DCBIO | In vivo functions of nuclear envelope rupture and antiviral specialization in dendritic cells

Summary
Dendritic cells (DCs) function at the interface between innate and adaptive immunity and have a crucial role in the induction of immune responses. The goal of this project is to uncover the in vivo functions of two novel molecular mechanisms that were recently identified in vitro in DCs. DCs are rapidly activated when DNA is exposed to the cytosol, which can occur in viral infections. Recent work has revealed that DNA is also transiently accessible to the cytosol in migrating DCs due to rupture of the nuclear envelope, and is detected by the cytosolic DNA sensor cGAS. In the first aim of this project we will investigate the immune consequences of nuclear envelope rupture in DCs in vivo. The second aim of this project is to investigate antiviral specialization of DC subsets. Viral infection of DCs impairs their immune functions. Unpublished data has revealed that in humans, the CD141+ DC subset is constitutively resistant to a broad range of enveloped viruses. Resistance was associated with the expression of the GTPase, RAB15. We will investigate the function of RAB15 in DC biology in vivo to study the division of antiviral labor among DC subsets.
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More information & hyperlinks
Web resources: https://cordis.europa.eu/project/id/751735
Start date: 01-02-2018
End date: 31-01-2020
Total budget - Public funding: 173 076,00 Euro - 173 076,00 Euro
Cordis data

Original description

Dendritic cells (DCs) function at the interface between innate and adaptive immunity and have a crucial role in the induction of immune responses. The goal of this project is to uncover the in vivo functions of two novel molecular mechanisms that were recently identified in vitro in DCs. DCs are rapidly activated when DNA is exposed to the cytosol, which can occur in viral infections. Recent work has revealed that DNA is also transiently accessible to the cytosol in migrating DCs due to rupture of the nuclear envelope, and is detected by the cytosolic DNA sensor cGAS. In the first aim of this project we will investigate the immune consequences of nuclear envelope rupture in DCs in vivo. The second aim of this project is to investigate antiviral specialization of DC subsets. Viral infection of DCs impairs their immune functions. Unpublished data has revealed that in humans, the CD141+ DC subset is constitutively resistant to a broad range of enveloped viruses. Resistance was associated with the expression of the GTPase, RAB15. We will investigate the function of RAB15 in DC biology in vivo to study the division of antiviral labor among DC subsets.

Status

CLOSED

Call topic

MSCA-IF-2016

Update Date

28-04-2024
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Horizon 2020
H2020-EU.1. EXCELLENT SCIENCE
H2020-EU.1.3. EXCELLENT SCIENCE - Marie Skłodowska-Curie Actions (MSCA)
H2020-EU.1.3.2. Nurturing excellence by means of cross-border and cross-sector mobility
H2020-MSCA-IF-2016
MSCA-IF-2016