FGF13 is not secreted from mouse neurons
FGF13, a noncanonical fibroblast growth factor (FGF) and member of the fibroblast growth factor homologous factor (FHF) subset, lacks a signal sequence and was previously reported to remain intracellular, where it regulates voltage-gated sodium channels (VGSCs) at least in part through direct interaction with the cytoplasmic C-terminus of VGSCs. Recent reports suggest FGF13 is secreted and regulates neuronal VGSCs through interactions with extracellular domains of integral plasma membrane proteins, yet supportive data are limited. Using rigorous positive and negative controls, we show that transfected FGF13 is not secreted from cultured cells in a heterologous expression system, nor is endogenous FGF13 secreted from cultured neurons. Furthermore, using multiple unbiased screens including proximity labeling proteomics, our results suggest FGF13 remains within membranes and is unavailable to interact directly with extracellular protein domains.
Authors
- Mattia Malvezzi (ORCID: https://orcid.org/0000-0003-2181-7522)
- Geoffrey S. Pitt (ORCID: https://orcid.org/0000-0003-2246-0289)
- David Lyden (ORCID: https://orcid.org/0000-0003-0193-4131)
- Steven O. Marx (ORCID: https://orcid.org/0000-0002-0577-6030)
- Patrick Towers
- Haiying Zhang (ORCID: https://orcid.org/0000-0002-7158-2373)
Institutions
- Cornell University (US)
- Cardiovascular Institute Hospital (JP)
- Children's Cancer and Blood Foundation (US)
- Weill Cornell Medicine (US)
- Columbia University (US)
Publication Details
- Journal
- JCI Insight
- Published
- 2025-11-25
- DOI
- https://doi.org/10.1172/jci.insight.195998
- Primary Topic
- Fibroblast Growth Factor Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Institutes of Health
- National Cancer Institute