Evidence map›Paper›PMID 39102426›Full record

ArticlePLoS pathogens2024

SARS-CoV-2 spike-induced syncytia are senescent and contribute to exacerbated heart failure.

Huilong Li, Luming Wan, Muyi Liu, Enhao Ma, Linfei Huang, Yilong Yang, Qihong Li, Yi Fang, Jingfei Li, Bingqing Han and 20 more

Abstract read
In one paragraph

Article in PLoS pathogens, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

30 authors.

Huilong LiBeijing Institute of Biotechnology, Beijing, China.
Luming WanBeijing Institute of Biotechnology, Beijing, China.
Muyi LiuBeijing Institute of Biotechnology, Beijing, China.
Enhao MaTsinghua-Peking Center for Life Sciences, School of Medicine, Tsinghua University, Beijing, China.
Linfei HuangBeijing Institute of Biotechnology, Beijing, China.
Yilong YangBeijing Institute of Biotechnology, Beijing, China.
Qihong LiThe Fifth Medical Centre, Chinese PLA General Hospital, Beijing, China.
Yi FangThe Fifth Medical Centre, Chinese PLA General Hospital, Beijing, China.
Jingfei LiBeijing Institute of Biotechnology, Beijing, China.
Bingqing HanBeijing Institute of Biotechnology, Beijing, China.
Chang ZhangBeijing Institute of Biotechnology, Beijing, China.
Lijuan SunBeijing Yaogen Biotechnology Co.Ltd, Beijing, China.
Xufeng HouBeijing Yaogen Biotechnology Co.Ltd, Beijing, China.
Haiyang LiBeijing Anzhen Hospital, Capital Medical University, Beijing, China.
Mingyu SunBeijing Anzhen Hospital, Capital Medical University, Beijing, China.
Sichong QianBeijing Anzhen Hospital, Capital Medical University, Beijing, China.
Xuejing DuanDepartment of Pathology, Fuwai Hospital, Peking Union Medical College, Chinese Academy of Medical Science, Beijing, China.
Ruzhou ZhaoBeijing Institute of Biotechnology, Beijing, China.
Xiaopan YangBeijing Institute of Biotechnology, Beijing, China.
Yi ChenBeijing Institute of Biotechnology, Beijing, China.
Shipo WuBeijing Institute of Biotechnology, Beijing, China.
Xuhui ZhangBeijing Yaogen Biotechnology Co.Ltd, Beijing, China.
Yanhong ZhangBeijing Institute of Biotechnology, Beijing, China.
Gong ChengTsinghua-Peking Center for Life Sciences, School of Medicine, Tsinghua University, Beijing, China.
Gengye ChenPeople's Hospital of Ningxia Hui Autonomous Region, Yinchuan, China.
Qi GaoBeijing Yaogen Biotechnology Co.Ltd, Beijing, China.
Junjie XuBeijing Institute of Biotechnology, Beijing, China.
Lihua HouBeijing Institute of Biotechnology, Beijing, China.
Congwen WeiBeijing Institute of Biotechnology, Beijing, China.
Hui ZhongBeijing Institute of Biotechnology, Beijing, China.ORCID 0000-0003-2128-9686

Funding

Development Program of China 2022YFC3600100National Natural Science Foundation of China 32070755National Natural Science Foundation of China 32100558National Natural Science Foundation of China 32270823National Natural Science Foundation of China 32370178National Natural Science Foundation of China 82070595
6 · The paper itself

Abstract

SARS-CoV-2 spike protein (SARS-2-S) induced cell-cell fusion in uninfected cells may occur in long COVID-19 syndrome, as circulating SARS-2-S or extracellular vesicles containing SARS-2-S (S-EVs) were found to be prevalent in post-acute sequelae of COVID-19 (PASC) for up to 12 months after diagnosis. Although isolated recombinant SARS-2-S protein has been shown to increase the SASP in senescent ACE2-expressing cells, the direct linkage of SARS-2-S syncytia with senescence in the absence of virus infection and the degree to which SARS-2-S syncytia affect pathology in the setting of cardiac dysfunction are unknown. Here, we found that the senescent outcome of SARS-2-S induced syncytia exacerbated heart failure progression. We first demonstrated that syncytium formation in cells expressing SARS-2-S delivered by DNA plasmid or LNP-mRNA exhibits a senescence-like phenotype. Extracellular vesicles containing SARS-2-S (S-EVs) also confer a potent ability to form senescent syncytia without de novo synthesis of SARS-2-S. However, it is important to note that currently approved COVID-19 mRNA vaccines do not induce syncytium formation or cellular senescence. Mechanistically, SARS-2-S syncytia provoke the formation of functional MAVS aggregates, which regulate the senescence fate of SARS-2-S syncytia by TNFα. We further demonstrate that senescent SARS-2-S syncytia exhibit shrinked morphology, leading to the activation of WNK1 and impaired cardiac metabolism. In pre-existing heart failure mice, the WNK1 inhibitor WNK463, anti-syncytial drug niclosamide, and senolytic dasatinib protect the heart from exacerbated heart failure triggered by SARS-2-S. Our findings thus suggest a potential mechanism for COVID-19-mediated cardiac pathology and recommend the application of WNK1 inhibitor for therapy especially in individuals with post-acute sequelae of COVID-19.

Indexed as

Cellular SenescenceCOVID-19Giant CellsHeart FailureSARS-CoV-2Spike Glycoprotein, CoronavirusAnimalsExtracellular VesiclesHumansMiceSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2

Identifiers

PMID39102426
PMCPMC11326701

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.