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Related Concept Videos

Calmodulin-dependent Signaling01:16

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Calmodulin (CaM) is a calcium-binding protein in eukaryotes that controls various calcium-regulated cellular processes. It has four calcium-binding sites that bind calcium to form the calcium-calmodulin ( Ca2+-CaM) complex. GPCR stimulation increases the calcium levels in the cells that bind to CaM and induces a conformational change.
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Calcium is an essential signaling molecule required for various cellular functions. Calcium pumps and ion channels on cell and organellar membranes, such as those on the endoplasmic reticulum (ER), regulate calcium concentrations inside the cell. They remain closed, keeping the cytosolic calcium levels low at a resting state.
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Related Experiment Video

Updated: Apr 17, 2026

Functional Calcium Imaging in Developing Cortical Networks
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Published on: October 22, 2011

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Calcium signaling in neocortical development.

Per Uhlén1, Nicolas Fritz, Erik Smedler

  • 1Department of Medical Biochemistry and Biophysics, Karolinska Institutet, SE-171 77, Stockholm, Sweden.

Developmental Neurobiology
|February 6, 2015
PubMed
Summary

Calcium signaling (Ca(2+)) is crucial for brain development, guiding neural stem cell proliferation, migration, and differentiation in the neocortex. This review highlights key findings on Ca(2+) roles in neurogenesis.

Keywords:
calcium signalingdifferentiationmigrationneocortical developmentproliferation

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Area of Science:

  • Neuroscience
  • Developmental Biology
  • Cell Signaling

Background:

  • The calcium ion (Ca(2+)) acts as a vital second messenger in neurogenesis.
  • Radial glial cells in the neocortical ventricular zone (VZ) are the primary neural stem cells.
  • Neocortical development involves precise control of cell proliferation, migration, and differentiation.

Purpose of the Study:

  • To provide a comprehensive overview of calcium signaling in neocortical development.
  • To review the impact of Ca(2+) on neural stem cell proliferation, migration, and differentiation.
  • To highlight historical and recent advancements in understanding Ca(2+) roles in neurogenesis.

Main Methods:

  • Literature review of historical and recent studies.
  • Analysis of signaling events controlling neurogenesis.
  • Examination of Ca(2+) activity in developing neocortex.

Main Results:

  • Spontaneous Ca(2+) activity is essential for fundamental cell processes during development.
  • Early neocortical development relies on gap junctions and voltage-dependent Ca(2+) channels for Ca(2+) signaling.
  • Later development involves neurotransmitters and synapses in regulating Ca(2+) activity.

Conclusions:

  • Cytosolic Ca(2+) signaling is a critical regulator of neocortical development.
  • Understanding Ca(2+) dynamics is key to deciphering the mechanisms of neurogenesis.
  • Further research on Ca(2+) signaling will elucidate complex brain structure formation.