# Viewing Inflammation and Immunoregulation Under the Calpain System Lens

**Authors:** Vijay Kumar, John H. Stewart

PMC · DOI: 10.3390/cells14221814 · 2025-11-19

## TL;DR

The paper explores how calpain-1 and calpain-2 proteases influence immune responses and inflammation, emphasizing their role in immune regulation and disease.

## Contribution

It provides a comprehensive overview of calpain-1 and calpain-2's roles in innate and adaptive immune cells under inflammatory conditions.

## Key findings

- Calpain-1 and calpain-2 are activated during inflammation and impact immune cell functions.
- Dysregulation of calpains may contribute to inflammation-associated diseases.
- Understanding calpain activity could lead to better inflammation resolution strategies.

## Abstract

The controlled pro-inflammatory immune response is critical for fighting against external and endogenous threats, such as microbes/pathogens, allergens, xenobiotics, various antigens, and dying host cells and their mediators (DNA, RNA, and nuclear proteins) released into the circulation and cytosol (PAMPs, MAMPs, and DAMPs). Several pattern recognition receptors (PRRs) and their downstream adaptor molecules, expressed by innate and adaptive immune cells, are critical in generating the inflammatory immune response by recognizing PAMPs, MAMPs, and DAMPs. However, their dysregulation may predispose the host to develop inflammation-associated organ damage, neurodegeneration, autoimmunity, cancer, and even death due to the absence of the inflammation resolution phase. The cytosolic calcium (Ca2+) level regulates the survival, proliferation, and immunological functions of immune cells. Cysteine-rich proteases, specifically calpains, are Ca2+-dependent proteases that become activated during inflammatory conditions, playing a critical role in the inflammatory process and associated organ damage. Therefore, this article discusses the expression and function of calpain-1 and calpain-2 (ubiquitous calpains) in various innate (epithelial, endothelial, dendritic, mast, and NK cells, as well as macrophages) and adaptive (T and B cells) immune cells, affecting inflammation and immune regulation. As inflammatory diseases are on the rise due to several factors, such as environment, lifestyle, and an aging population, we must not just investigate but strive for a deeper understanding of the inflammation and immunoregulation under the calpain system (calpain-1 and calpain-2 and their endogenous negative regulator calpastatin) lens, which is ubiquitous and senses cytosolic Ca2+ changes to impact immune response.

## Linked entities

- **Genes:** LOC104918347 (calpain-1 catalytic subunit) [NCBI Gene 104918347], LOC104934896 (calpain-2 catalytic subunit) [NCBI Gene 104934896], cast.L (calpastatin L homeolog) [NCBI Gene 398117]
- **Proteins:** LOC104918347 (calpain-1 catalytic subunit), LOC104934896 (calpain-2 catalytic subunit), cast.L (calpastatin L homeolog)
- **Chemicals:** Ca2+ (PubChem CID 271)
- **Diseases:** cancer (MONDO:0004992)

## Full-text entities

- **Genes:** CAPN2 (calpain 2) [NCBI Gene 824] {aka CANP2, CANPL2, CANPml, mCANP}, CAST (calpastatin) [NCBI Gene 831] {aka BS-17, MIR583HG, PLACK}, CAPN1 (calpain 1) [NCBI Gene 823] {aka CANP, CANP1, CANPL1, SPG76, muCANP, muCL}
- **Diseases:** autoimmunity (MESH:D001327), Inflammation (MESH:D007249), neurodegeneration (MESH:D019636), organ damage (MESH:D000092124), cancer (MESH:D009369), death (MESH:D003643)
- **Chemicals:** calcium (MESH:D002118), Ca2+ (-)

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12650998/full.md

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Source: https://tomesphere.com/paper/PMC12650998