Félix-Antoine Pellerin

Mr. Félix-Antoine Pellerin


Research Focus & Metrics

Academic Career Length

3Years (2024-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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2 December 2024 in Journal of Xenobiotics
Verified
Journal Article
Open access
PDF file
CCChristophe Caneparo
Christophe Caneparo
LCLaurence Carignan
Laurence Carignan
ELElena Lonina
Elena Lonina
SGSarah-Maude Goulet
Sarah-Maude Goulet
FPFélix-Antoine Pellerin
Félix-Antoine Pellerin
MPMartin Pelletier
Martin Pelletier
Over the last decades, the human species has seen an increase in the incidence of pathologies linked to the genitourinary tract. Observations in animals have allowed us to link these increases, at least in part, to changes in the environment and, in particular, to an increasing presence of endocrine disruptors. These can be physical agents, such as light or heat; natural products, such as phytoestrogens; or chemicals produced by humans. Endocrine disruptors may interfere with the signaling pathways mediated by the endocrine system, particularly those linked to sex hormones. These factors and their general effects are presented before focusing on the male and female genitourinary tracts by describing their anatomy, development, and pathologies, including bladder and prostate cancer.

26 October 2024 in Microorganisms
Verified
Journal Article
Open access
PDF file
FPFélix-Antoine Pellerin
Félix-Antoine Pellerin
ÉDÉlodie Dufresne
Élodie Dufresne
Stéphane ChabaudStéphane Chabaud
Stéphane Chabaud
HOHazem Orabi
Hazem Orabi
SBStéphane Bolduc
Stéphane Bolduc
Uropathogenic Escherichia coli are the main causal agent of urinary tract infections. These diseases can affect more than half of women during their lifetime. Moreover, recurrent urinary tract infections can affect up to 30% of patients, leading to higher social and economic costs for the community. No efficient treatment against the recurrent form of the disease has been discovered. Due to the low average rate of successful translation from 2D cell culture and in vivo animal models into clinical trials, new models that mimic pathologies, such as those produced by tissue engineering, are needed. A model of human-derived 3D bladder mucosa was produced by tissue engineering techniques using collagen gels and organ-specific primary human stromal and epithelial cell populations. This model was used to mimic the different steps of a urinary tract infection: adhesion, invasion, intracellular bacterial community and quiescent intracellular reservoir formation and, finally, bacteria resurgence after umbrella cell exfoliation through chitosan exposure to mimic the recurrent infection. The uropathogenic strain UTI-89-GFP was used as infectious bacteria and BL-21-GFP strain as a control. Our model is unique and is the first step toward mimicking the different phases of a UTI in a human context.