Activation of lysophagy by a TBK1-SCFFBXO3-TMEM192-TAX1BP1 axis in response to lysosomal damage

• Published in: Nature communications 2025-01, Vol.16 (1), p.1109
• Main Authors: Park, Na Yeon, Jo, Doo Sin, Yang, Jae-Yoon, Bae, Ji-Eun, Kim, Joon Bum, Kim, Yong Hwan, Kim, Seong Hyun, Kim, Pansoo, Lee, Dong-Seok, Yoshimori, Tamotsu, Jo, Eun-Kyeong, Yeom, Eunbyul, Cho, Dong-Hyung
• Format: Article
• Language: English
• Subjects: 13/1; 13/109; 13/89; 14; 14/19; 42/70; 45; 49; 631/337/458/582; 631/80/39; 631/80/642/1624; 631/80/86/2366; Damage detection; Homeostasis; Humanities and Social Sciences; Integrity; L-leucine methyl ester; Leucine; Lysosomes; multidisciplinary; Regulatory mechanisms (biology); Science; Science (multidisciplinary); Ubiquitin-protein ligase; Ubiquitination
• ISSN: 2041-1723; 2041-1723
• DOI: 10.1038/s41467-025-56294-y

Lysophagy eliminates damaged lysosomes and is crucial to cellular homeostasis; however, its underlying mechanisms are not entirely understood. We screen a ubiquitination-related compound library and determine that the substrate recognition component of the SCF-type E3 ubiquitin ligase complex, SCF FBXO3 (FBXO3), which is a critical lysophagy regulator. Inhibition of FBXO3 reduces lysophagy and lysophagic flux in response to L-leucyl-L-leucine methyl ester (LLOMe). Furthermore, FBXO3 interacts with TMEM192, leading to its ubiquitination in LLOMe-treated cells. We also identify TAX1BP1 as a critical autophagic adaptor that recognizes ubiquitinated TMEM192 during lysophagy and find that TBK1 activation is crucial for lysophagy, as it phosphorylates FBXO3 in response to lysosomal damage. Knockout of FBXO3 significantly impairs lysophagy, and its reconstitution with a loss-of-function mutant (V221I) further confirms its essential role in lysophagy regulation. Collectively, our findings highlight the significance of the TBK1-FBXO3-TMEM192-TAX1BP1 axis in lysophagy and emphasize the critical role of FBXO3 in lysosomal integrity. Damaged lysosomes are eliminated by lysophagy, yet the regulatory mechanisms of this process are not fully defined. Here, the authors identify that the TBK1-SCFFBXO3-TMEM192-TAX1BP1 axis is essential for lysosome degradation, with FBXO3 functioning in lysosome integrity.