CLN3 mediates chloride efflux from lysosomes
Neurodegenerative diseases, which pose significant challenges for effective treatment, often involve risk variants of lysosomal gene products that disrupt lysosomal function, leading to the accumulation of indigestible materials and damage to brain cells. The lysosome is a degradative organelle and a signaling hub that senses nutrient availability. How lysosomal dysfunction contributes to neurodegenerative diseases is an important open question. In this study, we identified CLN3 (ceroid lipofuscinosis, neuronal 3), an endolysosomal protein that is linked to Batten disease, as an evolutionarily conserved protein that facilitates lysosomal chloride efflux. Additionally, we report that a natural compound with anti-inflammatory properties-the curcumin analog C1, which is a TFEB (transcription factor EB) activator-could enhance CLN3 activity and improve lysosomal function. These findings provide new insight into the role of CLN3 in lysosomal ion homeostasis and raise the possibility that modulation of the TFEB-CLN3 signaling axis may hold therapeutic potential for lysosomal storage disorders.
Authors
- Marena Tynan-La Fontaine
- Lily Yeh Jan (ORCID: https://orcid.org/0000-0003-3938-8498)
- Yayu Wang (ORCID: https://orcid.org/0000-0003-3976-3817)
- Adeline J. H. Yong (ORCID: https://orcid.org/0000-0001-8605-3637)
- Y. N. Jan
- Xiaofan Zhang (ORCID: https://orcid.org/0000-0003-1025-164X)
- Chao Chen (ORCID: https://orcid.org/0000-0001-9518-4858)
- Kai Li (ORCID: https://orcid.org/0000-0002-3382-1679)
- Wei Chen
Institutions
- Howard Hughes Medical Institute (US)
- University of California, San Francisco (US)
- University of California San Francisco Medical Center (US)
Publication Details
- Journal
- Neuron
- Published
- 2026-01-19
- DOI
- https://doi.org/10.1016/j.neuron.2025.11.013
- Primary Topic
- Lysosomal Storage Disorders Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00