Related Experiment Video
Updated: Jul 28, 2026

10:46
Mechanical Stimulation-induced Calcium Wave Propagation in Cell Monolayers: The Example of Bovine Corneal Endothelial Cells
Published on: July 16, 2013
A membrane model for cytosolic calcium oscillations. A study using Xenopus oocytes
1Department of Neurology, Mount Sinai School of Medicine, New York, New York 10029.
Biophysical Journal
|July 1, 1992
Summary
Mathematical models reveal how cellular calcium oscillations are generated. The study shows that calcium flux and buffering levels control oscillation frequency and amplitude, offering insights into cellular signaling.
Area of Science:
- Cell Biology
- Biophysics
- Computational Biology
Background:
- Cytosolic calcium oscillations are crucial for diverse cellular functions.
- Understanding the mechanisms driving these oscillations is essential for cell signaling research.
Purpose of the Study:
- To develop a mathematical model of cytosolic calcium oscillations.
- To investigate the role of the endoplasmic reticulum (ER) membrane properties in generating these oscillations.
- To determine factors influencing the frequency and amplitude of calcium oscillations.
Main Methods:
- A mathematical model was created based on the electrophysiological properties of the ER membrane.
- The model incorporated calcium-dependent channels and pumps, constant calcium entry, calcium removal, and protein buffering.
- Numerical integration was used to simulate cytosolic calcium concentration, ER membrane potential, and calcium binding protein dynamics.
Main Results:
- The model successfully reproduced key physiological features required for calcium oscillations.
- Calcium flux into the cytosol was identified as a primary determinant of oscillation frequency and amplitude.
- Buffering capacity of cytoplasmic proteins was shown to significantly affect oscillation characteristics.
Conclusions:
- The developed mathematical model provides a framework for understanding cytosolic calcium oscillations.
- ER membrane properties, calcium flux, and buffering are critical for regulating calcium signaling dynamics.
- The findings have implications for studying cellular responses and dysfunctions involving calcium signaling.

