Related Experiment Video
Updated: Jun 27, 2026

Normothermic Cardiac Arrest and Cardiopulmonary Resuscitation: A Mouse Model of Ischemia-Reperfusion Injury
Published on: August 30, 2011
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.
Abstract:
The effect of melittin on cytosolic free Ca(2+) concentration ([Ca(2+)](i)) and viability is largely unknown. This study examined whether melittin alters Ca(2+) levels and causes Ca(2+)-dependent cell death in Madin-Darby canine kidney (MDCK) cells. [Ca(2+)](i) and cell death were measured using the fluorescent dyes fura-2 and WST-1 respectively. Melittin at concentrations above 0.5 microM increased [Ca(2+)](i) in a concentration-dependent manner. The Ca(2+) signal was reduced by 75% by removing extracellular Ca(2+). The melittin-induced Ca(2+) influx was also implicated by melittin-caused Mn(2+) influx. After pretreatment with 1 microM thapsigargin (an endoplasmic reticulum Ca(2+) pump inhibitor), melittin-induced Ca(2+) release was inhibited; and conversely, melittin pretreatment abolished thapsigargin-induced Ca(2+) release. At concentrations of 0.5-20 microM, melittin killed cells in a concentration-dependent manner. The cytotoxic effect of 0.5 microM melittin was nearly completely reversed by prechelating cytosolic Ca(2+) with BAPTA. Melittin at 0.5-2 microM caused apoptosis as assessed by flow cytometry of propidium iodide staining. Collectively, in MDCK cells, melittin induced a [Ca(2+)](i) rise by causing Ca(2+) release from endoplasmic reticulum and Ca(2+) influx from extracellular space. Furthermore, melittin can cause Ca(2+)-dependent cytotoxicity in a concentration-dependent manner.
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.
More Related Videos
15:43Assessment of Mitochondrial Functions and Cell Viability in Renal Cells Overexpressing Protein Kinase C Isozymes
Published on: January 7, 2013
07:15Mechanism of Kemeng Fang's Inhibition of Podocyte Apoptosis in Rats with Membranous Nephropathy through the PI3K/AKT Signaling Pathway
Published on: August 23, 2024
Related Concept Videos
Cellular Injury IlI: Cellular Death
Cellular Injury IV: Necrosis