[Apoptosis induced in vitro by dexamethasone and ATP in the protoscolex of Echinococcus granulosus]

Jin-Feng Kang1, Han-Hua Hu, Wu-Mei Yuan

  • 1Xinjiang Medical University, Urumqi, China. kangjinfeng59@163.com

Abstract

Insights

Dexamethasone and adenosine triphosphate (ATP) induce apoptosis in Echinococcus granulosus protoscoleces. This study reveals potential therapeutic targets for hydatid disease by demonstrating cell shrinkage, DNA fragmentation, and increased caspase-3 activity.

Area of Science:

  • Parasitology
  • Molecular Biology
  • Cell Biology

Context:

  • Echinococcus granulosus causes hydatid disease, a significant global health concern.
  • The protoscolex is the larval stage responsible for infection establishment.
  • Understanding mechanisms of protoscolex death is crucial for developing novel treatments.

Purpose:

  • To investigate the induction of apoptosis in Echinococcus granulosus protoscoleces using dexamethasone and adenosine triphosphate (ATP).
  • To characterize the morphological and molecular changes associated with drug-induced apoptosis.

Summary:

  • Protoscoleces were cultured in vitro and treated with dexamethasone, ATP, or a combination. Morphological analysis via light and electron microscopy revealed cell shrinkage, membrane blebbing, and nuclear condensation.
  • Terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL) assay confirmed apoptotic cells. Caspase-3 activity significantly increased 12-fold, and DNA laddering was observed, indicating apoptosis induction.
  • The combination of dexamethasone and ATP showed more pronounced apoptotic effects than either agent alone.

Impact:

  • This research identifies dexamethasone and ATP as potent inducers of apoptosis in E. granulosus protoscoleces.
  • The findings provide a basis for exploring these compounds or related pathways as potential therapeutic strategies against hydatidosis.
  • Elucidating the apoptotic pathways offers new targets for anti-parasitic drug development.

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