Nemo mRNA vaccination improves airway barrier function in mice with airway allergy
Epithelial barrier dysfunction plays an important role in the pathogenesis of Th2 bias. The mechanism requires further clarification. NEMO is associated with regulating apoptotic activities in the cell. The purpose of this study is to investigate the role of insufficient Nemo signals in developing T...
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Veröffentlicht in: | Cellular signalling 2024-09, Vol.121, p.111257, Article 111257 |
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Sprache: | eng |
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Zusammenfassung: | Epithelial barrier dysfunction plays an important role in the pathogenesis of Th2 bias. The mechanism requires further clarification. NEMO is associated with regulating apoptotic activities in the cell. The purpose of this study is to investigate the role of insufficient Nemo signals in developing Th2 bias in the respiratory tract. Nemof/fEpcam-Cre mice (A mouse strain carrying NEMO-deficient epithelial cells. NemoKO mice, in short) was generated. An airway Th2 bias mouse model was established with the ovalbumin/alum protocol. The NemoKO mice exhibited spontaneous airway Th2 bias. Respiratory tract epithelial barrier integrity was compromised in NemoKO mice. Apoptosis was found in approximately 10% of the epithelial cells of the respiratory tract in NemoKO mice. The reconstruction of the Nemo expression restored homeostasis within the epithelial barrier of the airways. Restoration of Nemo gene expression in epithelial cells by Nemo mRNA vaccination alleviated Th2 bias in mice with airway allergy. To sum up, NEMO plays an important role in maintaining the integrity of the epithelial barrier in the respiratory tract. Administration of NEMO mRNA vaccines can restore epithelial barrier functions and alleviate Th2 bias in the airways.
•NemoKO mice exhibited spontaneous airway Th2 bias.•Respiratory tract epithelial barrier integrity was compromised in NemoKO mice.•Apoptosis was found in respiratory tract in NemoKO mice.•Reconstruction of Nemo restored homeostasis of airway epithelial barrier. |
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ISSN: | 0898-6568 1873-3913 1873-3913 |
DOI: | 10.1016/j.cellsig.2024.111257 |