Cellular Distribution and Ultrastructural Changes in HaCaT Cells, Induced by Podophyllotoxin and Its Novel Fluorescent Derivative, Supported by the Molecular Docking Studies

• Published in: International journal of molecular sciences 2024-06, Vol.25 (11), p.5948
• Main Authors: Strus, Piotr, Sadowski, Karol, Kostro, Julia, Szczepankiewicz, Andrzej Antoni, Nieznańska, Hanna, Niedzielska, Magdalena, Zlobin, Andrei, Nawar Ra'idah, Pramukti, Molęda, Zuzanna, Szawkało, Joanna, Czarnocki, Zbigniew, Wójcik, Cezary, Szeleszczuk, Łukasz, Młynarczuk-Biały, Izabela
• Format: Article
• Language: English
• Subjects: Binding Sites; Cancer; Cell culture; Cell cycle; Cell death; Cell Survival - drug effects; Chemical industry; Endoplasmic Reticulum Stress - drug effects; Etoposide; Fluorescent Dyes - chemistry; HaCaT Cells; HaCaT ultrastructure; Health aspects; Herbicides; human keratinocytes; Humans; Keratinocytes - drug effects; Keratinocytes - metabolism; Ligands; Microscopy; Mitochondria - drug effects; Mitochondria - metabolism; Mitochondria - ultrastructure; Molecular Docking Simulation; Pesticides industry; Podophyllotoxin; Podophyllotoxin - analogs & derivatives; Podophyllotoxin - chemistry; Podophyllotoxin - pharmacology; podophyllotoxin docking to tubulin; podophyllotoxin with attached fluorescein; Polymerization; Toxicity; Tubulin - metabolism; Tubulins
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms25115948

Podophyllotoxin (PPT) is an active pharmaceutical ingredient (API) with established antitumor potential. However, due to its systemic toxicity, its use is restricted to topical treatment of anogenital warts. Less toxic PPT derivatives (e.g., etoposide and teniposide) are used intravenously as anticancer agents. PPT has been exploited as a scaffold of new potential therapeutic agents; however, fewer studies have been conducted on the parent molecule than on its derivatives. We have undertaken a study of ultrastructural changes induced by PPT on HaCaT keratinocytes. We have also tracked the intracellular localization of PPT using its fluorescent derivative (PPT-FL). Moreover, we performed molecular docking of both PPT and PPT-FL to compare their affinity to various binding sites of tubulin. Using the Presto blue viability assay, we established working concentrations of PPT in HaCaT cells. Subsequently, we have used selected concentrations to determine PPT effects at the ultrastructural level. Dynamics of PPT distribution by confocal microscopy was performed using PPT-FL. Molecular docking calculations were conducted using Glide. PPT induces a time-dependent cytotoxic effect on HaCaT cells. Within 24 h, we observed the elongation of cytoplasmic processes, formation of cytoplasmic vacuoles, progressive ER stress, and shortening of the mitochondrial long axis. After 48 h, we noticed disintegration of the cell membrane, progressive vacuolization, apoptotic/necrotic vesicles, and a change in the cell nucleus's appearance. PPT-FL was detected within HaCaT cells after ~10 min of incubation and remained within cells in the following measurements. Molecular docking confirmed the formation of a stable complex between tubulin and both PPT and PPT-FL. However, it was formed at different binding sites. PPT is highly toxic to normal human keratinocytes, even at low concentrations. It promptly enters the cells, probably via endocytosis. At lower concentrations, PPT causes disruptions in both ER and mitochondria, while at higher concentrations, it leads to massive vacuolization with subsequent cell death. The novel derivative of PPT, PPT-FL, forms a stable complex with tubulin, and therefore, it is a useful tracker of intracellular PPT binding and trafficking.