共 73 条
Combined effect of polystyrene microplastics and bisphenol A on the human embryonic stem cells-derived liver organoids: The hepatotoxicity and lipid accumulation
被引:31
作者:
Cheng, Wei
[1
,5
]
Zhou, Yue
[1
]
Xie, Yichun
[1
]
Li, Yan
[1
]
Zhou, Ren
[2
]
Wang, Hui
[3
]
Feng, Yan
[1
]
Wang, Yan
[4
,6
]
机构:
[1] Shanghai Jiao Tong Univ, Sch Publ Hlth, Sch Med, Shanghai, Peoples R China
[2] Shanghai Jiao Tong Univ, Ninth Peoples Hosp, Sch Med, Shanghai, Peoples R China
[3] Shanghai Jiao Tong Univ, Ctr Single Cell Omics, Sch Publ Hlth, State Key Lab Oncogenes & Related Genes,Sch Med, Shanghai, Peoples R China
[4] Shanghai Jiao Tong Univ, Ninth Peoples Hosp, Shanghai Collaborat Innovat Ctr Translat Med,Sch M, Sch Publ Hlth, Shanghai, Peoples R China
[5] 280 South Chongqing Rd, Shanghai 200025, Peoples R China
[6] Bld 8,639 Zhizaoju Rd, Shanghai 200011, Peoples R China
关键词:
Human embryonic stem cells;
Liver organoids;
Combined effect;
BPA;
Microplastics;
Non -static exposure;
IN-VITRO;
CHEMICALS;
TOXICITY;
BINDING;
BPA;
D O I:
10.1016/j.scitotenv.2022.158585
中图分类号:
X [环境科学、安全科学];
学科分类号:
08 ;
0830 ;
摘要:
Human are exposed to microplastics (MP) via inhalation or ingestion daily and inevitably. The liver is an important target organ of MP. Bisphenol A (BPA) is one of commonly used plasticizers. It is added in plastics, but also generally detected in the biological samples of human beings. However, the combined toxic effect of MP and BPA on human liver is unclear. In this study, a novel 3D in vitro model, the liver organoid (LO) derived from human-pluripotent stem cells, has been utilized to explore the 1 mu m polystyrene (PS)-induced hepatotoxicity with BPA individually and jointly. Conclusively, all the changes in the cytotoxicity, cellular and molecular makers regarding the energy supplement, hepatic injury, oxidative stress, inflammatory response, disruption in the lipid accumulation, as well as epigenetics regulation induced by BPA or PS on the LOs individually were comparable to previous study. The BPA levels in the culture medium were declined by the added PS. The combined adverse effect of PS and BPA on the LOs was identified to be synergistic upon deteriorated hepatotoxicity and interfered the gene panels related to multiple processes of lipid metabolism, together with the proteins of HNF4A, CD36, ACC1, CPT1A, CYP2E1, ER alpha and ER beta. Specifically, PS didn't change the ER alpha or ER beta individually, but when the LOs were co-exposed to PS and BPA, the ER alpha further elevated significantly and synergistically. Our findings highlight the metabolic-related health risk due to co-exposure to MP and BPA, even at low-doses equivalent to human internal exposure level. Based on these findings, the potential adverseoutcome pathway related to PS and BPA singly and jointly were proposed, predicting two possible outcomes to be hepatic steatosis. Moreover, the ER alpha and HNF4A were proposed to be potential candidate markers to investigate the "vector-like effect" of PS in the present of BPA.
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页数:17
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