Presentation
20 June 2024 Imaging intracellular neurotransmitters with vibrational microscopy using isotopologues
Gabriel F. Dorlhiac, Bryce Manifold, Markita Landry, Aaron Streets
Author Affiliations +
Abstract
We present a new approach for imaging intracellular neurotransmitter molecules with stimulated Raman scattering microscopy. We leverage the isolated vibrational peaks of carbon-deuterium bonds to observe these neurotransmitters directly and quantitatively. By using deuterated versions of neurotransmitters, we minimize perturbation to neurochemical activity with respect to previously demonstrated fluorescence-based methods. We show direct imaging of deuterated dopamine and GABA uptake and release dynamics in PC12 chromafin cells, and in primary hippocampal neurons, respectively. Specifically, we show that stimulation of neurotransmitter release results in a 20-50% intracellular neurotransmitter concentration reduction, with the ability to observe inter- and intracellular variation in vesicular neurotransmitter release. Taken together, our data suggest that neurotransmitter isotopologues can serve as a generic, commercially-available, non-perturbative, and biocompatible method to image neurotransmitters that are chemically homologous to their native counterparts.
Conference Presentation
© (2024) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Gabriel F. Dorlhiac, Bryce Manifold, Markita Landry, and Aaron Streets "Imaging intracellular neurotransmitters with vibrational microscopy using isotopologues", Proc. SPIE PC13007, Neurophotonics II, PC1300705 (20 June 2024); https://doi.org/10.1117/12.3017344
Advertisement
Advertisement
KEYWORDS
Neurotransmitters

Microscopy

Vibration

Molecules

Neurons

Neurotransmitter release

Mental disorders

Back to Top