Autophagy-independent role of ATG9A vesicles as carriers for galectin-9 secretion
Galectins play vital roles in cellular processes such as adhesion, communication, and survival, yet the mechanisms underlying their unconventional secretion remain poorly understood. This study identifies ATG9A, a core autophagy protein, as a key regulator of galectin-9 secretion via a mechanism independent of classical autophagy, secretory autophagy, or the LC3-dependent extracellular vesicle loading and secretion pathway. ATG9A vesicles function as specialized carriers, with the N-terminus of ATG9A and both carbohydrate recognition domains of galectin-9 being critical for the process. TMED10 mediates the incorporation of galectin-9 into ATG9A vesicles, which then fuse with the plasma membrane via the STX13-SNAP23-VAMP3 SNARE complex. Furthermore, ATG9A regulates the secretion of other proteins, including galectin-4, galectin-8, and annexin A6, but not IL-1β, galectin-3, or FGF2. This mechanism is potentially conserved across other cell types, including monocytic cells, which underscores its broader significance in unconventional protein secretion.
Authors
- Cuicui Ji (ORCID: https://orcid.org/0000-0001-7764-6422)
- Xuechai Chen (ORCID: https://orcid.org/0000-0001-8539-451X)
- Wei Jiang (ORCID: https://orcid.org/0000-0003-1591-4721)
- Yunpeng Zhao (ORCID: https://orcid.org/0000-0001-8996-7813)
- Meiling Wu (ORCID: https://orcid.org/0000-0002-2654-4896)
- Juan Wang
- Wenting Zhang (ORCID: https://orcid.org/0000-0002-8550-8086)
- Xianghua Li (ORCID: https://orcid.org/0000-0002-2172-7271)
- Jian Li (ORCID: https://orcid.org/0000-0003-2131-321X)
- Yukun Liu
- Haolin Zhang (ORCID: https://orcid.org/0000-0001-8980-0626)
- Xiaoli Wang (ORCID: https://orcid.org/0000-0002-2192-5374)
- Tianlong He
Institutions
- Shandong University (CN)
- Beijing University of Technology (CN)
Publication Details
- Journal
- Nature Communications
- Published
- 2025-05-07
- DOI
- https://doi.org/10.1038/s41467-025-59605-5
- Citations
- 6
- Primary Topic
- Galectins and Cancer Biology
- Type
- article
- Field-Weighted Citation Impact
- 4.78
Funders
- National Natural Science Foundation of China
- Chinese Academy of Sciences
- Tsinghua University
- Institute of Biophysics, Chinese Academy of Sciences