Max Rady College of Medicine
Physiology and Pathophysiology
Room 429 – 745 Bannatyne Avenue
University of Manitoba
Winnipeg, Manitoba R3E 0J9
Phone: 204-789-3524
Fax: 204-789-3934
robin.dasilva@umanitoba.ca
The University of Manitoba campuses are located on original lands of Anishinaabeg, Ininew, Anisininew, Dakota and Dene peoples, and on the National Homeland of the Red River Métis. More
University of Manitoba
Winnipeg, Manitoba Canada, R3T 2N2
Max Rady College of Medicine
Physiology and Pathophysiology
Room 429 – 745 Bannatyne Avenue
University of Manitoba
Winnipeg, Manitoba R3E 0J9
Phone: 204-789-3524
Fax: 204-789-3934
robin.dasilva@umanitoba.ca
The da Silva lab studies metabolism and the role of metabolites as signaling molecules that regulate the function of immune cells. We mainly focus on the folate and B12 dependent amino acid and nucleotide metabolic pathways.
One of our main interests is furthering our understanding of the molecular mechanisms of fibrosis in liver disease. Non-alcoholic fatty liver disease (NAFLD) and metabolic dysfunction-associated steatotic liver disease (MASLD) are prevalent conditions in developed countries affecting approximately 35% of the population. Liver diseases progress to serious fibrotic liver disease for which there are no effective treatments. Fibrosis is the primary predictor of organ failure. We believe that a better understanding of the crosstalk between metabolism and immune signaling are key to the discovery of novel therapies for this condition.
Tryptophan: Stellate cells are key immune cells in the liver that can differentiate into myofibroblasts and cause fibrosis. We are currently investigating the role of endogenous and gut microbial tryptophan metabolites in the activation of hepatic stellate cells through the aryl hydrocarbon receptor in liver fibrosis.
Adenosine: Adenosine receptors are G-protein coupled receptors that regulate immune cell function. The role of adenosine receptors is not clear in the literature and the regulation of cellular adenosine production is unknown. We have discovered that augmenting the metabolism of methionine can influence adenosine signaling in macrophages that regulates phagocytosis.
Dr. da Silva hails from St. John’s Newfoundland and is now an assistant professor in physiology and pathophysiology in the Rady faculty of Health Sciences at the University of Manitoba.
Dr. da Silva obtained his initial training in biochemistry and amino acid metabolism at Memorial University of Newfoundland with a focus on creatine biosynthesis and non-alcoholic fatty liver disease. He then worked as a post-doctoral researcher studying lipid metabolism as a part of the Molecular and Cell Biology of Lipids group at the University of Alberta.
Prior to Manitoba Dr. da Silva was an assistant professor in food science and human nutrition at the University of Florida developing studies on the functions of Adenosine receptors in immune cells.
Dr. da Silva has developed several successful collaborations including work with the Center for Disease Control and Prevention (CDC) studying interactions of HIV treatments on vitamin B3 (niacin) status and Pellagra in Malawi.
Physiology and Pathophysiology
432 Basic Medical Sciences Building
745 Bannatyne Avenue
University of Manitoba
Winnipeg, MB R3E 0J9 Canada