Evidence map›Paper›PMID 32199615›Full record

ArticleBiochemical and biophysical research communications2020

Single cell RNA sequencing of 13 human tissues identify cell types and receptors of human coronaviruses.

Furong Qi, Shen Qian, Shuye Zhang, Zheng Zhang

Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in Biochemical and biophysical research communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04362059 (A Clinical Trial of Nebulized Surfactant for the Treatment of Moderate to Severe COVID-19), which is not on this map. Cited by 589 papers, 7 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
589citing papers in PubMed, 7 pooled it
67.9field-weighted citation impact, top 1% 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.

NCT04362059 nacompletednot on this map

A Clinical Trial of Nebulized Surfactant for the Treatment of Moderate to Severe COVID-19

TypeinterventionalSponsorUniversity Hospital Southampton NHS Foundation TrustRan2020 to 2023Enrolled20ConditionsRespiratory InfectionsArmsCOVSurf Drug Delivery System, Standard of Care
3 · Its place in the literature

Who cites it

589 citing papers in PubMed, 7 syntheses or guidelines pooled it, 908 citations in OpenAlex.

  1. Pooled it
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  5. Gut distress and interventionFrontiers in public health · 2023
    Pooled it
  6. SARS-CoV-2 cell entry beyond the ACE2 receptor.Molecular biology reports · 2022
    Pooled it
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529 more citing papers are in PubMed but not listed here.

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

4 authors at 3 institutions in 1 country.

Furong QiInstitute of Hepatology, National Clinical Research Center for Infectious Disease, Shenzhen Third People's Hospital, Shenzhen, Guangdong Province, 518100, China.
Shen QianInstitute of Hepatology, National Clinical Research Center for Infectious Disease, Shenzhen Third People's Hospital, Shenzhen, Guangdong Province, 518100, China.
Shuye ZhangShanghai Public Health Clinical Center and Institute of Biomedical Sciences, Fudan University, Shanghai, China. Electronic address: zhangshuye@shphc.org.cn.
Zheng ZhangInstitute of Hepatology, National Clinical Research Center for Infectious Disease, Shenzhen Third People's Hospital, Shenzhen, Guangdong Province, 518100, China; The Second Affiliated Hospital of Southern University of Science and Technology, Shenzhen, Guangdong Province, 518112, China. Electronic address: zhangzheng1975@aliyun.com.
Shenzhen Third People’s Hospital · CNShanghai Public Health Clinical Center · CNSouthern University of Science and Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The new coronavirus (SARS-CoV-2) outbreak from December 2019 in Wuhan, Hubei, China, has been declared a global public health emergency. Angiotensin I converting enzyme 2 (ACE2), is the host receptor by SARS-CoV-2 to infect human cells. Although ACE2 is reported to be expressed in lung, liver, stomach, ileum, kidney and colon, its expressing levels are rather low, especially in the lung. SARS-CoV-2 may use co-receptors/auxiliary proteins as ACE2 partner to facilitate the virus entry. To identify the potential candidates, we explored the single cell gene expression atlas including 119 cell types of 13 human tissues and analyzed the single cell co-expression spectrum of 51 reported RNA virus receptors and 400 other membrane proteins. Consistent with other recent reports, we confirmed that ACE2 was mainly expressed in lung AT2, liver cholangiocyte, colon colonocytes, esophagus keratinocytes, ileum ECs, rectum ECs, stomach epithelial cells, and kidney proximal tubules. Intriguingly, we found that the candidate co-receptors, manifesting the most similar expression patterns with ACE2 across 13 human tissues, are all peptidases, including ANPEP, DPP4 and ENPEP. Among them, ANPEP and DPP4 are the known receptors for human CoVs, suggesting ENPEP as another potential receptor for human CoVs. We also conducted "CellPhoneDB" analysis to understand the cell crosstalk between CoV-targets and their surrounding cells across different tissues. We found that macrophages frequently communicate with the CoVs targets through chemokine and phagocytosis signaling, highlighting the importance of tissue macrophages in immune defense and immune pathogenesis.

Indexed as

Sequence Analysis, RNASingle-Cell AnalysisAngiotensin-Converting Enzyme 2BetacoronavirusCoronavirusCoronavirus InfectionsCOVID-19HumansMacrophagesOrgan SpecificityPandemicsPeptide HydrolasesPeptidyl-Dipeptidase APneumonia, ViralReceptors, VirusSARS-CoV-2ACE2 protein, humanAngiotensin-Converting Enzyme 2Peptide HydrolasesPeptidyl-Dipeptidase AReceptors, VirusACE2Co-receptorCoronavirusesMacrophageSARS-CoV-2scRNA-seq

Identifiers

PMID32199615
PMCPMC7156119
OpenAlexW3011994656

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.