[Calcium-permeable cation channel activated by growth factors]
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Updated: Aug 19, 2026

Single-Cell Calcium Imaging for Studying the Activation of Calcium Ion Channels
Published on: December 13, 2024
1Institute for Molecular and Cellular Regulation, Gunma University.
Abstract:
Calcium is required for cell-cycle progression. Growth factors which promote G(1) progression activate calcium-permeable cation channels and induce sustained increase in calcium entry. Inhibition of these channels blocks the action of growth factors. Despite of the physiological significance, little is known about the molecular nature of the growth factor-regulated channels. Recently, primary structure of GRC-1, one of growth factor-regulated channel, was identified.
Insights
Growth factors regulate cell cycle progression by activating calcium channels. The identification of GRC-1, a key growth factor-regulated channel, advances understanding of calcium
Area of Science:
- Cell Biology
- Molecular Biology
- Physiology
Context:
- Calcium ions (Ca2+) are essential for cell cycle progression.
- Growth factors stimulate G1 phase progression by activating calcium-permeable cation channels.
- Inhibition of these channels abrogates growth factor signaling.
- The molecular identity of these crucial channels remains largely unknown.
Purpose:
- To elucidate the molecular nature of growth factor-regulated calcium channels.
- To identify novel components involved in calcium signaling pathways.
Summary:
- Growth factors promote cell cycle progression, particularly G1 phase, through the activation of calcium-permeable cation channels.
- This activation leads to a sustained increase in intracellular calcium.
- The recent identification of the primary structure of GRC-1, a novel growth factor-regulated channel, provides a molecular target for further investigation.
Impact:
- Provides the molecular basis for understanding how growth factors regulate calcium influx.
- Opens new avenues for therapeutic interventions targeting cell cycle control.
- Enhances knowledge of calcium signaling in cell proliferation and development.
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