Three-dimensional liver spheroids made from primary human hepatocytes (PHHs) with, or without, other liver cell types can provide more physiological relevance. In comparison to conventional 2-dimensional monolayer culture, our tests with 100 drugs of known DILI status indicate that PHH spheroids are significantly more sensitive in detecting drug-induced hepatotoxicity. To evaluate the role of Kupffer cells (KCs) in drug-induced liver toxicity, we have established conditions for generating co-culture spheroids with PHH and KCs. Inflammatory responses as shown by interleukin 6 secretion can be recapitulated in co-culture spheroids when treated with endotoxin lipopolysaccharides. KCs potentiated the cytotoxicity induced by trovafloxacin in co-culture spheroids at 48 h, but the differences between PHH spheroids and co-culture spheroids became less obvious after a 5-day treatment. Interestingly, a protective role of KCs was shown in co-culture spheroids treated with both acetaminophen and lipopolysaccharides. Additional tests with 14 DILI compounds comparing PHH spheroids and co-culture spheroids showed differential roles of KCs that were compound dependent. In summary, these 3-dimensional liver spheroid models are useful tools to understand the complex mechanisms underlying DILI.

摘要

药物性肝损伤(DILI)仍然是一个挑战,也是药物发现的主要风险。由原代人肝细胞(PHH)或其他肝细胞类型制成的三维肝球体可以提供更接近生理的相关性。与传统的二维单层培养相比,我们对 100 种已知具有 DILI 状态的药物的测试表明,PHH 球体在检测药物诱导的肝毒性方面明显更敏感。为了评估库普弗细胞(KCs)在药物诱导的肝毒性中的作用,我们已经建立了生成 PHH 和 KCs 共培养球体的条件。用内毒素脂多糖处理时,共培养球体中可以重现白细胞介素 6 分泌所示的炎症反应。在 48 小时时,KCs 增强了共培养球体中曲伐沙星诱导的细胞毒性,但在 5 天治疗后,PHH 球体和共培养球体之间的差异变得不那么明显。有趣的是,在同时用对乙酰氨基酚和脂多糖处理的共培养球体中,KCs 显示出保护作用。用 14 种 DILI 化合物对 PHH 球体和共培养球体进行的额外测试表明,KCs 的作用因化合物而异。总之,这些 3 维肝球体模型是了解 DILI 复杂机制的有用工具。

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