Glia and gut neuroinflammation
Enteric glial cells sense inflammation and misfolded proteins in the gut wall. We study how they respond to rotenone, LPS and α-synuclein, and whether they help spread or contain pathology.
Decoding Neural Systems
We build human gut–brain models on a chip to follow how α-synuclein travels from the intestine to neurons, and what enteric glia do along the way. The aim is to find early biomarkers and drug targets, years before motor symptoms appear.
Parkinson’s disease may start in the enteric nervous system long before the brain is affected. We combine organ-on-chip biology, glial cell biology and computational pharmacology to study that early window.
Enteric glial cells sense inflammation and misfolded proteins in the gut wall. We study how they respond to rotenone, LPS and α-synuclein, and whether they help spread or contain pathology.
We build human microfluidic models that connect the gut and the nervous system, so we can follow how α-synuclein and inflammatory signals move between them under controlled conditions.
We test whether approved drugs can calm glial inflammation, and use network pharmacology, molecular docking and explainable machine learning to pick targets and read biomarker patterns.
Principal Investigator · Associate Professor of Medical Pharmacology
Dilara Nemutlu Samur is an Associate Professor of Medical Pharmacology at Alanya Alaaddin Keykubat University, Türkiye. She trained as a pharmacist and received her PhD in Medical Pharmacology. She investigates how enteric glial cells contribute to the earliest, prodromal stage of body-first Parkinson’s disease, focusing on the neuroimmune signalling and autophagy-lysosomal pathways through which these cells handle alpha-synuclein, in cellular, rodent and microfluidic gut–brain axis models. She has been a visiting researcher at the University of Manchester and the University of Oxford. A recipient of the 2025 L’Oréal–UNESCO For Women in Science Türkiye award, she is developing microfluidic and organ-on-chip approaches to model gut–brain communication. Her research integrates established experimental models with human-relevant cellular platforms and computational methods to investigate disease mechanisms, non-motor manifestations, and potential therapeutic targets.
Our work is supported by national and international funders and carried out with collaborators in Türkiye and abroad.
Modelling the gut–brain axis in early Parkinson’s disease: α-synuclein transport on a microfluidic chip and machine-learning analysis of glial responses.
Gut–brain axis-on-a-chip to identify glia-conditioned structural signatures of α-synuclein in early Parkinson’s disease. Proposed with the University of Twente.
Health Institutes of Türkiye. Oridonin, TLR4 signalling and autophagy in Parkinson’s disease from a gut–brain axis perspective.
Two projects on vortioxetine and TLR2/S100B signalling in the brain and enteric nervous system of rotenone-treated rats.
Institutional projects on enteric glia, neuroinflammation and Parkinson’s disease models.
Microfluidic Neurological Models Lab, Radcliffe Department of Medicine.
Editorial work, talks and interviews.
“Body–Brain Interactions in Parkinson’s Disease: Experimental Models and Emerging Technologies.” Submissions on experimental models and new technologies are welcome.
A conversation with BinYaprak about gut-first Parkinson’s research (in Turkish). Read the interview
Dilara talks about the gut–brain axis and early Parkinson’s disease (in Turkish). Watch on YouTube
Selected papers. The full list is on ORCID and Google Scholar.
We are looking for curious people who like both the bench and the keyboard. Training in cell culture, microfluidics and computational methods is part of the job.
Send a short CV and a paragraph on what you would like to work on.
Questions about our research, collaborations and open positions are welcome.
dilaranemutlu [at] gmail.com