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Lipton, D. M.

Publications and source records attributed to Lipton, D. M..

2 recordsLinked to original sources

Striatal calcium transients detected by fiber photometry propagate to axons

ARISING FROM: A. Legaria et al., Nature Neuroscience https://doi.org/10.1038/s41593-022-01152-z (2022). Calcium fiber photometry is a popular technique for recording the activity of neuronal populations defined by their gene expression or connectivity. In a recent study, Legaria et al., present evidence that the calcium signal recorded with fiber photometry primarily reports local fluctuations in neuropil Ca2+, rather than somatic Ca2+ influx corresponding to neural firing, as has been assumed by the field. This raises the question of whether fiber photometry transients are a valid measure of the propagation of information from neural soma to their axons. We addressed this question directly, recording coincident activity from both the somato-dendritic region and downstream axons of striatal neural populations. Our findings demonstrate that calcium events are reliably propagated to axons, supporting the interpretation that these events reflect neuronal firing.

neuroscience↗

Axonal transport and active zone proteins regulate dopaminergic synapse formation

At a typical synapse, the precise juxtaposition between the active zone and postsynaptic receptors ensures local and precise neurotransmitter release and detection. Dopamine neurons release neurotransmitter more diffusely using volume-transmission, where precise pre- and post-synaptic alignment is lacking. It is unknown whether Dopaminergic presynaptic terminals have typical active zone structures and how they develop. Here we show that presynaptic terminals of the C. elegans dopaminergic neuron PDE contain bona fide AZ proteins, including SYD-2/Liprin-, ELKS-1, UNC-10/RIM and CLA-1/Piccolo. During development, synaptic vesicles (SVs) and active zone proteins (AZs) coalesce within minutes behind the advancing growth cone. Precise regulation of UNC-104/Kinesin-3-mediated SV transport through kinesin autoinhibition is required to pause transported SVs at synapses. SYD-1 and SYD-2 recruit and cluster the transiting SVs, while ELKS-1 aggregates through a distinct mechanism.

neuroscience↗