Receptor usage of Syncytin-1: ASCT2, but not ASCT1, is a functional receptor and effector of cell fusion in the human placenta
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články
Grantová podpora
LX22NPO2103
National Insitute of Virology and Bacteriology, Programme EXCELES
Praemium Academiae Award 2018
Czech Academy of Sciences
RVO 68378050-KAV-NPUI
Czech Academy of Sciences
LM2023052
Ministry of Education, Youth, and Sports of the Czech Republic
PubMed
39432789
PubMed Central
PMC11536146
DOI
10.1073/pnas.2407519121
Knihovny.cz E-zdroje
- Klíčová slova
- Syncytin-1, cell-to-cell fusion, endogenous retrovirus, placenta, viral receptor,
- MeSH
- antigeny CD98 - těžký řetězec MeSH
- fúze buněk * MeSH
- genové produkty env * metabolismus genetika MeSH
- lidé MeSH
- placenta * metabolismus MeSH
- těhotenské proteiny * metabolismus genetika MeSH
- těhotenství MeSH
- transportní systém ASC pro aminokyseliny * metabolismus genetika MeSH
- transportní systémy pro neutrální aminokyseliny metabolismus genetika MeSH
- trofoblasty metabolismus cytologie MeSH
- vedlejší histokompatibilní antigeny metabolismus genetika MeSH
- Check Tag
- lidé MeSH
- těhotenství MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- antigeny CD98 - těžký řetězec MeSH
- genové produkty env * MeSH
- SLC1A5 protein, human MeSH Prohlížeč
- SLC3A2 protein, human MeSH Prohlížeč
- syncytin MeSH Prohlížeč
- těhotenské proteiny * MeSH
- transportní systém ASC pro aminokyseliny * MeSH
- transportní systémy pro neutrální aminokyseliny MeSH
- vedlejší histokompatibilní antigeny MeSH
Syncytin-1, a human fusogenic protein of retroviral origin, is crucial for placental syncytiotrophoblast formation. To mediate cell-to-cell fusion, Syncytin-1 requires specific interaction with its cognate receptor. Two trimeric transmembrane proteins, Alanine, Serine, Cysteine Transporters 1 and 2 (ASCT1 and ASCT2), were suggested and widely accepted as Syncytin-1 cellular receptors. To quantitatively assess the individual contributions of human ASCT1 and ASCT2 to the fusogenic activity of Syncytin-1, we developed a model system where the ASCT1 and ASCT2 double knockout was rescued by ectopic expression of either ASCT1 or ASCT2. We demonstrated that ASCT2 was required for Syncytin-1 binding, cellular entry, and cell-to-cell fusion, while ASCT1 was not involved in this receptor interaction. We experimentally validated the ASCT1-ASCT2 heterotrimers as a possible explanation for the previous misidentification of ASCT1 as a receptor for Syncytin-1. This redefinition of receptor specificity is important for proper understanding of Syncytin-1 function in normal and pathological pregnancy.
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