Inhibition of placental trophoblast fusion by guanylate-binding protein 5

Syncytin-1 and Syncytin-2 are envelope glycoproteins encoded by human endogenous retroviruses that have been exapted for the fusion of cytotrophoblast cells into syncytiotrophoblasts during placental development. Pregnancy complications like preeclampsia are associated with altered expression of interferon-stimulated genes, including guanylate-binding protein 5 (GBP5). Here, we show that misdirected antiviral activity of GBP5 impairs processing and activation of Syncytin-1. In contrast, the proteolytic activation of Syncytin-2 is not affected by GBP5, and its fusogenic activity is only modestly reduced. Mechanistic analyses revealed that Syncytin-1 is mainly cleaved by the GBP5 target furin, whereas Syncytin-2 is also efficiently processed by the proprotein convertase subtilisin/kexin type 7 (PCSK7) and thus resistant to GBP5-mediated restriction. Mutational analyses mapped PCSK7 processing of Syncytin-2 to a leucine residue upstream of the polybasic cleavage site. In summary, we identified an innate immune mechanism that impairs the activity of a co-opted endogenous retroviral envelope protein during pregnancy and may potentially contribute to the pathogenesis of pregnancy disorders.

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Publication Details

Journal
Science Advances
Published
2025-05-07
DOI
https://doi.org/10.1126/sciadv.adt5388
Citations
6
Primary Topic
interferon and immune responses
Type
article
Field-Weighted Citation Impact
4.78
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article

Inhibition of placental trophoblast fusion by guanylate-binding protein 5

Oya Cingöz, Kateřina Trejbalová, Daniel Sauter, Yueshuang Lu et al.
6 citations
Science Advances
interferon and immune responses
4.78
article

Inhibition of placental trophoblast fusion by guanylate-binding protein 5

Oya Cingöz, Kateřina Trejbalová, Daniel Sauter, Yueshuang Lu, Moritz Petersen, Madhuri S. Salker, Konstantin M. J. Sparrer, Kryštof Štafl, Paul C. Stark, Rishikesh Lotke, Kenzo Tokunaga, Veronika Krchlíková, Frank Kirchhoff, Martin Trávníček, Smitha Srinivasachar Badarinarayan, Jiřı́ Hejnar, Wen Cui, Elisabeth Reith, Isabell Haußmann, Wei Wang, Claudia Baur, Johanna Weiß, Lukáš Jech, Bianca M. Fäger, Hannah Reisinger
article en
6 citations

Abstract

Syncytin-1 and Syncytin-2 are envelope glycoproteins encoded by human endogenous retroviruses that have been exapted for the fusion of cytotrophoblast cells into syncytiotrophoblasts during placental development. Pregnancy complications like preeclampsia are associated with altered expression of interferon-stimulated genes, including guanylate-binding protein 5 (GBP5). Here, we show that misdirected antiviral activity of GBP5 impairs processing and activation of Syncytin-1. In contrast, the proteolytic activation of Syncytin-2 is not affected by GBP5, and its fusogenic activity is only modestly reduced. Mechanistic analyses revealed that Syncytin-1 is mainly cleaved by the GBP5 target furin, whereas Syncytin-2 is also efficiently processed by the proprotein convertase subtilisin/kexin type 7 (PCSK7) and thus resistant to GBP5-mediated restriction. Mutational analyses mapped PCSK7 processing of Syncytin-2 to a leucine residue upstream of the polybasic cleavage site. In summary, we identified an innate immune mechanism that impairs the activity of a co-opted endogenous retroviral envelope protein during pregnancy and may potentially contribute to the pathogenesis of pregnancy disorders.

Science AdvancesVol. 11(19)
Universität Ulm (DE), German Center for Neurodegenerative Diseases (DE), National Institute of Infectious Diseases (JP), University Children's Hospital Tübingen (DE), Czech Academy of Sciences, Institute of Molecular Genetics (CZ), MRC University of Glasgow Centre for Virus Research (GB), Charité - Universitätsmedizin Berlin (DE), Chongqing Medical University (CN)
Good health and well-being
Openalex Percentile: Top 5%
interferon and immune responses
4.78
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