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Tetraspanin 3: A central endocytic membrane component regulating the expression of ADAM10, presenilin and the amyloid precursor protein
L. Seipold, M. Damme, J. Prox, B. Rabe, P. Kasparek, R. Sedlacek, H. Altmeppen, M. Willem, B. Boland, M. Glatzel, P. Saftig,
Jazyk angličtina Země Nizozemsko
Typ dokumentu časopisecké články, práce podpořená grantem
- MeSH
- amyloidový prekurzorový protein beta genetika metabolismus MeSH
- buněčná membrána metabolismus MeSH
- endocytóza MeSH
- endozomy chemie metabolismus MeSH
- HEK293 buňky MeSH
- kadheriny genetika metabolismus MeSH
- lidé MeSH
- membránové proteiny genetika metabolismus MeSH
- mozek - chemie MeSH
- mozek metabolismus MeSH
- myši MeSH
- nádorové buněčné linie MeSH
- neurony cytologie metabolismus MeSH
- preseniliny genetika metabolismus MeSH
- protein ADAM10 genetika metabolismus MeSH
- proteiny nervové tkáně genetika metabolismus MeSH
- receptory Notch genetika metabolismus MeSH
- regulace genové exprese MeSH
- sekretasy genetika metabolismus MeSH
- signální transdukce MeSH
- techniky dvojhybridového systému MeSH
- tetraspaniny genetika metabolismus MeSH
- transport proteinů MeSH
- vazba proteinů MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Despite existing knowledge about the role of the A Disintegrin and Metalloproteinase 10 (ADAM10) as the α-secretase involved in the non-amyloidogenic processing of the amyloid precursor protein (APP) and Notch signalling we have only limited information about its regulation. In this study, we have identified ADAM10 interactors using a split ubiquitin yeast two hybrid approach. Tetraspanin 3 (Tspan3), which is highly expressed in the murine brain and elevated in brains of Alzheimer´s disease (AD) patients, was identified and confirmed to bind ADAM10 by co-immunoprecipitation experiments in mammalian cells in complex with APP and the γ-secretase protease presenilin. Tspan3 expression increased the cell surface levels of its interacting partners and was mainly localized in early and late endosomes. In contrast to the previously described ADAM10-binding tetraspanins, Tspan3 did not affect the endoplasmic reticulum to plasma membrane transport of ADAM10. Heterologous Tspan3 expression significantly increased the appearance of carboxy-terminal cleavage products of ADAM10 and APP, whereas N-cadherin ectodomain shedding appeared unaffected. Inhibiting the endocytosis of Tspan3 by mutating a critical cytoplasmic tyrosine-based internalization motif led to increased surface expression of APP and ADAM10. After its downregulation in neuroblastoma cells and in brains of Tspan3-deficient mice, ADAM10 and APP levels appeared unaltered possibly due to a compensatory increase in the expression of Tspans 5 and 7, respectively. In conclusion, our data suggest that Tspan3 acts in concert with other tetraspanins as a stabilizing factor of active ADAM10, APP and the γ-secretase complex at the plasma membrane and within the endocytic pathway.
Biomedical Center Ludwig Maximilians University 81337 Munich Germany
Department of Pharmacology and Therapeutics School of Medicine University College Cork Cork Ireland
Institute of Neuropathology University Medical Center Hamburg Eppendorf Hamburg Germany
Citace poskytuje Crossref.org
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