Dr. Paul Isenring has been a Professor of Medicine in the Department of Medicine at Laval University since 2011. He holds a doctorate in medicine, which he obtained in 1986 from Laval University, as well as certificates in internal medicine and nephrology, obtained in 1989 and 1991 from the Collège des médecins du Québec and the Royal College of Physicians and Surgeons of Canada. Upon completing his training in Nephrology, he began graduate studies at Yale University, where he obtained a PhD in molecular physiology in early 1996. He then pursued postdoctoral studies for three years at the same institution before establishing himself as an independent researcher at L’Hôtel-Dieu de Québec’s Research Centre.
Since returning to Quebec, Dr. Isenring has devoted 70% of his time to research, working mainly in the field of applied membrane transport. He is particularly interested in a family of membrane proteins called cation-chloride cotransporters, whose role is to allow the passage of chloride with that of sodium and/or potassium across the cell surface. He is more specifically interested in the molecular determinants that underlie the function, assembly and regulation of these proteins, as well as their roles in the renal tubular epithelium and the cardiovascular system. To achieve his goals, he made use of different heterologous expression systems and animal models, while using directed mutagenesis.
Dr. Isenring has three other fields of interest. He is working to discover new transport systems by characterizing the function of candidate proteins whose role is either unknown or more complex than demonstrated in previous studies. He is also involved in the investigation of various human genetic diseases through the identification of associated mutations as well as in vitro characterization of genetic defects. Finally, Dr. Isenring devotes a part of his time to the care of patients who are suffering from electrolyte disorders and nephrological problems, while also teaching externs and residents of medicine.
The work of Dr. Isenring and his team has led to several discoveries such as the identification of (1) several mechanisms that allow cation-chloride cotransporters to perform both their operational and physiological roles, and to be regulated at the plasma membrane, (2) new functions for different membrane proteins , including that of silicon transport by aquaporins, and (3) unprecedented nosological entities or pathogenic mechanisms hitherto unknown.
10, rue McMahon
3853-1
Québec, Québec
Canada G1R 2J6
- Bergeron, NicolasInternnicolas.bergeron@crchudequebec.ulaval.ca
- Fiola, Marie-JeanneEmployeeL'Hôtel-Dieu de Québec+1 418-525-4444, extension 16867+1 418-654-2715marie-jeanne.fiola@crchudequebec.ulaval.ca
9 Rue Mcmahon
3852
Québec, QC
Canada G1R 3S3 - Garneau, AlexandreDoctoral studentL'Hôtel-Dieu de Québec+1 418-525-4444, extension 16866+1 418-691-5562alexandre.garneau.2@umontreal.caalexandre.garneau@crchudequebec.ulaval.ca
10, rue McMahon
3852
Québec, Québec
Canada G1R 2J6 - Gravel, MathieuInternL'Hôtel-Dieu de Québecmathieu.gravel@crchudequebec.ulaval.ca
10 rue McMahon
Québec, QC
Canada G1R 3S1 - Hammache, MeriemInternL'Hôtel-Dieu de Québec+1 418-525-4444, extension 16867meriem.hammache.1@ulaval.ca
10 rue McMahon
3852
Québec, QC
Canada G1R 3S1 - Nsimba, Thy-René BatomeneDoctoral studentL'Hôtel-Dieu de Québec
10 rue McMahon
3852
Québec, QC
Canada G1R 3S1L'Hôtel-Dieu de Québec+1 418-525-4444, extension 16866+1 418-525-4444, extension 16867thy-rene.nsimba-batomene@crchudequebec.ulaval.ca
10 rue McMahon
3880
Québec, QC
Canada G1R 3S1 - Slimani, SamiraDoctoral studentL'Hôtel-Dieu de Québec+1 418-525-4444, extension 16866+1 418-691-5562samira.slimani.1@ulaval.casamira.slimani@crchudequebec.ulaval.ca
10, rue McMahon
3852
Québec, Québec
Canada G1R 3S1
Homooligomeric and heterooligomeric associations between K+-Cl- cotransporter isoforms and between K+-Cl- and Na+-K+-Cl- cotransporters
Journal ArticleJ Biol Chem, 282 (25), 2007.
Hypercalcaemia in a patient with membraneous nephropathy
Journal ArticleNephrol Dial Transplant, 21 (5), 2006.
Identification of key functional domains in the C terminus of the K+-Cl- cotransporters
Journal ArticleJ Biol Chem, 281 (23), 2006.
Novel insights regarding the operational characteristics and teleological purpose of the renal Na+-K+-Cl2 cotransporter (NKCC2s) splice variants
Journal ArticleJ Gen Physiol, 126 (4), 2005.
Molecular mechanisms of cation transport by the renal Na+-K+-Cl- cotransporter: structural insight into the operating characteristics of the ion transport sites
Journal ArticleJ Biol Chem, 280 (37), 2005.
Changes in gene expression in gills of the euryhaline killifish Fundulus heteroclitus after abrupt salinity transfer
Journal ArticleAm J Physiol Cell Physiol, 287 (2), 2004.
Molecular mechanisms of Cl- transport by the renal Na(+)-K(+)-Cl- cotransporter. Identification of an intracellular locus that may form part of a high affinity Cl(-)-binding site
Journal ArticleJ Biol Chem, 279 (7), 2004.
Self-interacting domains in the C terminus of a cation-Cl- cotransporter described for the first time
Journal ArticleJ Biol Chem, 279 (39), 2004.
Characterization of a novel interaction between the secretory Na+-K+-Cl- cotransporter and the chaperone hsp90
Journal ArticleJ Biol Chem, 279 (46), 2004.
Ammonium transport and pH regulation by K(+)-Cl(-) cotransporters
Journal ArticleAm J Physiol Renal Physiol, 285 (1), 2003.
Active projects
- Molecular characterization of newly identified silicon transporters in animals, from 2021-04-01 to 2026-03-31
- Suivis de la thérapeutique d'une maladie rare et de la modification du facteur de risque cardiovasculaire , from 2019-08-09 to 2025-12-25
Recently finished projects
- Molecular characterization of renal K-Cl cotransporters, from 2020-10-01 to 2022-09-30
- Molecular characterization of the Na-K-Cl cotransporter 2 (NKCC2) splice variants in the thick ascending loop of Henle, from 2022-03-01 to 2023-02-28
- Nouveau paradigme du transport de silicium chez les plantes dans un contexte d’une agriculture durable, from 2020-04-01 to 2023-03-31
- Projet de recherche clinique visant à identifier le gène responsable de la lipomatose chez un patient. , from 2021-12-22 to 2022-03-31