Melittin-induced [Ca2+]i increases and subsequent death in canine renal tubular cells

S I Liu1, H H Cheng, C J Huang

  • 1Department of Surgery, Kaohsiung Veterans General Hospital, Kaohsiung, Taiwan.

Insights

Melittin increases intracellular calcium levels by affecting endoplasmic reticulum release and extracellular influx in kidney cells. This calcium increase leads to melittin-induced, calcium-dependent cell death and apoptosis.

Area of Science:

  • Cell Biology
  • Toxicology
  • Biochemistry

Background:

  • The impact of melittin on intracellular calcium ([Ca2+]i) and cell viability remains poorly understood.
  • Melittin, a peptide toxin, is known to interact with cell membranes.

Purpose of the Study:

  • To investigate how melittin affects cytosolic free Ca(2+) concentration ([Ca2+]i) in Madin-Darby canine kidney (MDCK) cells.
  • To determine if melittin-induced cell death is dependent on altered Ca(2+) levels.

Main Methods:

  • Measurements of [Ca2+]i using fura-2 fluorescence.
  • Assessment of cell viability using WST-1 assay.
  • Analysis of apoptosis via propidium iodide staining and flow cytometry.

Main Results:

  • Melittin elevated [Ca2+]i in a concentration-dependent manner above 0.5 microM, primarily through extracellular Ca(2+) influx and endoplasmic reticulum release.
  • Melittin induced significant cell death at concentrations of 0.5-20 microM, which was reversed by chelating intracellular Ca(2+).
  • Melittin treatment (0.5-2 microM) triggered apoptosis in MDCK cells.

Conclusions:

  • Melittin disrupts Ca(2+) homeostasis in MDCK cells by promoting both Ca(2+) influx and release from intracellular stores.
  • Melittin-induced cytotoxicity is mediated by elevated intracellular Ca(2+) levels, leading to cell death and apoptosis.