Long-term exposure to environmental level of phenanthrene causes adaptive immune response and fibrosis in mouse kidneys

• Published in: Environmental pollution (1987) 2021-08, Vol.283, p.117028, Article 117028
• Main Authors: Ruan, Fengkai, Wu, Lifang, Yin, Hanying, Fang, Lu, Tang, Chen, Huang, Siyang, Fang, Longxiang, Zuo, Zhenghong, He, Chengyong, Huang, Jiyi
• Format: Article
• Language: English
• Subjects: Chronic kidney injury; ER stress; Immune disorder; Mitochondrial dysfunction; Polycyclic aromatic hydrocarbons (PAHs); T helper cell
• ISSN: 0269-7491; 1873-6424
• DOI: 10.1016/j.envpol.2021.117028

As ubiquitous, persistent organic pollutants, polycyclic aromatic hydrocarbons (PAHs) have adverse impacts on human health. Phenanthrene (Phe) is one of the most abundant PAHs in the environment. However, the long-term effects of exposure to environmental level of Phe on the kidneys and the potential mechanisms are unclear. T helper (Th) cells, a subtype of CD4+ T cells that play a central role in the renal immune microenvironment. In this study, male mice were chronically exposed to 5, 50, and 500 ng/kg bw Phe every other day for total 210 days. Those results indicated that environmental Phe exposure caused kidney hypertrophy, injury and fibrosis in the mice. Chronic, long-term environmental level of Phe exposure did not significantly alter the innate immune response but induced adaptive immune response changes (Th1/Th2 related cytokines release), causing a type 1 immune response in the 5 ng/kg bw Phe group and a type 2 immune response in the high dose groups (50 and 500 ng/kg bw). This study provides novel insights into the roles of adaptive immune response in long-term PAH exposure-induced chronic kidney injury and fibrosis, which is beneficial for further understanding the potential health hazards of PAHs and providing new avenues for immune intervention strategies to alleviate PAHs toxicity. [Display omitted] •Environmental level of Phe chronic exposure causes kidney hypertrophy and fibrosis in mice.•Adaptive immune response regulates kidney hypertrophy and fibrosis.•Mitochondrial and ER dysfunction contributes to Phe-induced kidney hypertrophy and fibrosis.