Abstract

Abstract It has been known that, the novel coronavirus, 2019-nCoV, which is considered similar to SARS-CoV, invades human cells via the receptor angiotensin converting enzyme II (ACE2). Moreover, lung cells that have ACE2 expression may be the main target cells during 2019-nCoV infection. However, some patients also exhibit non-respiratory symptoms, such as kidney failure, implying that 2019-nCoV could also invade other organs. To construct a risk map of different human organs, we analyzed the single-cell RNA sequencing (scRNA-seq) datasets derived from major human physiological systems, including the respiratory, cardiovascular, digestive, and urinary systems. Through scRNA-seq data analyses, we identified the organs at risk, such as lung, heart, esophagus, kidney, bladder, and ileum, and located specific cell types (i.e., type II alveolar cells (AT2), myocardial cells, proximal tubule cells of the kidney, ileum and esophagus epithelial cells, and bladder urothelial cells), which are vulnerable to 2019-nCoV infection. Based on the findings, we constructed a risk map indicating the vulnerability of different organs to 2019-nCoV infection. This study may provide potential clues for further investigation of the pathogenesis and route of 2019-nCoV infection.

Keywords

BiologyLungKidneyCellReceptorSingle-cell analysisCell typeCoronavirusImmunologyCoronavirus disease 2019 (COVID-19)PathologyMedicineInternal medicineEndocrinologyDiseaseGenetics

MeSH Terms

Angiotensin-Converting Enzyme 2BetacoronavirusCOVID-19Coronavirus InfectionsHumansOrgan SpecificityPandemicsPeptidyl-Dipeptidase APneumoniaViralRNA-SeqRisk FactorsSARS-CoV-2Single-Cell Analysis

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Publication Info

Year
2020
Type
article
Volume
14
Issue
2
Pages
185-192
Citations
2355
Access
Closed

Citation Metrics

2355
OpenAlex
80
Influential

Cite This

Xin Zou, Ke Chen, Jiawei Zou et al. (2020). Single-cell RNA-seq data analysis on the receptor ACE2 expression reveals the potential risk of different human organs vulnerable to 2019-nCoV infection. Frontiers of Medicine , 14 (2) , 185-192. https://doi.org/10.1007/s11684-020-0754-0

Identifiers

DOI
10.1007/s11684-020-0754-0
PMID
32170560
PMCID
PMC7088738

Data Quality

Data completeness: 86%