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胶原蛋白凝胶通过激活核因子κB(NF-κB)保护L929细胞免受肿瘤坏死因子α(TNFα)诱导的死亡。

Collagen gel protects L929 cells from TNFα-induced death by activating NF-κB.

作者信息

Wang Hong-Ju, Li Meng-Qi, Liu Wei-Wei, Hayashi Toshihiko, Fujisaki Hitomi, Hattori Shunji, Tashiro Shin-Ichi, Onodera Satoshi, Ikejima Takashi

机构信息

a China-Japan Research Institute of Medical and Pharmaceutical Sciences , Shenyang Pharmaceutical University , Shenyang , China.

b Nippi Research Institute of Biomatrix, Nippi, Incorporated , Toride , Japan.

出版信息

Connect Tissue Res. 2017 Sep;58(5):456-463. doi: 10.1080/03008207.2016.1248287. Epub 2016 Oct 20.

Abstract

PURPOSE

Type I collagen is one of the most abundant components of extracellular matrix. We previously illustrated that murine fibrosarcoma L929 cells grew well on type I collagen gel and escaped from TNFα-induced cell death. In this study, we investigated the mechanism underlying the protective effect of collagen gel.

MATERIAL AND METHODS

We used western blot, confocal microscopy, MTT assay and flow cytometry by introducing fluorescence staining to determine the expression levels of nuclear factor kappa B (NF-κB), inhibitory ratio and autophagy.

RESULTS

L929 cells on collagen gel showed higher expression of NF-κB in the nucleus. Inhibition of NF-κB with pyrrolidine dithiocarbamate hydrochloride (PDTC) or knockdown by NF-κB-siRNA canceled the protective effect of collagen gel on L929 cells from TNFα-induced death, suggesting for the role of NF-κB in the protection from cell death. We found a new aspect of the effect of PDTC on L929 cells cultured on collagen gel. PDTC alone without TNFα induced apoptosis in the L929 cells cultured on collagen gel but not the cells on plastic dish. The apoptosis induction of the L929 cells cultured on collagen gel with PDTC was repressed by inhibiting autophagy with chloroquine, an autophagy inhibitor, suggesting that autophagy contributes to the death induced by the treatment with PDTC. Possible underlying mechanism of this finding is discussed.

CONCLUSION

NF-κB played an important role in protecting the L929 cells cultured on collagen gel from TNFα-induced death.

摘要

目的

I型胶原蛋白是细胞外基质中最丰富的成分之一。我们之前曾表明,小鼠纤维肉瘤L929细胞在I型胶原蛋白凝胶上生长良好,并能逃避肿瘤坏死因子α(TNFα)诱导的细胞死亡。在本研究中,我们探究了胶原蛋白凝胶保护作用的潜在机制。

材料与方法

我们通过引入荧光染色,采用蛋白质免疫印迹法、共聚焦显微镜技术、MTT法和流式细胞术来测定核因子κB(NF-κB)的表达水平、抑制率和自噬情况。

结果

胶原蛋白凝胶上的L929细胞在细胞核中显示出较高的NF-κB表达。用盐酸吡咯烷二硫代氨基甲酸盐(PDTC)抑制NF-κB或通过NF-κB小干扰RNA(NF-κB-siRNA)敲低NF-κB,均可消除胶原蛋白凝胶对L929细胞免受TNFα诱导死亡的保护作用,这表明NF-κB在保护细胞免于死亡中发挥作用。我们发现了PDTC对在胶原蛋白凝胶上培养的L929细胞作用的一个新方面。单独使用PDTC而无TNFα时,可诱导在胶原蛋白凝胶上培养的L929细胞凋亡,但对塑料培养皿上的细胞无此作用。用自噬抑制剂氯喹抑制自噬可抑制PDTC诱导的在胶原蛋白凝胶上培养的L929细胞凋亡,这表明自噬促成了PDTC处理诱导的细胞死亡。本文讨论了这一发现可能的潜在机制。

结论

NF-κB在保护在胶原蛋白凝胶上培养的L929细胞免受TNFα诱导的死亡中发挥重要作用。

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