Nicola Pordone

ORCID: 0000-0003-2702-4945
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About
Contact & Profiles
Research Areas
  • Hippo pathway signaling and YAP/TAZ
  • Autophagy in Disease and Therapy
  • CRISPR and Genetic Engineering
  • Cellular transport and secretion

Université Jean Monnet
2022-2023

Centre International de Recherche en Infectiologie
2022-2023

Inserm
2022-2023

Université Claude Bernard Lyon 1
2022-2023

École Normale Supérieure de Lyon
2022-2023

Centre National de la Recherche Scientifique
2022-2023

Abstract Transcriptional cofactors YAP/TAZ have recently been found to support autophagy and inflammation, which are part of cell-autonomous immunity critical in antibacterial defense. Here, we studied the role YAP against Staphylococcus aureus using CRISPR/Cas9-mutated HEK293 cells a primary cell-based organoid model. We that S. infection increases transcriptional activity, is required reduce intracellular replication. A 770-gene targeted transcriptomic analysis revealed upregulates genes...

10.1038/s41467-022-34432-0 article EN cc-by Nature Communications 2022-11-16

Previously considered as an exclusive extracellular bacterium, Staphylococcus aureus has been shown to be able invade many cells in vitro and humans. Once inside the host cell, both cytosolic endosome-associated S. strongly induce macroautophagy/autophagy. Whether autophagy fosters intracellular survival or clearance remains unclear. The YAP1-TEAD axis regulates expression of target genes controlling cell fate (e.g., proliferation, migration, cycle …). Growing evidence indicates that also...

10.1080/15548627.2023.2179771 article EN Autophagy 2023-02-13
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