Institut de Duve Avenue Hippocrate 74 - B1.75.08 1200 Bruxelles
The Veiga-da-Cunha Lab focuses on understanding the impact of specific enzyme deficiencies on intermediary metabolism to find novel treatments.
What are the dysfunctions in hexokinases that are at the origin of neutropenia and neurodevelopmental diseases? Can understanding them help to treat these disorders ?
The metabolism of glucose is essential for most cells to survive and to thrive. Yet, the need for glucose is often cell-specific, and the metabolic pathways that use glucose are differently regulated due to the existence of several versions of the enzymes catalysing the critical steps of glycolysis.
Glucose phosphorylation by hexokinases (five different enzymes) is one of these critical steps. The rate of glucose utilisation has to be adjusted to the needs for downstream metabolites (ATP, pyruvate, acetyl-CoA, serine). Accordingly, hexokinases are feed-back inhibited by glucose-6-phosphate, but in a surprising way this inhibition is not yet fully understood: it is a sophisticated feature implicating the binding of glucose-6-phosphate to an allosteric site.
With her lab, Maria Veiga-da-Cunha and Emile Van Schaftingen collaborate to understand the impact of defects in the regulation of hexokinases present in inborn errors of metabolism. These can either be due to mutations in hexokinase itself or in other enzymes (including metabolite repair enzymes) or transporters that impact the production of metabolites affecting the regulation of hexokinases.
To address these questions they use two strategies : 1) an in vitro approach, where they produce and study the enzymatic properties of the recombinant enzymes and 2) a physiological one that uses cell and mouse models that mimic the enzymatic defects that are studied by metabolic analysis.
Through understanding the pathophysiological mechanism of still enigmatic inborn errors of metabolism, the Veiga-da-Cunha lab seeks to provide new treatments for the patients.
Maria Veiga-da-Cunha obtained her degree in Bioengineering and Agricultural Sciences from the University of Lisbon (Portugal) and from UCLouvain (Belgium) in 1987. She obtained her D. Phil in 1990, in bacterial metabolism, in the department of biochemistry in the University of Oxford (United Kingdom). As a post-doctoral she first (1990 – 1992) joined the lab of Dr. Helena Santos, in the “Instituto de Tecnologia Quimica e Biológica (ITQB)” in Oeiras (Portugal) and learnt to use NMR techniques to study bacterial metabolism. In 1992, she moved to Brussels (Belgium) to join the lab of Prof. Emile Van Schaftingen in the de Duve Institute, where she began her training in inborn errors of metabolism and intermediary metabolism in eukaryotic cells. She became F.R.S-FNRS Research Associate and UCLouvain AssociateProfessor in 2000 and continued to closely collaborate with the Emile Van Schaftingen Lab until he become Emeritus in 2018. Since then, she has her lab but they continue to actively collaborate in most research projects.
Diederich J, Mounkoro P, Tirado HA, Chevalier N, Van Schaftingen E, Veiga-da-Cunha M.
Cell Mol Life Sci (2023) 80(9):259.
Boulanger C, Stephenne X, Diederich J, Mounkoro P, Chevalier N, Ferster A, Van Schaftingen E, Veiga-da-Cunha M.
J Inherit Metab Dis (2022) 45(4):759-768
Morava E, Schatz UA, Torring PM, Abbott MA, Baumann M, Brasch-Andersen C, Chevalier N, Dunkhase-Heinl U, Fleger M, Haack TB, Nelson S, Potelle S, Radenkovic S, Bommer GT, Van Schaftingen E, Veiga-da-Cunha M.
Am J Hum Genet (2021) 108:1151-1160.
Wortmann SB, Van Hove JLK, Derks TGJ, Chevalier N, Knight V, Koller A, Oussoren E, Mayr JA, van Spronsen FJ, Lagler FB, Gaughan S, Van Schaftingen E, Veiga-da-Cunha M.
Blood (2020) 136:1033-1043.
Veiga-da-Cunha M, Chevalier N, Stephenne X, Defour JP, Paczia N, Ferster A, Achouri Y, Dewulf JP, Linster CL, Bommer GT, Van Schaftingen E.
Proc Natl Acad Sci U S A. (2019) 116:1241-1250.