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Related Concept Videos

Calmodulin-dependent Signaling01:16

Calmodulin-dependent Signaling

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.
The Ca2+-CaM complex does not have enzymatic activity by itself. Instead, the complex binds downstream target proteins, including membrane proteins or enzymes,...
Feedback Regulation of Calcium Concentration01:27

Feedback Regulation of Calcium Concentration

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.
Various transmembrane receptors, such as G protein-coupled receptors (GPCRs), elicit a response to extracellular signals by increasing cytosolic calcium. Activated GPCRs...
Immunoglobulin-like Cell Adhesion Molecules01:31

Immunoglobulin-like Cell Adhesion Molecules

Immunoglobulin-like cell adhesion molecules or Ig-CAMs are a versatile group of cell surface glycoproteins belonging to the immunoglobulin protein superfamily. Ig-CAMs possess the characteristic immunoglobulin protein domains and other domains such as the fibronectin type III domain. The Ig domains are glycosylated to varying degrees in different Ig-CAMs.
Ig-CAMs exhibit either homophilic binding (to other Ig-CAMs) or heterophilic binding (to other ligands such as integrins). While most Ig-CAMs...
NF-κB-dependent Signaling Pathway02:26

NF-κB-dependent Signaling Pathway

The transcription factor NF-κB was discovered in 1986 in the lab of Nobel laureate Professor David Baltimore, for its interaction with the immunoglobulin light chain enhancer in B-cells. After more than three decades of study, it is now evident that NF-κB regulates the expression of over 100 genes. Most of these genes play an essential role in the innate and adaptive immune responses as well as the inflammatory responses of animals.
NF-κB-dependent Signaling Mechanism
The heterodimer of NF-κB...
Amplifying Signals via Second Messengers01:15

Amplifying Signals via Second Messengers

Many receptor binding ligands are hydrophilic; they do not cross the cell membrane but bind to cell-surface receptors. Thus, their message must be relayed by second messengers present in the cell cytoplasm. There are several second messenger pathways, each with its own way of relaying information. For example, the G protein-coupled receptors can activate both phosphoinositol and cyclic AMP (cAMP) second messenger pathways. The phosphoinositol pathway is active when the receptor induces...
Skeleton and Calcium Homeostasis01:21

Skeleton and Calcium Homeostasis

Calcium is not only the most abundant mineral in bone but also the most abundant mineral in the human body. Calcium ions are needed for bone mineralization, tooth health, heart rate regulation and strength of contraction, blood coagulation, the contraction of smooth and skeletal muscle cells, and the regulation of nerve impulse conduction. The average calcium level in the blood is about 10 mg/dL. When the body cannot maintain this level, a person will experience hypo or hypercalcemia.

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Related Experiment Video

Updated: Jun 27, 2026

Imaging Initial Ca2+ Microdomains in Primary T Cells
05:56

Imaging Initial Ca2+ Microdomains in Primary T Cells

Published on: October 4, 2024

Calcium signaling in immune cells.

Monika Vig1, Jean-Pierre Kinet

  • 1Laboratory of Allergy and Immunology, Department of Pathology, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts 02115, USA. mvig@bidmc.harvard.edu

Nature Immunology
|December 18, 2008
PubMed
Summary

Calcium signaling is crucial in lymphocytes, with store-operated calcium (SOC) channels mediating calcium influx. Recent discoveries of CRACM1 and STIM1 advance understanding of this vital pathway.

Area of Science:

  • Immunology
  • Cell Biology
  • Biochemistry

Background:

  • Calcium ions (Ca2+) function as critical second messengers in diverse cell types, including lymphocytes.
  • Lymphocytes maintain a low intracellular Ca2+ concentration at rest.
  • Antigen receptor engagement triggers Ca2+ influx into lymphocytes via multiple pathways.

Purpose of the Study:

  • To review recent advancements in understanding calcium (Ca2+) signaling in lymphocytes.
  • To emphasize the role and mechanisms of store-operated calcium (SOC) channels in lymphocyte activation.
  • To identify current challenges and future research directions in the field.

Main Methods:

  • Literature review focusing on calcium signaling and SOC channels in lymphocytes.
  • Discussion of molecular components like CRACM1 and STIM1.

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Analysis of T-cell Receptor-Induced Calcium Influx in Primary Murine T-cells by Full Spectrum Flow Cytometry
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Last Updated: Jun 27, 2026

Imaging Initial Ca2+ Microdomains in Primary T Cells
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Analysis of T-cell Receptor-Induced Calcium Influx in Primary Murine T-cells by Full Spectrum Flow Cytometry
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Analysis of T-cell Receptor-Induced Calcium Influx in Primary Murine T-cells by Full Spectrum Flow Cytometry

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  • Analysis of genetic and molecular manipulation studies.
  • Main Results:

    • Store-operated calcium (SOC) channels are a primary route for Ca2+ entry in lymphocytes.
    • The identification of CRACM1 (pore subunit) and STIM1 (calcium sensor) has enabled detailed study of SOC entry.
    • Advances in understanding the molecular basis of SOC channel function.

    Conclusions:

    • Significant progress has been made in elucidating Ca2+ signaling pathways in lymphocytes, particularly SOC entry.
    • The molecular players CRACM1 and STIM1 are central to SOC channel function.
    • Further research is needed to fully address outstanding questions and explore future therapeutic avenues.