Secretory Nogo-B regulates Th2 differentiation in the lung cancer microenvironment
- PMID: 39083925
- DOI: 10.1016/j.intimp.2024.112763
Secretory Nogo-B regulates Th2 differentiation in the lung cancer microenvironment
Erratum in
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Corrigendum to "Secretory Nogo-B regulates Th2 differentiation in the lung cancer microenvironment" [Int. Immunopharmacol. 140 (2024) 112763].Int Immunopharmacol. 2024 Dec 5;142(Pt A):113108. doi: 10.1016/j.intimp.2024.113108. Epub 2024 Sep 16. Int Immunopharmacol. 2024. PMID: 39289042 No abstract available.
Abstract
Nogo-B, a ubiquitously expressed member of the reticulon family, plays an important role in maintaining endoplasmic reticulum (ER) structure, regulating protein folding, and calcium homeostasis. In this study, we demonstrate that Nogo-B expression and secretion are upregulated in lung cancer and correlate to overall survival. Nogo-B is secreted by various cells, particularly lung cancer cells. ER stress and phosphorylation at serine 107 can induce Nogo-B secretion. Secretory Nogo-B suppresses the differentiation of Th2 cells and the release of type 2 cytokines, thus influencing the anti-tumor effects of Th2-related immune cells, including IgE+B cell class switching and eosinophil activation.
Keywords: Endoplasmic reticulum stress; Lung cancer; Nogo-B; Secretion; Th2 cell.
Copyright © 2024 Elsevier B.V. All rights reserved.
Conflict of interest statement
Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
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