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Godanti bhasma (anhydrous CaSO4) induces massive cytoplasmic vacuolation in mammalian cells: A model for phagocytosis assay.
Das, Subrata K; Joshi, Alpana; Bisht, Laxmi; Goswami, Vishakha; Faiz, Abul; Dutt, Gaurav; Sharma, Shiva.
Afiliação
  • Das SK; Shobhit Institute of Engineering & Technology, University, NH 58, Meerut 250110, India; Drug Discovery and Development Division, Patanjali Research Institute, Haridwar 249405, Uttarakhand, India. Electronic address: subrata.das@shobhituniversity.ac.in.
  • Joshi A; Shobhit Institute of Engineering & Technology, University, NH 58, Meerut 250110, India; Drug Discovery and Development Division, Patanjali Research Institute, Haridwar 249405, Uttarakhand, India.
  • Bisht L; Drug Discovery and Development Division, Patanjali Research Institute, Haridwar 249405, Uttarakhand, India.
  • Goswami V; Shobhit Institute of Engineering & Technology, University, NH 58, Meerut 250110, India.
  • Faiz A; Shobhit Institute of Engineering & Technology, University, NH 58, Meerut 250110, India.
  • Dutt G; Shobhit Institute of Engineering & Technology, University, NH 58, Meerut 250110, India.
  • Sharma S; Shobhit Institute of Engineering & Technology, University, NH 58, Meerut 250110, India.
Methods ; 230: 158-168, 2024 Aug 30.
Article em En | MEDLINE | ID: mdl-39216714
ABSTRACT
Phagocytosis is an essential physiological mechanism; its impairment is associated with many diseases. A highly smart particle is required for understanding detailed sequential cellular events in phagocytosis. Recently, we identified an Indian traditional medicine named Godanti Bhasma (GB), a bioactive calcium sulfate particle prepared by thermo-transformation ofgypsum. Thermal processing of the gypsum transforms its native physicochemical properties by removing water molecules into the anhydrous GB, which was confirmed by Raman and FT-IR spectroscopy. GB particle showed a 0.5-5 µm size range and a neutral surface charge. Exposure of mammalian cells to GB particles showed a rapid cellular uptake through phagocytosis and induced massive cytoplasmic vacuolation in cells. Interestingly, no cellular uptake and cytoplasmic vacuolation were observed with the parent gypsum particle. The presence of the GB particles in intra-vacuolar space was confirmed using FESEM coupled with EDX. Flow cytometry analysis and live tracking of GB-treated cells showed particle internalization, vacuole formation, particle dissolution, and later vacuolar turnover. Quantification of GB-induced vacuolation was done using neutral red uptake assay in cells. Treatment of lysosomal inhibitors (BFA1 or CQ) with GB could not induce vacuolation, suggesting the requirement of an acidic environment for the vacuolation. In the mimicking experiment, GB particle dissolution in acidic cell-free solution suggested that degradation of GB occurs by acidic pH inside the cell vacuole. Vacuole formation generally accompanies with cell death, whereas GB-induced massive vacuolation does not cause cell death. Moreover, the cell divides and proliferates with the vacuolar process, intra-vacuolar cargo degradation, and eventually vacuolar turnover. Taken together, the sequential cellular events in this study suggest that GB can be used as a smart particle for phagocytosis assay development in animal cells.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Methods Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Methods Ano de publicação: 2024 Tipo de documento: Article