During the past decade, emerging studies using electrochemistry and nanoscale imaging have demonstrated that partial exocytotic release is prevailing in neuroendocrine cell models. However, due to complicated structure and culture process, few studies have been carried out using neurons, especially human neurons. Here, dopamine (DA) release from individual vesicles and DA content stored within vesicles were quantified from induced pluripotent stem cell-derived DA neurons with electrochemical techniques. The results indicate that around 61% of the total vesicular DA content is released from these neurons during exocytosis. The vesicular content quantified in DA neurons is significantly higher than that in undifferentiated neural progenitor cells, owing to the increased appearance of dense-core vesicles that are able to store more DA molecules than the clear vesicles. When the neurons are differentiated with BAY-K8644, which stimulates neuronal maturation as well as DA release, the release fraction rises to 91%. The use of BAY-K8644 can be considered as chronic stimulation and leads to similar effects on exocytosis as repetitive stimulation, which triggers short-term plasticity. This study demonstrates partial release in DA transmission in human neurons and provides a link between neuronal maturation and the formation of plasticity. Furthermore, this work suggests that the fraction of release in exocytosis at human neurons may be a factor in determining plasticity.

Infrared (IR) nanoscopy represents a collection of imaging and spectroscopy techniques capable of resolving IR absorption on the nanometer scale. Chemical specificity is leveraged from vibrational spectroscopy, while light–matter interactions are detected by observing perturbations in the optical near field with an atomic force microscopy probe. Therefore, imaging is wavelength independent and has a spatial resolution on the nanometer scale, well beyond the classical diffraction limit. In this perspective, we outline the recent biological applications of scattering type scanning near-field optical microscopy and nanoscale Fourier-transform IR spectroscopy. These techniques are uniquely suited to resolving subcellular ultrastructure from a variety of cell types, as well as studying biological processes such as metabolic activity on the single-cell level. Furthermore, this review describes recent technical advances in IR nanoscopy, and emerging machine learning supported approaches to sampling, signal enhancement, and data processing. This emphasizes that label-free IR nanoscopy holds significant potential for ongoing and future biological applications.