The dynamin inhibitor, dynasore, prevents zoledronate-induced viability loss in human gingival fibroblasts by partially blocking zoledronate uptake and inhibiting endosomal acidification

Authors

  • Jacob Kirby Indiana Wesleyan University. Division of Natural Sciences
  • Makayla Standfest Indiana Wesleyan University. Division of Natural Sciences https://orcid.org/0000-0003-3333-4958
  • Jessica Binkley Indiana Wesleyan University, Division of Natural Sciences
  • Charles Barnes Indiana Wesleyan University. Division of Natural Sciences
  • Evan Brown Indiana Wesleyan University. Division of Natural Sciences
  • Tyler Cairncross Indiana Wesleyan University. Division of Natural Sciences
  • Alex Cartwright Indiana Wesleyan University. Division of Natural Sciences
  • Danielle Dadisman Indiana Wesleyan University. Division of Natural Sciences
  • Colten Mowat Indiana Wesleyan University. Division of Natural Sciences
  • Daniel Wilmot Indiana Wesleyan University. Division of Natural Sciences https://orcid.org/0009-0007-8443-391X
  • Theodore Houseman Indiana Wesleyan University. Division of Natural Sciences
  • Conner Murphy Indiana Wesleyan University. Division of Natural Sciences
  • Caleb Engelsman Indiana Wesleyan University. Division of Natural Sciences
  • Josh Haller Indiana Wesleyan University. Division of Natural Sciences
  • Daniel Jones Indiana Wesleyan University. Division of Natural Sciences https://orcid.org/0000-0001-7162-1558

DOI:

https://doi.org/10.1590/1678-7757-2024-0224

Keywords:

Bisphosphonate-associated osteonecrosis of the jaw, Dynamins, Endosomes, Fibroblasts, Zoledronic acid

Abstract

Objective: For treatment of medication-related osteonecrosis of the jaw, one proposed approach is the use of a topical agent to block entry of these medications in oral soft tissues. We tested the ability of phosphonoformic acid (PFA), an inhibitor of bisphosphonate entry through certain sodium-dependent phosphate contransporters (SLC20A1, 20A2, 34A1-3) as well as Dynasore, a macropinocytosis inhibitor, for their abilities to prevent zoledronate-induced (ZOL) death in human gingival fibroblasts (HGFs). Methodology: MTT assay dose-response curves were performed to determine non-cytotoxic levels of both PFA and Dynasore. In the presence of 50 μM ZOL, optimized PFA and Dynasore doses were tested for their ability to restore HGF viability. To determine SLC expression in HGFs, total HGF RNA was subjected to quantitative real-time RT-PCR. Confocal fluorescence microscopy was employed to see if Dynasore inhibited macropinocytotic HGF entry of AF647-ZOL. Endosomal acidification in the presence of Dynasore was measured by live cell imaging utilizing LysoSensor Green DND-189. As a further test of Dynasore’s ability to interfere with ZOL-containing endosomal maturation, perinuclear localization of mature endosomes containing AF647-ZOL or TRITC-dextran as a control were assessed via confocal fluorescence microscopy with CellProfiler™ software analysis of the resulting photomicrographs. Results: 0.5 mM PFA did not rescue  HGFs from ZOL-induced viability loss at 72 hours while 10 and 30 μM geranylgeraniol did partially rescue. HGFs did not express the SLC transporters as compared to the expression in positive control tissues. 10 μM Dynasore completely prevented ZOL-induced viability loss. In the presence of Dynasore, AF647-ZOL and FITC-dextran co-localized in endosomes. Endosomal acidification was inhibited by Dynasore and perinuclear localization of both TRITC-dextran- and AF647-ZOL-containing endosomes was inhibited by 30 μM Dynasore. Conclusion: Dynasore prevents ZOL-induced viability loss in HGFs by partially interfering with macropinocytosis and by inhibiting the endosomal maturation pathway thought to be needed for ZOL delivery to the cytoplasm.

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Published

2024-09-30 — Updated on 2024-10-01

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How to Cite

Kirby, J., Standfest, M., Binkley, J., Barnes, C., Brown, E., Cairncross, T., Cartwright, A., Dadisman, D., Mowat, C., Wilmot, D., Houseman, T., Murphy, C., Engelsman, C., Haller, J., & Jones, D. (2024). The dynamin inhibitor, dynasore, prevents zoledronate-induced viability loss in human gingival fibroblasts by partially blocking zoledronate uptake and inhibiting endosomal acidification. Journal of Applied Oral Science, 32, e20240224. https://doi.org/10.1590/1678-7757-2024-0224 (Original work published 2024)