Author

P. Pierre

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Immunology· 3

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Research Focus:cell signaling & trafficking· 2 Organism:human· 2 Assay:proteomics· 2 Research Focus:cell type annotation· 1 Research Focus:development & morphogenesis· 1 Research Focus:drug response / drug discovery· 1 Assay:flow cytometry· 1

Frequent Co-Authors

E. Gatti· 3 shared A. Mendes· 2 shared C. Almeida· 2 shared D. Barros· 2 shared J. P. Gigan· 2 shared R. J. Argüello· 2 shared V. Camosseto· 2 shared A. J. COMBES· 1 shared

Activity by Year

2020-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 39 mutual co-author links

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3 shared papersImmunology

E. Gatti

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Author profile →

3 papers

Recent·Most cited

VPS34-IN1 inhibits cap-mediated translation and synergizes with STING to drive type-I IFN expression in human plasmacytoid DCs

P. Antas, M. Machado, F. Pinheiro, D. Barros, C. Ramalhinho, A. Mendes, B. Ferreira, D. Carvoeiro, M. Reverendo, I. F. Duarte, M. Narita, B. Su, R. J. Argüello, B. Nal Rogier, P. Pierre, , E. Gatti

VPS34-IN1 inhibits cap-mediated translation and enhances STING-driven type-I IFN expression in human plasmacytoid DCs by altering SGK3 recruitment and STING degradation.

bioRxiv · Jun 17, 2024Immunology

Developmentally regulated PERK activity renders dendritic cells insensitive to subtilase cytotoxin-induced integrated stress response

P. Pierre, A. Mendes, J. P. Gigan, C. Rodriguez Rodrigues, S. A. Choteau, D. Sanseau, D. Barros, C. Almeida, V. Camosseto, L. Chasson, A. W. Paton, J. C. Paton, R. J. Argüello, A.-M. Lennon-Dumenil, E. Gatti

The paper shows dendritic cells have high eIF2 phosphorylation due to PERK activation, but this does not lead to chronic ISR or translation arrest, allowing them to adapt to stress.

bioRxiv · Apr 27, 2020 · PreprintImmunology

SCENITH: A flow cytometry based method to functionally profile energy metabolism with single cell resolution

R. J. ARGUELLO, A. J. COMBES, R. CHAR, E. BOUSIQUOT, J. P. GIGAN, V. CAMOSSETO, B. SAMAD, J. TSUI, P. YAN, S. BOISSONNEAU, D. FIGARELLA-BRANGER, E. GATTI, E. TABOURET, M. F. Krummel, P. PIERRE

SCENITH functionally profiles energy metabolism at single-cell resolution using flow cytometry, revealing variable metabolic profiles in tumor myeloid cells not linked to lineage or activation phenotype.

bioRxiv · Mar 10, 2020Immunology