Mercury Chloride but Not Lead Acetate Causes Apoptotic Cell Death in Human Lung Fibroblast MRC5 Cells via Regulation of Cell Cycle Progression.
Ji-Young KimMi-Jin AnGeun-Seup ShinHyun-Min LeeMi Jin KimChul-Hong KimJung-Woong KimPublished in: International journal of molecular sciences (2021)
Heavy metals are important for various biological systems, but, in excess, they pose a serious risk to human health. Heavy metals are commonly used in consumer and industrial products. Despite the increasing evidence on the adverse effects of heavy metals, the detailed mechanisms underlying their action on lung cancer progression are still poorly understood. In the present study, we investigated whether heavy metals (mercury chloride and lead acetate) affect cell viability, cell cycle, and apoptotic cell death in human lung fibroblast MRC5 cells. The results showed that mercury chloride arrested the sub-G1 and G2/M phases by inducing cyclin B1 expression. In addition, the exposure to mercury chloride increased apoptosis through the activation of caspase-3. However, lead had no cytotoxic effects on human lung fibroblast MRC5 cells at low concentration. These findings demonstrated that mercury chloride affects the cytotoxicity of MRC5 cells by increasing cell cycle progression and apoptotic cell death.
Keyphrases
- cell death
- cell cycle arrest
- cell cycle
- heavy metals
- induced apoptosis
- risk assessment
- cell proliferation
- human health
- pi k akt
- endoplasmic reticulum stress
- health risk assessment
- health risk
- healthcare
- oxidative stress
- emergency department
- signaling pathway
- climate change
- wastewater treatment
- wound healing
- drinking water
- health information