Am J Respir Cell Mol Biol. 2025 Feb 25. doi: 10.1165/rcmb.2024-0191OC. Online ahead of print.
ABSTRACT
Lysosomal dysfunction is the primary cause of various immune disorders. Transcription factor EB (TFEB) SUMOylation is critically involved in the lysosomal biogenesis. Whether TFEB SUMOylation-associated lysosomal dysfunction contributes to asthma pathogenesis remain to be determined. Here, we observed that ovalbumin (OVA)-stimulation impaired lysosomal function through TFEB SUMOylation, which leads to increased NLRP3 and inflammatory factors. Mechanistically, mutation of TFEB SUMOylation site did not abolish the ability of its nuclear translocation, but increased TFEB stability and binding capability with target genes’ promoters, thereby promoting lysosomal biogenesis and bioactivity through liquid-liquid phase separation (LLPS), and thus inhibiting the production of inflammatory factors and alleviating allergic airway inflammation. Our observations demonstrate that TFEB SUMOylation interferes with lysosomal biogenesis contributing to asthma pathogenesis, lending mechanistic insight into asthmatic disease and improving our understanding of the transcriptional regulation of host immune responses.
PMID:39998815 | DOI:10.1165/rcmb.2024-0191OC
