Cytotoxicity of mancozeb on Sertoli-germ cell co-culture system: Role of MAPK signaling pathway.
Mohaddeseh Mohammadi-SardooAli MandegarySeyed Noureddin Nematollahi-MahaniMahshid Moballegh NaseryMohammad NabiuniBagher AmirheidariPublished in: Toxicology and industrial health (2021)
Mancozeb (MZB) is a worldwide fungicide for the management of fungal diseases in agriculture and industrial contexts. Human exposure occurs by consuming contaminated plants, drinking water, and occupational exposure. There are reports on MZB's reprotoxicity such as testicular structure damage, sperm abnormalities, and decrease in sperm parameters (number, viability, and motility), but its molecular mechanism on apoptosis in testis remains limited. To investigate the molecular mechanisms involved in male reprotoxicity induced by MZB, we used primary cultures of mouse Sertoli-germ cells. Cells were exposed to MZB (1.5, 2.5, and 3.5 μM) for 3 h to evaluate viability by 3-[4,5-dimethylthiazol-2-yl]-2,5 diphenyl tetrazolium bromide (MTT) assay, reactive oxygen species (ROS) generation, and oxidative stress parameters (lipid peroxidation). Cell death and mitogen-activated protein kinase (MAPK) signaling were measured in these cells using flow cytometry and western blotting. In addition, some groups were exposed to N-acetylcysteine (NAC, 5 mM) in the form of co-treatment with MZB. Mancozeb reduced viability and increased the level of intracellular ROS, p38 and c-Jun N-terminal kinases (JNK) MAPK proteins phosphorylation, and apoptotic cell death, which could be blocked by NAC as an inhibitor of oxidative stress. The present study indicated for the first time the toxic manifestations of MZB on the Sertoli-germ cell co-culture. Redox imbalance and p38 and JNK signaling pathway activation might play critical roles in MZB-induced apoptosis in the male reproductive system.
Keyphrases
- induced apoptosis
- signaling pathway
- oxidative stress
- cell death
- germ cell
- cell cycle arrest
- endoplasmic reticulum stress
- pi k akt
- drinking water
- reactive oxygen species
- dna damage
- epithelial mesenchymal transition
- diabetic rats
- flow cytometry
- endothelial cells
- transcription factor
- climate change
- protein kinase
- risk assessment
- escherichia coli
- health risk
- tyrosine kinase
- cell proliferation
- induced pluripotent stem cells
- fatty acid