Evidence map›Paper›PMID 37416931›Full record

ArticleImmune network2023

SARS-CoV-2 Infection Induces HMGB1 Secretion Through Post-Translational Modification and PANoptosis.

Man Sup Kwak, Seoyeon Choi, Jiseon Kim, Hoojung Lee, In Ho Park, Jooyeon Oh, Duong Ngoc Mai, Nam-Hyuk Cho, Ki Taek Nam, Jeon-Soo Shin

Open access · diamondAbstract read
In one paragraph

Article in Immune network, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
4.4field-weighted citation impact, top 5% of its field
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

19 citing papers in PubMed, 23 citations in OpenAlex.

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  7. Involvement of the pyroptosis-HMGB1 axis in systemic diseases.Frontiers in cell and developmental biology · 2026
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  17. The lactate metabolism and protein lactylation in epilepsy.Frontiers in cellular neuroscience · 2024
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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

10 authors at 2 institutions in 2 countries.

Man Sup KwakDepartment of Microbiology, Yonsei University College of Medicine, Seoul 03722, Korea.ORCID https://orcid.org/0000-0002-3989-3016
Seoyeon ChoiDepartment of Microbiology, Yonsei University College of Medicine, Seoul 03722, Korea.ORCID https://orcid.org/0000-0002-3974-2453
Jiseon KimBrain Korea 21 FOUR Project for Medical Science, Yonsei University College of Medicine, Seoul 03722, Korea.ORCID https://orcid.org/0000-0002-0979-0278
Hoojung LeeDepartment of Microbiology, Yonsei University College of Medicine, Seoul 03722, Korea.ORCID https://orcid.org/0000-0002-3471-2685
In Ho ParkInstitute for Immunology and Immunological Diseases, Yonsei University College of Medicine, Seoul 03722, Korea.ORCID https://orcid.org/0000-0003-2190-5469
Jooyeon OhDepartment of Microbiology, Yonsei University College of Medicine, Seoul 03722, Korea.ORCID https://orcid.org/0000-0003-1701-7792
Duong Ngoc MaiDepartment of Microbiology, Yonsei University College of Medicine, Seoul 03722, Korea.ORCID https://orcid.org/0000-0002-6217-604X
Nam-Hyuk ChoDepartment of Microbiology and Immunology, Seoul National University College of Medicine, Seoul 03080, Korea.ORCID https://orcid.org/0000-0003-3673-6397
Ki Taek NamBrain Korea 21 FOUR Project for Medical Science, Yonsei University College of Medicine, Seoul 03722, Korea.ORCID https://orcid.org/0000-0001-5292-1280
Jeon-Soo ShinDepartment of Microbiology, Yonsei University College of Medicine, Seoul 03722, Korea.ORCID https://orcid.org/0000-0002-8294-3234
Yonsei University · KRSeoul National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection induces excessive pro-inflammatory cytokine release and cell death, leading to organ damage and mortality. High-mobility group box 1 (HMGB1) is one of the damage-associated molecular patterns that can be secreted by pro-inflammatory stimuli, including viral infections, and its excessive secretion levels are related to a variety of inflammatory diseases. Here, the aim of the study was to show that SARS-CoV-2 infection induced HMGB1 secretion via active and passive release. Active HMGB1 secretion was mediated by post-translational modifications, such as acetylation, phosphorylation, and oxidation in HEK293E/ACE2-C-GFP and Calu-3 cells during SARS-CoV-2 infection. Passive release of HMGB1 has been linked to various types of cell death; however, we demonstrated for the first time that PANoptosis, which integrates other cell death pathways, including pyroptosis, apoptosis, and necroptosis, is related to passive HMGB1 release during SARS-CoV-2 infection. In addition, cytoplasmic translocation and extracellular secretion or release of HMGB1 were confirmed via immunohistochemistry and immunofluorescence in the lung tissues of humans and angiotensin-converting enzyme 2-overexpressing mice infected with SARS-CoV-2.

Indexed as

HMGB1 proteinPANoptosisPost-translational modificationSevere acute respiratory syndrome coronavirus 2

Identifiers

PMID37416931
PMCPMC10320423
OpenAlexW4382775544

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.