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用于体外评估免疫抑制物质作用的THP-1和Jurkat细胞系共培养的评估

Evaluation of THP-1 and Jurkat Cell Lines Coculture for the In Vitro Assessment of the Effects of Immunosuppressive Substances.

作者信息

Franko Nina, Sollner Dolenc Marija

机构信息

Department of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Ljubljana, SI-1000 Ljubljana, Slovenia.

出版信息

Toxics. 2024 Aug 19;12(8):607. doi: 10.3390/toxics12080607.

Abstract

The strong appeal to reduce animal testing calls for the development and validation of in vitro, in chemico and in silico models that would replace the need for in vivo testing and ex vivo materials. A category that requires such new approach methods is the assessment of immunosuppression that can be induced by chemicals including environmental pollutants. To assess the immunosuppressive action on monocytes and lymphocytes, we mimicked the whole-blood cytokine-release assay by preparing an in vitro coculture of THP-1 and Jurkat cell lines. We optimised its activation and investigated the effects of known immunosuppressive drugs with different mechanisms of action on the release of proinflammatory cytokines. Decreased secretion of IL-8 was achieved by several immunosuppressive mechanisms and was therefore selected as an appropriate marker of immunosuppression. A set of environmentally occurring bisphenols, BPA, BPAP, BPP, BPZ, BPE, TCBPA and BPS-MAE, were then applied to the model and BPP and BPZ were found to act as potent immunosuppressants at micromolar concentrations.

摘要

减少动物实验的强烈呼声促使人们开发和验证体外、化学和计算机模型,以取代体内实验和离体材料的需求。需要此类新方法的一个领域是评估包括环境污染物在内的化学物质诱导免疫抑制的情况。为了评估对单核细胞和淋巴细胞的免疫抑制作用,我们通过制备THP-1和Jurkat细胞系的体外共培养物来模拟全血细胞因子释放试验。我们优化了其激活过程,并研究了具有不同作用机制的已知免疫抑制药物对促炎细胞因子释放的影响。几种免疫抑制机制均可导致IL-8分泌减少,因此选择IL-8作为免疫抑制的合适标志物。然后将一组环境中存在的双酚,即双酚A(BPA)、双酚AP(BPAP)、双酚P(BPP)、双酚Z(BPZ)、双酚E(BPE)、四氯双酚A(TCBPA)和双酚S单烯丙基醚(BPS-MAE)应用于该模型,发现BPP和BPZ在微摩尔浓度下可作为强效免疫抑制剂发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5133/11358983/137bef1909e9/toxics-12-00607-g001.jpg

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