例如:"lncRNA", "apoptosis", "WRKY"

Fluoride exposure abates pro-inflammatory response and induces in vivo apoptosis rendering zebrafish (Danio rerio) susceptible to bacterial infections.

Fish Shellfish Immunol.2017 Apr;63:314-321. Epub 2017 Feb 20
Rashmi Singh 1 , Preeti Khatri 1 , Nidhi Srivastava 1 , Shruti Jain 2 , Vani Brahmachari 2 , Asish Mukhopadhyay 3 , Shibnath Mazumder 4
Rashmi Singh 1 , Preeti Khatri 1 , Nidhi Srivastava 1 , Shruti Jain 2 , Vani Brahmachari 2 , Asish Mukhopadhyay 3 , Shibnath Mazumder 4
+ et al

[No authors listed]

Author information
  • 1 Immunobiology Laboratory, Department of Zoology, University of Delhi, Delhi 110 007, India.
  • 2 Dr. B. R. Ambedkar Center for Biomedical Research, University of Delhi, Delhi 110007, India.
  • 3 National Institute of Cholera and Enteric Diseases, Kolkata, West Bengal 700010, India.
  • 4 Immunobiology Laboratory, Department of Zoology, University of Delhi, Delhi 110 007, India. Electronic address: shibnath1@yahoo.co.in.

摘要


The present study describes the immunotoxic effect of chronic fluoride exposure on adult zebrafish (Danio rerio). Zebrafish were exposed to fluoride (71.12 mg/L; 1/10 LC50) for 30 d and the expression of selected genes studied. We observed significant elevation in the detoxification pathway gene cyp1a suggesting chronic exposure to non-lethal concentration of fluoride is indeed toxic to fish. Fluoride mediated pro-oxidative stress is implicated with the downregulation in superoxide dismutase 1 and 2 (sod1/2) genes. Fluoride affected DNA repair machinery by abrogating the expression of the DNA repair gene rad51 and growth arrest and DNA damage inducible beta a gene gadd45ba. The upregulated expression of casp3a coupled with altered Bcl-2 associated X protein/B-cell lymphoma 2 ratio (baxa/bcl2a) clearly suggested chronic fluoride exposure induced the apoptotic cascade in zebrafish. Fluoride-exposed zebrafish when challenged with non-lethal dose of fish pathogen A. hydrophila revealed gross histopathology in spleen, bacterial persistence and significant mortality. We report that fluoride interferes with system-level output of pro-inflammatory cytokines tumour necrosis factor-α, interleukin-1β and interferon-γ, as a consequence, bacteria replicate efficiently causing significant fish mortality. We conclude, chronic fluoride exposure impairs the redox balance, affects DNA repair machinery with pro-apoptotic implications and suppresses pro-inflammatory cytokines expression abrogating host immunity to bacterial infections.

KEYWORDS: Apoptosis, DNA repair, Fluoride, Oxidative stress, Pro-inflammatory cytokine, Zebrafish