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在HEK293-TLR4报告细胞系模型中,常见的食品添加剂卡拉胶不是Toll样受体4(TLR4)的配体。

The common food additive carrageenan is not a ligand for Toll-Like- Receptor 4 (TLR4) in an HEK293-TLR4 reporter cell-line model.

作者信息

McKim James M, Wilga Paul C, Pregenzer Jeffrey F, Blakemore William R

机构信息

IONTOX, LLC, 4717 Campus Dr., Kalamazoo, MI 49008, USA.

Cyprotex/CeeTox, Inc., 4717 Campus Dr., Kalamazoo, MI 49008, USA.

出版信息

Food Chem Toxicol. 2015 Apr;78:153-8. doi: 10.1016/j.fct.2015.01.003. Epub 2015 Jan 29.

Abstract

Carrageenan (CGN) is widely used in the food manufacturing industry as an additive that stabilizes and thickens food products. Standard animal safety studies in which CGN was administered in diet showed no adverse effects. However, several in vitro studies have reported that intestinal inflammation is caused by CGN and that this effect is mediated through Toll-Like-Receptor 4 (TLR4). The purpose of this study was to evaluate the ability of different types of CGN to bind and activate TLR4 signaling. To accomplish this a TLR4/MD-2/CD14/NFκB/SEAP reporter construct in a HEK293 cell line was used. The reporter molecule, secretable alkaline phosphatase (SEAP), was measured as an indicator of TLR4 activation. The test compounds were exposed to this system at concentrations of 0.1, 1, 10, 50, 100, 500, 1000, and 5000 ng/mL for 24 h. Cytotoxicity was evaluated following the 24 h exposure period by LDH leakage and ATP. CGN binding to serum proteins was characterized by Toluidine Blue. The results show that CGN does not bind to TLR4 and is not cytotoxic to the HEK293 cells at the concentrations and experimental conditions tested and that CGN binds tightly to serum proteins.

摘要

角叉菜胶(CGN)作为一种能使食品稳定和增稠的添加剂,在食品制造业中被广泛使用。在标准动物安全性研究中,给动物喂食CGN未显示出不良影响。然而,多项体外研究报告称,CGN会引发肠道炎症,且这种作用是通过Toll样受体4(TLR4)介导的。本研究的目的是评估不同类型的CGN结合并激活TLR4信号传导的能力。为实现这一目的,在人胚肾293(HEK293)细胞系中使用了一种TLR4/MD-2/CD14/NFκB/SEAP报告基因构建体。作为TLR4激活指标,对报告分子分泌型碱性磷酸酶(SEAP)进行了检测。将测试化合物以0.1、1、10、50、100、500、1000和5000 ng/mL的浓度暴露于该系统24小时。在24小时暴露期后,通过乳酸脱氢酶(LDH)泄漏和三磷酸腺苷(ATP)评估细胞毒性。用甲苯胺蓝表征CGN与血清蛋白的结合情况。结果表明,在测试的浓度和实验条件下,CGN不与TLR4结合,对HEK293细胞无细胞毒性,且CGN与血清蛋白紧密结合。

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