Samantha Gruenheid
Has grant
Professor
Research Interests
Explore related searches
Contact this professor
Get a free first email built on one of their papers, ready for you to edit and send yourself.
About
Professor Samantha Gruenheid is a faculty member at McGill University in Canada. Her research focuses on microbial interactions and host-pathogen dynamics, particularly in the context of glycosylation processes and intestinal microbiota. Recent articles authored by Professor Gruenheid investigate the relationship between microbiomes and neurological conditions, as well as the mechanisms of bacterial virulence factors in host systems.
Recent Grants
Grant: Close
Defining the immune dysregulation underlying Pediatric IBD to better diagnose and treat patients.
Open Date: 2020-01-01
Close Date: 2023-12-01
Grant: Close
A new model to study the role of intestinal inflammation as a driver of Parkinson's Disease development
Open Date: 2019-04-01
Close Date: 2024-03-31
Grant: Close
Defining the immuno-dysregulation underlying Pediatric IBD to better diagnose and treat patients. (LOI stage)
Open Date: 2018-12-01
Close Date: 2019-11-30
Grant: Close
Defining the immuno-dysregulation underlying Pediatric IBD to better diagnose and treat patients.
Open Date: 2018-12-01
Close Date: 2019-11-30
Grant: Close
Exploitation du microbiome du sol arctique en vue d'identifier de nouveaux bioproduits à fort potentiel industriel
Open Date: 2017-04-01
Close Date: 2020-03-31
Articles (6)
The enteric nervous system (ENS) comprises a complex network of neurons whereby a subset appears to be dopaminergic although the characteristics, roles, and implications in disease are less understood. Most investigations relating to enteric dopamine (DA) neurons rely on immunoreactivity to tyrosine hydroxylase (TH)—the rate‐limiting enzyme in the production of DA. However, TH immunoreactivity is likely to provide an incomplete picture. This study herein provides a comprehensive characterization of DA neurons in the gut using a reporter mouse line, expressing a fluorescent protein (tdTomato) under control of the DA transporter (DAT) promoter. Our findings confirm a unique localization of DA neurons in the gut and unveil the discrete subtypes of DA neurons in this organ, which we characterized using both immunofluorescence and single‐cell transcriptomics, as well as validated using in situ hybridization. We observed distinct subtypes of DAT‐tdTomato neurons expressing co‐transmitters and modulators across both plexuses; some of them likely co‐releasing acetylcholine, while others were positive for a slew of canonical DAergic markers (TH, VMAT2 and GIRK2). Interestingly, we uncovered a seemingly novel population of DA neurons unique to the ENS which was ChAT/DAT‐tdTomato‐immunoreactive and expressed Grp , Calcb , and Sst . Given the clear heterogeneity of DAergic gut neurons, further investigation is warranted to define their functional signatures and decipher their implication in disease.
Year:
2024
Year:
2024
Year:
2023
Year:
2022
Year:
2022
Year:
2020
Collaborators (3)
Louis-Eric Trudeau
Full professor
Université de Montréal
Jo Anne Stratton
-
Mehrbod Estaki
Chief Science Officer
-
Make your next move.
Prepare your application
Review drafts before you send them.