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比较人肺上皮细胞暴露于 PM 时的配体组学分析。

Comparative Ligandomic Analysis of Human Lung Epithelial Cells Exposed to PM .

机构信息

School of Public Health, Xinxiang Medical University, Xinxiang 453003, Henan, China.

Bascom Palmer Eye Institute, Department of Ophthalmology, University of Miami School of Medicine, Miami 33136, Florida, USA.

出版信息

Biomed Environ Sci. 2020 Mar 20;33(3):165-173. doi: 10.3967/bes2020.023.

Abstract

OBJECTIVE

To investigate whether exposure to particulate matter of diameter equal to or less than 2.5 μm (PM ) alters the response of lung epithelial cells to extrinsic regulation by globally profiling cell surface ligands and quantifying their binding activity.

METHODS

Human A549 lung epithelial cells (LECs) were treated with or without PM . Ligandomic profiling was applied to these cells for the global identification of LEC-binding ligands with simultaneous quantification of binding activity. Quantitative comparisons of the entire ligandome profiles systematically identified ligands with increased or decreased binding to PM -treated LECs.

RESULTS

We found 143 ligands with increased binding to PM -treated LECs and 404 ligands with decreased binding. Many other ligands showed no change in binding activity. For example, apolipoprotein E (ApoE), Notch2, and growth arrest-specific 6 (Gas6) represent ligands with increased, decreased, or unchanged binding activity, respectively. Both ApoE and Gas6 are phagocytosis ligands, suggesting that phagocytic receptors on LECs after stimulation with PM were differentially upregulated by PM .

CONCLUSION

These results suggest that the newly-developed ligandomics is a valuable approach to globally profile the response of LECs to PM in terms of regulating the expression of cell surface receptors, as quantified by ligand binding activity. This quantitative ligandome profiling will provide in-depth understanding of the LEC molecular response on the cell surface to particulate matter air pollution.

摘要

目的

通过对细胞表面配体进行全谱分析并量化其结合活性,研究直径等于或小于 2.5μm 的颗粒物(PM )暴露是否改变肺上皮细胞对外在调节的反应。

方法

用或不用 PM 处理人 A549 肺上皮细胞(LEC)。对这些细胞进行配体组学分析,以全面鉴定与 LEC 结合的配体,并同时量化其结合活性。对整个配体组谱进行定量比较,系统地鉴定出与 PM 处理的 LEC 结合增加或减少的配体。

结果

我们发现 143 种配体与 PM 处理的 LEC 结合增加,404 种配体与 PM 处理的 LEC 结合减少。许多其他配体的结合活性没有变化。例如,载脂蛋白 E(ApoE)、Notch2 和生长停滞特异性 6(Gas6)分别代表结合活性增加、减少或不变的配体。ApoE 和 Gas6 都是吞噬作用的配体,表明 PM 刺激后 LEC 上的吞噬受体被 PM 差异地上调。

结论

这些结果表明,新开发的配体组学是一种有价值的方法,可以从定量配体结合活性的角度全面分析 LEC 对 PM 的反应,从而调节细胞表面受体的表达。这种定量配体组谱分析将深入了解 LEC 对颗粒物空气污染的细胞表面分子反应。

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