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内毒素污染改变了临床前 3D 体外模型中巨噬细胞-癌细胞的相互作用和治疗效果。

Endotoxin contamination alters macrophage-cancer cell interaction and therapeutic efficacy in pre-clinical 3D in vitro models.

机构信息

Department of Advanced Organ Bioengineering and Therapeutics, Engineered Therapeutics Section, Technical Medical Centre, University of Twente, 7500AE Enschede, the Netherlands.

Rousselot bvba, Expertise Center, 9000 Gent, Belgium.

出版信息

Biomater Adv. 2023 Jan;144:213220. doi: 10.1016/j.bioadv.2022.213220. Epub 2022 Nov 26.

Abstract

The rapid developments in biofabrication, in particular 3D bioprinting, in the recent years have facilitated the need for novel biomaterials that aim to replicate the target tissue in great detail. The presence of endotoxins in these biomaterials is often an overlooked problem. In pre-clinical 3D in vitro models, endotoxins can have significant influence on cell behavior and credibility of the model. In this study we demonstrate the effects of high levels of endotoxins in commercially-available gelatin on the macrophage-cancer cell crosstalk in a 3D bioprinted co-culture model. First, it is demonstrated that, while presenting the same mechanical and structural stimuli, high levels of endotoxin can have significant influence on the metabolic activity of macrophages and cancer cells. Furthermore, this study shows that high endotoxin contamination causes a strong inflammatory reaction in macrophages and significantly inhibits the effects of a paracrine macrophage-cancer cell co-culture. At last, it is demonstrated that the differences in endotoxin levels can drastically alter the efficacy of novel macrophage modulating immunotherapies, AS1517499 and 3-methyladenine. Altogether, this study shows that endotoxin contamination in biomaterials can significantly alter intra- and intercellular communication and thereby drug efficacy, which might lead to misinterpretation of the potency and safety of the tested compounds.

摘要

近年来,生物制造领域,特别是 3D 生物打印技术的快速发展,促使人们对新型生物材料的需求日益增长,这些新型生物材料旨在高度还原目标组织。然而,这些生物材料中内毒素的存在往往被人们忽视。在内毒素存在的情况下,临床前 3D 体外模型中的细胞行为和模型的可信度都会受到显著影响。在本研究中,我们展示了商业明胶中高水平内毒素对 3D 生物打印共培养模型中巨噬细胞-癌细胞串扰的影响。首先,我们证明了虽然具有相同的机械和结构刺激,但高水平的内毒素会对巨噬细胞和癌细胞的代谢活性产生显著影响。此外,本研究表明,高水平的内毒素污染会导致巨噬细胞强烈的炎症反应,并显著抑制旁分泌巨噬细胞-癌细胞共培养的作用。最后,我们证明了内毒素水平的差异会极大地改变新型巨噬细胞调节免疫疗法(AS1517499 和 3-甲基腺嘌呤)的疗效。总的来说,本研究表明生物材料中的内毒素污染会显著改变细胞内和细胞间的通讯,从而影响药物的疗效,这可能导致对测试化合物的效力和安全性的错误解读。

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