Abstract
SQSTM1/p62 droplets play crucial roles in droplets-based macroautophagy/autophagy including selective autophagy and bulk autophagy. We observed that under several stress milieus, SQSTM1 droplets entirely colocalize with P-body markers, and these stress-induced SQSTM1 droplets contain mRNAs. We thus determined that under certain stress conditions, autophagic SQSTM1 droplets are converted to a type of enlarged P-bodies, designated SQSTM1/p62-dependent P-bodies (pd-PBs). Stress-enhanced SQSTM1 droplet formation drives the nucleation of pd-PBs through the interaction between SQSTM1 and the RNA-binding protein DDX6. Furthermore, pd-PBs sequester PYCARD, facilitating the assembly of NLRP3 inflammasomes, and in turn induce inflammation-related cytotoxicity. Our study suggests that under stress settings, autophagic SQSTM1 droplets are transformed to pd-PBs, underlining a critical role of SQSTM1 in P-body condensation.
| Original language | English |
|---|---|
| Pages (from-to) | 2100-2101 |
| Number of pages | 2 |
| Journal | Autophagy |
| Volume | 20 |
| Issue number | 9 |
| Early online date | 10 Apr 2024 |
| DOIs | |
| Publication status | Published - Sept 2024 |
ASJC Scopus subject areas
- Molecular Biology
- Cell Biology
Keywords
- Autophagy
- NLRP3 inflammasome
- P-bodies
- PYCARD
- SQSTM1
- Sequestosome-1 Protein/metabolism
- Animals
- Inflammasomes/metabolism
- Autophagy/physiology
- Humans
- Mice
- DEAD-box RNA Helicases/metabolism