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Chrapkiewicz, R.

Publications and source records attributed to Chrapkiewicz, R..

4 recordsLinked to original sources

Multimodal alignments of in vivo imaging and spatial biology datasets at cellular resolution

Parallel revolutions in intravital microscopy and spatial biology techniques have respectively enabled large-scale recordings of cellular dynamics in live animals and multi-dimensional molecular profiling at single-cell resolution. However, due to the challenges of aligning data from different modalities at cellular resolution, these two transformational approaches have generally been applied on separate biological samples, stymying the ability to link activity patterns and molecular attributes in the same exact cells. To enable routine, multimodal investigations of cells in vivo dynamics and molecular content, we created TRU-FACT (Total Registration Under Functional Activity, Connectivity, and Transcriptomics), a broadly applicable experimental and computational pipeline for registering large populations of individual cells across intravital imaging and spatial biology datasets. The pipeline combines three key innovations: an optomechanical tissue handling and alignment method to parallelize specimen planes, a graph-theoretic method to register individual cells based on their geometric relationships to neighboring cells, and a statistical framework that provides for each cell an a posteriori probability of correct registration. We validated TRU-FACT with several preparations for imaging neural Ca2+ activity in cortical and deep brain areas in head-fixed and freely behaving mice, RNA-barcode-expressing viruses for labeling neural projections, and low- and high-plex spatial transcriptomic methods. In mice performing a skilled reaching task, TRU-FACT alignments revealed the movement-related signaling patterns of intratelencephalic, extratelencephalic, and striatum-, superior colliculus-, and thalamus-projecting motor cortical neurons. Overall, TRU-FACT constitutes a scalable, multimodal discovery platform that is applicable to diverse tissue-types and spatial biology techniques, thereby enabling multiscale analyses of many complex biological systems.

neuroscience↗

Striatal neural ensemble codes for voluntary locomotor and involuntary dyskinetic movements

BackgroundIn the classical model of basal ganglia circuitry, striatal spiny projection neurons of the direct and indirect pathways (dSPNs, iSPNs) promote and suppress movement, respectively, and exhibit unbalanced activity levels during hypokinetic or hyperkinetic conditions. Most therapies for these conditions are thought to work by rebalancing the relative activity of dSPNs and iSPNs towards normal levels. However, the mechanism of amantadine, which uniquely improves both hypokinetic and hyperkinetic conditions, is poorly understood. ObjectiveTo determine whether amantadine restores motor function by normalizing the balance of dSPN and iSPN activity or through a distinct mechanism. MethodsWe used dual-color two-photon Ca2+ imaging in the 6-OHDA mouse model of Parkinsons disease to concurrently monitor dSPN and iSPN dynamics across healthy, hypokinetic (parkinsonian), and hyperkinetic (dyskinetic) conditions. ResultsWe evaluated both dSPN/iSPN activity balance and action-specific neural ensemble activity in the dorsolateral striatum. In hypokinetic conditions, L-DOPA rescued the dSPN/iSPN imbalance but failed to restore the disrupted activity of the locomotion-specific ensemble. Conversely, amantadine improved locomotion-specific ensemble activity without normalizing the dSPN/iSPN imbalance. In hyperkinetic conditions, forelimb dyskinesias were characterized by neural activity patterns distinct from those encoding locomotion. Amantadine selectively suppressed the resting activity of forelimb dyskinesia ensembles without affecting locomotion-coding ensembles or restoring pathway balance. ConclusionsL-DOPA and amantadine may act through distinct mechanisms, with L-DOPA normalizing pathway balance and amantadine modulating action-specific neural ensembles. These findings support the importance of action-coding disruptions during hypokinetic and hyperkinetic conditions and suggest that correcting them can restore motor function.

neuroscience↗

Imaging high-frequency voltage dynamics in multiple neuron classes of behaving mammals

Fluorescent genetically encoded voltage indicators report transmembrane potentials of targeted cell-types. However, voltage-imaging instrumentation has lacked the sensitivity to track spontaneous or evoked high-frequency voltage oscillations in neural populations. Here we describe two complementary TEMPO voltage-sensing technologies that capture neural oscillations up to [~]100 Hz. Fiber-optic TEMPO achieves [~]10-fold greater sensitivity than prior photometry systems, allows hour-long recordings, and monitors two neuron-classes per fiber-optic probe in freely moving mice. With it, we uncovered cross-frequency-coupled theta- and gamma-range oscillations and characterized excitatory-inhibitory neural dynamics during hippocampal ripples and visual cortical processing. The TEMPO mesoscope images voltage activity in two cell-classes across a [~]8-mm-wide field-of-view in head-fixed animals. In awake mice, it revealed sensory-evoked excitatory-inhibitory neural interactions and traveling gamma and 3-7 Hz waves in the visual cortex, and previously unreported propagation directions for hippocampal theta and beta waves. These technologies have widespread applications probing diverse oscillations and neuron-type interactions in healthy and diseased brains.

neuroscience↗

Dual polarity voltage imaging reveals subthreshold dynamics and concurrent spiking patterns of multiple neuron-types

Genetically encoded fluorescent voltage indicators are ideally suited to reveal the millisecond-scale interactions among and between distinct, targeted cell populations. However, current indicator families lack the requisite sensitivity for in vivo multipopulation imaging. We describe high-performance green and red sensors, Ace-mNeon2 and VARNAM2, and their reverse response-polarity variants, pAce and pAceR. Our indicators enable 0.4-1 kHz voltage recordings from >50 neurons per field-of-view in awake mice and [~]30-min continuous imaging in flies. Using dual-polarity multiplexed imaging, we uncovered behavioral state-dependent interactions between distinct neocortical subclasses, as well as contributions to hippocampal field potentials from non-overlapping projection neuronal ensembles. By combining three mutually compatible indicators, we demonstrate concurrent triple-population voltage imaging. Our approach will empower investigations of the dynamic interplay between neuronal subclasses at single-spike resolution. One Sentence SummaryA new suite of voltage sensors enables simultaneous cellular-resolution activity imaging from multiple, targeted neuron-types in awake animals.

neuroscience↗