Unraveling the Hsp70-ROS-autophagy axis in pentachlorophenol-challenged lung and liver epithelial cells

Journal Article · Mon Apr 07 00:00:00 UTC 2025 · Archives of Toxicology

DOI: https://doi.org/10.1007/s00204-025-03983-8 · OSTI ID:3014802

Thota, S. ^[1]; Begum, R. ^[1]; Mutyala, D. ^[1]; Bidarimath, N. ^[1]; Thakur, M. ^[1]; Sarkar, B. ^[2]; Morehouse, J. ^[1]; Yang, S. ^[1]; Deb, P. K. ^[2]; Dorsey, W. ^[3]; Batra, S.  ^[1]

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1. Southern University and A&M College, Baton Rouge, LA (United States)
2. Birla Institute of Technology, Jharkhand (India)
3. Grambling State University, LA (United States)

Pentachlorophenol (PCP) was extensively utilized as an organochlorine pesticide and wood preservative in the United States from the 1930s until the Environmental Protection Agency (EPA) imposed restrictions due to concerns about its toxicity and potential carcinogenic properties. Although it is no longer widely used, PCP remains a concern due to its environmental persistence and potential for long-term health effects. Significant occupational and environmental exposures have likely occurred, with the health and economic costs of PCP exposure potentially being substantial given its known toxicity. Notably, PCP exhibits rapid absorption through both the skin and respiratory system and has been shown to cause hepatotoxicity, developmental toxicity, immunotoxicity, irritation, and carcinogenicity in laboratory animal studies. PCP exposure induces oxidative stress, a key mechanism underlying its inflammatory and toxic effects, which can activate cellular stress responses including upregulation of heat shock protein 70 (Hsp70). Previous studies in lung and liver epithelial cells have shown that Hsp70 and oxidative stress play pivotal roles in triggering autophagy. This study establishes the critical role of the Hsp70-reactive oxygen species (ROS)-autophagy axis in regulating cellular responses to PCP exposure in human alveolar (A549) and liver carcinoma (HepG2) epithelial cells. Our research elucidated the molecular mechanisms underlying PCP's cellular effects, demonstrating that its exposure resulted in increased expression of autophagy-related proteins (Beclin-1, LC3B, ATG12, and ATG16), subunits of NADPH oxidase (NCF-1, NCF-2, NOX2, and Rac), and antioxidant proteins (SOD and GPx) in both lung and liver cell types. Notably, PCP augmented the interaction between Hsp70 and the autophagy regulator Beclin-1. Pretreatment with the ROS inhibitor N-acetylcysteine or Hsp70 knockdown markedly reversed PCP-induced responses. Our in-silico protein–protein docking analysis and molecular dynamics simulation studies revealed enhanced interactions and/or stable confirmations maintained throughout the simulations for TLR4-Hsp70 and Hsp70-Beclin-1 complexes in the presence of PCP. These findings provide a strong foundation for future studies, employing in vivo experimental models and human populations to identify promising targets for PCP-induced toxicity and cellular injury. As a result, these findings may have far-reaching implications for public health and environmental policy, ultimately leading to the identification of biomarkers and the development of more effective interventions for environmentally induced toxicity and diseases.

• Research Organization: Southern University and A&M College, Baton Rouge, LA (United States)
• Sponsoring Organization: DoD; National Science Foundation (NSF); USDA; USDOE National Nuclear Security Administration (NNSA)
• Grant/Contract Number: NA0004112; NA0004144
• OSTI ID: 3014802
• Report Number(s): OSTI-SUBR-4112-S26
• Journal Information: Archives of Toxicology, Journal Name: Archives of Toxicology Journal Issue: 5 Vol. 99; ISSN 0340-5761; ISSN 1432-0738
• Publisher: Springer Science and Business Media LLCCopyright Statement
• Country of Publication: United States
• Language: English