While primarily found in endo-lysosomal compartments, the cysteine protease legumain can also translocate to the cell surface if stabilized by the interaction with the RGD-dependent integrin receptor αVβ3. Previously, it has been shown that legumain expression is inversely related to BDNF-TrkB activity. Here we show that legumain can conversely act on TrkB-BDNF by processing the C-terminal linker region of the TrkB ectodomain in vitro. Importantly, when in complex with BDNF, TrkB was not cleaved by legumain. Legumain-processed TrkB was still able to bind BDNF, suggesting a potential scavenger function of soluble TrkB towards BDNF. The work thus presents another mechanistic link explaining the reciprocal TrkB signaling and δ-secretase activity of legumain, with relevance for neurodegeneration.
Legumain Functions as a Transient TrkB Sheddase
C. Holzner,Katharina Böttinger,C. Blöchl,C. Huber,S. Dahms,E. Dall,H. Brandstetter
Published 2023 in International Journal of Molecular Sciences
ABSTRACT
PUBLICATION RECORD
- Publication year
2023
- Venue
International Journal of Molecular Sciences
- Publication date
2023-03-01
- Fields of study
Biology, Medicine
- Identifiers
- External record
- Source metadata
Semantic Scholar, PubMed
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