Affiliations 

  • 1 International Research Center for Marine Biosciences, Ministry of Science and Technology, Shanghai Ocean University, Shanghai 201306, China; Marine Biomedical Science and Technology Innovation Platform of Lin-gang Special Area, Shanghai 201306, China
  • 2 Integrative Ecophysiology, Alfred Wegener Institute, Helmholtz Centre for Polar & Marine Research, Bremerhaven, Germany
  • 3 Higher Institution Center of Excellence (HICoE), Institute of Tropical Aquaculture and Fisheries, University Malaysia Terengganu, Kuala Terengganu, Terengganu, 20000, Malaysia
  • 4 University of Geneva, Faculty of Sciences, Earth and Environment Sciences, Department F.-A. Forel for Environmental and Aquatic Sciences, CH-1211, Geneva, Switzerland
  • 5 International Research Center for Marine Biosciences, Ministry of Science and Technology, Shanghai Ocean University, Shanghai 201306, China; Marine Biomedical Science and Technology Innovation Platform of Lin-gang Special Area, Shanghai 201306, China. Electronic address: youjiwang2@gmail.com
Chemosphere, 2024 Dec 17.
PMID: 39701318 DOI: 10.1016/j.chemosphere.2024.143958

Abstract

Perfluorooctanoic acid (PFOA) functions as a surfactant, while nano-titanium dioxide (nano-TiO2) serves as an antibacterial agent. These substances are extensively utilized in industrial production and, upon release into aquatic environments, pose significant threats to the viability and development of marine organisms. However, research into the effects of PFOA and nano-TiO2 on the immune functions and cellular energy allocation (CEA) of bivalves remains limited. To investigate the impact of PFOA and nano-TiO2 on immunity and cellular energy, we exposed Mytilus coruscus individuals to different concentrations of PFOA (2 and 200 μg/L), either alone or in combination with nano-TiO2 (0.1 mg/L, particle size: 25 nm) for 14 days. We found that the co-exposure to PFOA and nano-TiO2 had significant interactive effects on multiple immune function parameters of mussels. PFOA and nano-TiO2 notably reduced the total hemocyte count (THC), esterase activity (EST), mitochondrial number (MN), lysosomal content (LYSO), and cell viability, while concurrently elevating hemocyte mortality (HM) and reactive oxygen species (ROS) levels. Some immune-related genes, such as Tumor Necrosis Factor-alpha (TNF-α) and Myeloid Differentiation Primary Response 88 (MyD88) were downregulated, while others such as Interleukin 17 (IL-17) and Transforming Growth Factor-beta (TGF-β) were upregulated after 14-day exposure to combined pollutant exposure. Furthermore, negative effects on CEA were observed under both individual and combined pollutant stress. Therefore, PFOA and nano-TiO2 regulate cellular and humoral immunity through the regulation of immune genes as mediators, while simultaneously disrupting cellular energy metabolism. The immunotoxicity of organic and particulate pollutants, and their mixtures, thus poses a significant risk to the immune defense capabilities of mussel populations in polluted coastal environments.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.