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SARS-CoV-2 receptor ACE2 and TMPRSS2 are primarily expressed in bronchial transient secretory cells.

Identifieur interne : 000264 ( Main/Exploration ); précédent : 000263; suivant : 000265

SARS-CoV-2 receptor ACE2 and TMPRSS2 are primarily expressed in bronchial transient secretory cells.

Auteurs : Soeren Lukassen [Allemagne] ; Robert Lorenz Chua [Allemagne] ; Timo Trefzer [Allemagne] ; Nicolas C. Kahn [Allemagne] ; Marc A. Schneider [Allemagne] ; Thomas Muley [Allemagne] ; Hauke Winter [Allemagne] ; Michael Meister [Allemagne] ; Carmen Veith [Allemagne] ; Agnes W. Boots [Pays-Bas] ; Bianca P. Hennig [Allemagne] ; Michael Kreuter [Allemagne] ; Christian Conrad [Allemagne] ; Roland Eils [Allemagne]

Source :

RBID : pubmed:32246845

Abstract

The SARS-CoV-2 pandemic affecting the human respiratory system severely challenges public health and urgently demands for increasing our understanding of COVID-19 pathogenesis, especially host factors facilitating virus infection and replication. SARS-CoV-2 was reported to enter cells via binding to ACE2, followed by its priming by TMPRSS2. Here, we investigate ACE2 and TMPRSS2 expression levels and their distribution across cell types in lung tissue (twelve donors, 39,778 cells) and in cells derived from subsegmental bronchial branches (four donors, 17,521 cells) by single nuclei and single cell RNA sequencing, respectively. While TMPRSS2 is strongly expressed in both tissues, in the subsegmental bronchial branches ACE2 is predominantly expressed in a transient secretory cell type. Interestingly, these transiently differentiating cells show an enrichment for pathways related to RHO GTPase function and viral processes suggesting increased vulnerability for SARS-CoV-2 infection. Our data provide a rich resource for future investigations of COVID-19 infection and pathogenesis.

DOI: 10.15252/embj.20105114
PubMed: 32246845


Affiliations:


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Le document en format XML

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<div type="abstract" xml:lang="en">The SARS-CoV-2 pandemic affecting the human respiratory system severely challenges public health and urgently demands for increasing our understanding of COVID-19 pathogenesis, especially host factors facilitating virus infection and replication. SARS-CoV-2 was reported to enter cells via binding to ACE2, followed by its priming by TMPRSS2. Here, we investigate ACE2 and TMPRSS2 expression levels and their distribution across cell types in lung tissue (twelve donors, 39,778 cells) and in cells derived from subsegmental bronchial branches (four donors, 17,521 cells) by single nuclei and single cell RNA sequencing, respectively. While TMPRSS2 is strongly expressed in both tissues, in the subsegmental bronchial branches ACE2 is predominantly expressed in a transient secretory cell type. Interestingly, these transiently differentiating cells show an enrichment for pathways related to RHO GTPase function and viral processes suggesting increased vulnerability for SARS-CoV-2 infection. Our data provide a rich resource for future investigations of COVID-19 infection and pathogenesis.</div>
</front>
</TEI>
<affiliations>
<list>
<country>
<li>Allemagne</li>
<li>Pays-Bas</li>
</country>
<region>
<li>Bade-Wurtemberg</li>
<li>Berlin</li>
<li>District de Karlsruhe</li>
</region>
<settlement>
<li>Berlin</li>
<li>Heidelberg</li>
</settlement>
</list>
<tree>
<country name="Allemagne">
<region name="Berlin">
<name sortKey="Lukassen, Soeren" sort="Lukassen, Soeren" uniqKey="Lukassen S" first="Soeren" last="Lukassen">Soeren Lukassen</name>
</region>
<name sortKey="Chua, Robert Lorenz" sort="Chua, Robert Lorenz" uniqKey="Chua R" first="Robert Lorenz" last="Chua">Robert Lorenz Chua</name>
<name sortKey="Conrad, Christian" sort="Conrad, Christian" uniqKey="Conrad C" first="Christian" last="Conrad">Christian Conrad</name>
<name sortKey="Eils, Roland" sort="Eils, Roland" uniqKey="Eils R" first="Roland" last="Eils">Roland Eils</name>
<name sortKey="Hennig, Bianca P" sort="Hennig, Bianca P" uniqKey="Hennig B" first="Bianca P" last="Hennig">Bianca P. Hennig</name>
<name sortKey="Kahn, Nicolas C" sort="Kahn, Nicolas C" uniqKey="Kahn N" first="Nicolas C" last="Kahn">Nicolas C. Kahn</name>
<name sortKey="Kreuter, Michael" sort="Kreuter, Michael" uniqKey="Kreuter M" first="Michael" last="Kreuter">Michael Kreuter</name>
<name sortKey="Meister, Michael" sort="Meister, Michael" uniqKey="Meister M" first="Michael" last="Meister">Michael Meister</name>
<name sortKey="Muley, Thomas" sort="Muley, Thomas" uniqKey="Muley T" first="Thomas" last="Muley">Thomas Muley</name>
<name sortKey="Schneider, Marc A" sort="Schneider, Marc A" uniqKey="Schneider M" first="Marc A" last="Schneider">Marc A. Schneider</name>
<name sortKey="Trefzer, Timo" sort="Trefzer, Timo" uniqKey="Trefzer T" first="Timo" last="Trefzer">Timo Trefzer</name>
<name sortKey="Veith, Carmen" sort="Veith, Carmen" uniqKey="Veith C" first="Carmen" last="Veith">Carmen Veith</name>
<name sortKey="Winter, Hauke" sort="Winter, Hauke" uniqKey="Winter H" first="Hauke" last="Winter">Hauke Winter</name>
</country>
<country name="Pays-Bas">
<noRegion>
<name sortKey="Boots, Agnes W" sort="Boots, Agnes W" uniqKey="Boots A" first="Agnes W" last="Boots">Agnes W. Boots</name>
</noRegion>
</country>
</tree>
</affiliations>
</record>

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