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Published on: January 7, 2019
Interleukin 24: Signal Transduction Pathways
Simira Smith1, Sual Lopez1, Anastassiya Kim2
1Department of Biological Sciences, Herbert H. Lehman College, City University of New York, 250 Bedford Park Boulevard West, Bronx, NY 10468, USA.
Insights
Interleukin 24 (IL-24) has vital roles in immunity and inflammation. This review details IL-24
Area of Science:
- Immunology
- Molecular Biology
- Cell Biology
Background:
- Interleukin 24 (IL-24), part of the IL-10 family, is involved in antitumor responses, immune regulation, and inflammation.
- IL-24 is produced by various cell types and signals through canonical and noncanonical pathways.
- Understanding IL-24 signaling is crucial for therapeutic targeting.
Purpose of the Study:
- To review the canonical and noncanonical signaling pathways of Interleukin 24.
- To highlight the molecular interactions involved in IL-24 signal transduction.
- To provide insights into the therapeutic potential of targeting IL-24.
Main Methods:
- Literature review of studies on Interleukin 24 signaling.
- Analysis of canonical JAK/STAT and noncanonical pathways.
- Discussion of IL-24 interactions with receptors and intracellular proteins.
Main Results:
- Canonical IL-24 signaling involves IL-20 receptors and JAK/STAT activation.
- Noncanonical pathways include interactions with Protein Kinase R, mitochondrial proteins, and Sigma 1 Receptor.
- Both canonical and noncanonical pathways contribute to IL-24's diverse functions.
Conclusions:
- IL-24 utilizes complex and diverse signaling mechanisms.
- Further elucidation of these pathways is essential for developing IL-24-based therapies.
- Targeting IL-24 signaling holds promise for treating various diseases.
Abstract:
Interleukin 24 is a member of the IL-10 family with crucial roles in antitumor, wound healing responses, host defense, immune regulation, and inflammation. Interleukin 24 is produced by both immune and nonimmune cells. Its canonical pathway relies on recognition and interaction with specific Interleukin 20 receptors in the plasma membrane and subsequent cytoplasmic Janus protein tyrosine kinases (JAK)/signal transducer and activator of the transcription (STAT) activation. The identification of noncanonical JAK/STAT-independent signaling pathways downstream of IL-24 relies on the interaction of IL-24 with protein kinase R in the cytosol, respiratory chain proteins in the inner mitochondrial membrane, and chaperones such as Sigma 1 Receptor in the endoplasmic reticulum. Numerous studies have shown that enhancing or inhibiting the expression of Interleukin 24 has a therapeutic effect in animal models and clinical trials in different pathologies. Successful drug targeting will require a deeper understanding of the downstream signaling pathways. In this review, we discuss the signaling pathway triggered by IL-24.
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