Evidence map›Paper›PMID 33922476›Full record

ArticlePathogens (Basel, Switzerland)2021

Cell-Type Apoptosis in Lung during SARS-CoV-2 Infection.

Yakun Liu, Tania M Garron, Qing Chang, Zhengchen Su, Changcheng Zhou, Yuan Qiu, Eric C Gong, Junying Zheng, Y Whitney Yin, Thomas Ksiazek and 5 more

Open access · goldAbstract read
In one paragraph

Article in Pathogens (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.5field-weighted citation impact, top 6% 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

29 citing papers in PubMed, 58 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Article
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  6. Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. iScience · 2023
    Review
  12. Review
  13. Article
  14. Role of the extracellular matrix in COVID-19.World journal of clinical cases · 2023
    Review
  15. Review
  16. Contribution to pathogenesis of accessory proteins of deadly human coronaviruses.Frontiers in cellular and infection microbiology · 2023
    Review
  17. Host mitochondria: more than an organelle in SARS-CoV-2 infection.Frontiers in cellular and infection microbiology · 2023
    Review
  18. Article
  19. Review
  20. COVID-19 disease and immune dysregulation.Best practice & research. Clinical haematology · 2022
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 2 institutions in 1 country.

Yakun LiuDepartment of Pathology, University of Texas Medical Branch, Galveston, TX 77555, USA.
Tania M GarronDepartment of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX 77555, USA.
Qing ChangDepartment of Pathology, University of Texas Medical Branch, Galveston, TX 77555, USA.
Zhengchen SuDepartment of Pathology, University of Texas Medical Branch, Galveston, TX 77555, USA.
Changcheng ZhouDepartment of Pathology, University of Texas Medical Branch, Galveston, TX 77555, USA.
Yuan QiuDepartment of Pathology, University of Texas Medical Branch, Galveston, TX 77555, USA.
Eric C GongDepartment of Pathology, University of Texas Medical Branch, Galveston, TX 77555, USA.
Junying ZhengDepartment of Neuroscience and Cell Biology, University of Texas Medical Branch, Galveston, TX 77555, USA.
Y Whitney YinDepartment of Biochemistry and Molecular Biology, University of Texas Medical Branch, Galveston, TX 77555, USA.ORCID 0000-0001-7063-9385
Thomas KsiazekDepartment of Pathology, University of Texas Medical Branch, Galveston, TX 77555, USA.
Trevor BraselDepartment of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX 77555, USA.
Yang JinDivision of Pulmonary and Critical Care Medicine, Department of Medicine, Boston University Medical Campus, Boston, MA 02118, USA.
Paul BoorDepartment of Pathology, University of Texas Medical Branch, Galveston, TX 77555, USA.
Jason E ComerDepartment of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX 77555, USA.
Bin GongDepartment of Pathology, University of Texas Medical Branch, Galveston, TX 77555, USA.
The University of Texas Medical Branch at Galveston · USBoston University · US

Funding

LncRNA regulates lung inflammationR01HL142758 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI JIN, YANG · 2019 to 2022
$2.0M
Epac1 Plays a Critical Role in Bacterial Adhesion during RickettsiosesR01AI121012 · NIAID · UNIVERSITY OF TEXAS MED BR GALVESTON · PI GONG, BIN · 2016 to 2020
$1.9M
Development of the RNA molecule-enriched, cell type-specific exosomesR33AI121644 · NIAID · BOSTON UNIVERSITY MEDICAL CAMPUS · PI JIN, YANG · 2018 to 2020
$1.4M
Mechanistic insights of inflammation and organ failure after trauma or critical illnessR01GM127596 · NIGMS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI JIN, YANG · 2018 to 2021
$1.3M
Targeting the Host Adenosine A2A Receptor to Protect Against Fatal Rickettsiosis Using an Approved Parkinson's Disease DrugR21AI137785 · NIAID · UNIVERSITY OF TEXAS MED BR GALVESTON · PI GONG, BIN · 2018 to 2019
$440k
The role of IL-1 family of cytokines in tick-transmitted ehrlichiosisR21AI144328 · NIAID · UNIVERSITY OF TEXAS MED BR GALVESTON · PI GONG, BIN · 2019 to 2020
$435k
Targeting extracellular tRNA-derived RNA fragments (tRFs) to protect against fatal rickettsiosisR21AI154211 · NIAID · UNIVERSITY OF TEXAS MED BR GALVESTON · PI GONG, BIN · 2020 to 2021
$435k
Inflammasome activation and ehrlichial dissemination in tick vs needle transmissionR03AI142406 · NIAID · UNIVERSITY OF TEXAS MED BR GALVESTON · PI GONG, BIN · 2019 to 2020
$158k
Division of Microbiology and Infectious Diseases, National Institute of Allergy and Infectious Diseases R01AI121012Division of Microbiology and Infectious Diseases, National Institute of Allergy and Infectious Diseases R03AI142406Division of Microbiology and Infectious Diseases, National Institute of Allergy and Infectious Diseases R21AI137785Division of Microbiology and Infectious Diseases, National Institute of Allergy and Infectious Diseases R21AI154211NHLBI NIH HHS R01 HL142758NIAID NIH HHS R01 AI121012NIAID NIH HHS R03 AI142406NIAID NIH HHS R21 AI137785NIAID NIH HHS R21 AI144328NIAID NIH HHS R21 AI154211NIAID NIH HHS R33 AI121644NIGMS NIH HHS R01 GM127596
6 · The paper itself

Abstract

The SARS-CoV-2 pandemic has inspired renewed interest in understanding the fundamental pathology of acute respiratory distress syndrome (ARDS) following infection. However, the pathogenesis of ARDS following SRAS-CoV-2 infection remains largely unknown. In the present study, we examined apoptosis in postmortem lung sections from COVID-19 patients and in lung tissues from a non-human primate model of SARS-CoV-2 infection, in a cell-type manner, including type 1 and 2 alveolar cells and vascular endothelial cells (ECs), macrophages, and T cells. Multiple-target immunofluorescence assays and Western blotting suggest both intrinsic and extrinsic apoptotic pathways are activated during SARS-CoV-2 infection. Furthermore, we observed that SARS-CoV-2 fails to induce apoptosis in human bronchial epithelial cells (i.e., BEAS2B cells) and primary human umbilical vein endothelial cells (HUVECs), which are refractory to SARS-CoV-2 infection. However, infection of co-cultured Vero cells and HUVECs or Vero cells and BEAS2B cells with SARS-CoV-2 induced apoptosis in both Vero cells and HUVECs/BEAS2B cells but did not alter the permissiveness of HUVECs or BEAS2B cells to the virus. Post-exposure treatment of the co-culture of Vero cells and HUVECs with a novel non-cyclic nucleotide small molecule EPAC1-specific activator reduced apoptosis in HUVECs. These findings may help to delineate a novel insight into the pathogenesis of ARDS following SARS-CoV-2 infection.

Indexed as

apoptosisco-cultureendothelial cellepithelial cellhumanlungnon-human primateSARS-CoV-2TUNEL assay

Identifiers

PMID33922476
PMCPMC8145065
OpenAlexW3158998799

What OpenQuestion holds

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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.