The research of Dr. Sévigny’s team focusses on the functions of extracellular nucleotides, exerted through the activation of P2 receptors, with an emphasis on the enzymes that regulate their concentrations at the cell surface. Dr. Sévigny and his team have also identified, cloned and characterized six new genes, including the first member of a new family encoding enzymes called NTPDases. His team is interested in several biological functions including the regulation of inflammation in response to pathogenic determinants, the migration of immune cells, the functions of leukocytes, the contraction of smooth muscles, and in particular the regulation of inflammation of the intestine with an emphasis on epithelial cells and on a potential treatment for inflammatory bowel disease.
Dr Sévigny’s team uses animal models with KO mice as well as methods of cell biology (murine and human primary cells), pharmacology, biochemistry and immunology.
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Assignment of ecto-nucleoside triphosphate diphosphohydrolase-1/cd39 expression to microglia and vasculature of the brain
Journal ArticleEur J Neurosci, 12 (12), 2000.
Identification, characterization, and immunolocalization of a nucleoside triphosphate diphosphohydrolase in pig liver
Journal ArticleArch Biochem Biophys, 377 (2), 2000.
Modulation of nucleoside [correction of nucleotide] triphosphate diphosphohydrolase-1 (NTPDase-1)cd39 in xenograft rejection
Journal ArticleMol Med, 5 (11), 1999.
Targeted disruption of cd39/ATP diphosphohydrolase results in disordered hemostasis and thromboregulation
Journal ArticleNat Med, 5 (9), 1999.
Analysis of CD39/ATP diphosphohydrolase (ATPDase) expression in endothelial cells, platelets and leukocytes
Journal ArticleThromb Haemost, 82 (5), 1999.
Suppression of ATP diphosphohydrolase/CD39 in human vascular endothelial cells
Journal ArticleBiochemistry, 38 (41), 1999.
Structural elements and limited proteolysis of CD39 influence ATP diphosphohydrolase activity
Journal ArticleBiochemistry, 38 (8), 1999.
CD39 as a caveolar-associated ectonucleotidase
Journal ArticleBiochem Biophys Res Commun, 262 (3), 1999.
Identification and immunolocalization of two isoforms of ATP-diphosphohydrolase (ATPDase) in the pig immune system
Journal ArticleArch Biochem Biophys, 370 (2), 1999.
Prevention and reversal of thrombotic and inflammatory processes
Journal ArticleEmerging therapeutic targets, 2 (1), 1998.
Active projects
- A recombinant soluble NTPDase8 as a novel biological treatment for inflammatory bowel disease, from 2021-10-01 to 2026-09-30
- Ectonucleotidases and Extracellular Nucleotides in Smooth Muscle Cell Contraction, from 2023-04-01 to 2028-03-31
- Novel P2Y6 antagonists as a potential therapy for inflammatory bowel disease, from 2021-07-01 to 2025-06-30
- Scaling up the production of recombinant human NTPDase8 in CHO expression system for in vivo testing, from 2023-09-01 to 2024-03-31
Recently finished projects
- A novel approach to treating inflammatory bowel diseases through the blocking of P2Y6 receptors, from 2018-04-01 to 2023-03-31
- Role of NTPDase1 and Extracellular Nucleotides in Smooth Muscle Cell Contraction., from 2016-04-01 to 2022-03-31