Dr Yanfeng Zhang
Lecturer
Clinical and Biomedical Sciences
University of Exeter
Hatherly Building
Prince of Wales Roa
Exeter EX4 4PS
It is critical to learn what sensory inputs are predicting and react fast to receive a reward and avoid punishment. I am interested in understanding the cellular mechanisms underlying this learning process.
Dopamine, acetylcholine, and serotonin signals in basal ganglia are believed to play critical roles in reward-related learning. Dysfunction of these systems can lead to severe diseases, such as Parkinson’s disease. My lab explores how these neurotransmitter systems modulate connections between brain areas in basal ganglia, which remain poorly understood.
My PhD work revealed that the pauses in cholinergic interneurons may define the time window for phasic dopamine to induce plasticity, and depolarisation of SPNs constrains the plasticity to the target synapses (Reynolds, ..., Zhang†, Nature Communications, 2022). Furthermore, I investigated how the superior colliculus may regulate rapid phasic dopamine responses in visual classical conditioning (Zhang et al., under revision). Moreover, I explored how striatal cholinergic interneurons integrate top-down and bottom-up inputs in vivo (Zhang† and Reynolds, Current Neuropharmacology, 2024).
After joining Prof Stephanie Cragg's lab at Oxford University as a Postdoctoral Researcher, I characterised how cortical and thalamic inputs summate in cholinergic interneurons ex vivo with optogenetic manipulations (Kosillo, Zhang et al., 2016, Cerebral Cortex). By combining in vivo single-unit recording, whole cell patch clamp and a computational model, I revealed the multiphasic activity in cholinergic interneurons is driven by withdrawal of excitatory input through a rectifying potassium current and modulated by dopamine signal (Zhang et al., Neuron 2018). I revealed a novel mechanism by which cholinergic interneurons regulate the excitability of striatal dopamine axons, thereby influencing dopamine release in the striatum (Zhang et al., in revision). Additionally, I discovered the significant impact of tonic dopamine activity on phasic dopamine release in both health and disease states (Zhang et al., in prep). My study also led to potential treatments for Parkinson’s disease (patent application filed).
I also collaborated with E.N.T. surgeons to map sensory input from different parts of the vestibular and auditory systems stratified across the hippocampus's different subregions (Hitier*, Zhang* et al., 2020, Hearing Research; Hitier*, Zhang* et al., 2021, Hearing Research, cover story).
Qualifications:
- PhD
- PGDipSci (Distinction)
- BSc