Affiliation:
1. Department of Nephrology Shenzhen Key Laboratory of Kidney Diseases and Shenzhen Clinical Research Centre for Geriatrics Shenzhen People's Hospital The First Affiliated Hospital Southern University of Science and Technology Shenzhen 518020 P. R. China
2. Department of Oncology The Affiliated Hospital of Southwest Medical University 25 Taiping Street Luzhou 646000 P. R. China
3. School of Chinese Medicine Hong Kong Baptist University Kowloon Tong Hong Kong 000000 P. R. China
4. Department of Biochemistry Karpagam Academy of Higher Education Coimbatore 641021 India
5. State Key Laboratory for Quality Ensurance and Sustainable Use of Dao‐di Herbs Artemisinin Research Center and Institute of Chinese Materia Medica China Academy of Chinese Medical Sciences Beijing 100700 P. R. China
Abstract
AbstractIn recent years, there has been growing concern over the rising incidence of liver diseases, with increasing exposure to environmental toxins as a significant contributing factor. However, the mechanisms of liver injury induced by environmental pollutants are largely unclear. Here, using tetrabromobisphenol A (TBBPA), a widely used brominated flame retardant, as an example, environmental toxin‐induced liver toxicity in mice is characterized via single‐cell sequencing technology. Heterogeneous gene expression profiles after exposure to TBBPA in major cell types of the liver are demonstrated. In hepatocytes, pathway analysis of differentially expressed genes reveals the enhanced interferon response and diminished metabolic processes. The disrupted endothelial functions in TBBPA‐treated cells are then shown. Moreover, the activation of M2‐polarization in Kupffer cells, as well as activated effector T and B cells are unveiled in TBBPA‐treated cells. Finally, ligand‐receptor pair analysis shows that TBBPA disrupts cell‐cell communication and induces an inflammatory microenvironment. Overall, the results reveal that TBBPA‐induced dysfunction of hepatocytes and endothelial cells may then activate and recruit other immune cells such as Kuffer cells, and T/NK cells into the liver, further increasing inflammatory response and liver injury. Thus, the results provide novel insight into undesiring environmental pollutant‐induced liver injury.
Funder
National Key Research and Development Program of China
National Natural Science Foundation of China
Shenzhen Science and Technology Innovation Program