Browse
Submit Data
Databases
API
Help

Dataset Information

25 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Imaging Action Potential in Single Mammalian Neurons by Tracking the Accompanying Sub-Nanometer Mechanical Motion.

ABSTRACT: Action potentials in neurons have been studied traditionally by intracellular electrophysiological recordings and more recently by the fluorescence detection methods. Here we describe a label-free optical imaging method that can measure mechanical motion in single cells with a sub-nanometer detection limit. Using the method, we have observed sub-nanometer mechanical motion accompanying the action potential in single mammalian neurons by averaging the repeated action potential spikes. The shape and width of the transient displacement are similar to those of the electrically recorded action potential, but the amplitude varies from neuron to neuron, and from one region of a neuron to another, ranging from 0.2-0.4 nm. The work indicates that action potentials may be studied noninvasively in single mammalian neurons by label-free imaging of the accompanying sub-nanometer mechanical motion.

SUBMITTER: Yang Y

PROVIDER: S-EPMC6141446 | biostudies-literature | 2018 May

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Publications

Imaging Action Potential in Single Mammalian Neurons by Tracking the Accompanying Sub-Nanometer Mechanical Motion.

Yang Yunze Y Liu Xian-Wei XW Wang Hui H Yu Hui H Guan Yan Y Wang Shaopeng S Tao Nongjian N

ACS nano 20180328 5

Action potentials in neurons have been studied traditionally by intracellular electrophysiological recordings and more recently by the fluorescence detection methods. Here we describe a label-free optical imaging method that can measure mechanical motion in single cells with a sub-nanometer detection limit. Using the method, we have observed sub-nanometer mechanical motion accompanying the action potential in single mammalian neurons by averaging the repeated action potential spikes. The shape a ...[more]

PMID: 29570267

Similar Datasets

Nanometer-scale imaging by the modulation tracking method.

Project description:We developed an optical imaging method based on a feedback principle in which the specific scan pattern is adapted according to the shape of the sample. The feedback approach produces nanometer-resolved 3D images of very small and moving features in live cells in seconds. We show images of microvilli in live cultured opossum kidney cells expressing NaPi co-transporter proteins with different GFP constructs and images of cell protrusions in a collagen matrix with a resolution of about 20 nm. We found that in the microvilli the NaPi proteins can be found clustered. Along cell protrusions in 3D we identified cellular adhesions to the extracellular matrix. Our approach to super-resolution and to 3D nanoimaging is different than other proposed methods that break the diffraction limit using non-linear effects or are based on single molecule localization.

| S-EPMC3393040 | biostudies-literature

Tracking individual action potentials throughout mammalian axonal arbors.

Project description:Axons are neuronal processes specialized for conduction of action potentials (APs). The timing and temporal precision of APs when they reach each of the synapses are fundamentally important for information processing in the brain. Due to small diameters of axons, direct recording of single AP transmission is challenging. Consequently, most knowledge about axonal conductance derives from modeling studies or indirect measurements. We demonstrate a method to noninvasively and directly record individual APs propagating along millimeter-length axonal arbors in cortical cultures with hundreds of microelectrodes at microsecond temporal resolution. We find that cortical axons conduct single APs with high temporal precision (~100 µs arrival time jitter per mm length) and reliability: in more than 8,000,000 recorded APs, we did not observe any conduction or branch-point failures. Upon high-frequency stimulation at 100 Hz, successive became slower, and their arrival time precision decreased by 20% and 12% for the 100th AP, respectively.

| S-EPMC5633342 | biostudies-literature

Deep Predictive Motion Tracking in Magnetic Resonance Imaging: Application to Fetal Imaging.

Project description:Fetal magnetic resonance imaging (MRI) is challenged by uncontrollable, large, and irregular fetal movements. It is, therefore, performed through visual monitoring of fetal motion and repeated acquisitions to ensure diagnostic-quality images are acquired. Nevertheless, visual monitoring of fetal motion based on displayed slices, and navigation at the level of stacks-of-slices is inefficient. The current process is highly operator-dependent, increases scanner usage and cost, and significantly increases the length of fetal MRI scans which makes them hard to tolerate for pregnant women. To help build automatic MRI motion tracking and navigation systems to overcome the limitations of the current process and improve fetal imaging, we have developed a new real-time image-based motion tracking method based on deep learning that learns to predict fetal motion directly from acquired images. Our method is based on a recurrent neural network, composed of spatial and temporal encoder-decoders, that infers motion parameters from anatomical features extracted from sequences of acquired slices. We compared our trained network on held-out test sets (including data with different characteristics, e.g. different fetuses scanned at different ages, and motion trajectories recorded from volunteer subjects) with networks designed for estimation as well as methods adopted to make predictions. The results show that our method outperformed alternative techniques, and achieved real-time performance with average errors of 3.5 and 8 degrees for the estimation and prediction tasks, respectively. Our real-time deep predictive motion tracking technique can be used to assess fetal movements, to guide slice acquisitions, and to build navigation systems for fetal MRI.

| S-EPMC7787194 | biostudies-literature

MINFLUX nanometer-scale 3D imaging and microsecond-range tracking on a common fluorescence microscope.

Project description:The recently introduced minimal photon fluxes (MINFLUX) concept pushed the resolution of fluorescence microscopy to molecular dimensions. Initial demonstrations relied on custom made, specialized microscopes, raising the question of the method's general availability. Here, we show that MINFLUX implemented with a standard microscope stand can attain 1-3 nm resolution in three dimensions, rendering fluorescence microscopy with molecule-scale resolution widely applicable. Advances, such as synchronized electro-optical and galvanometric beam steering and a stabilization that locks the sample position to sub-nanometer precision with respect to the stand, ensure nanometer-precise and accurate real-time localization of individually activated fluorophores. In our MINFLUX imaging of cell- and neurobiological samples, ~800 detected photons suffice to attain a localization precision of 2.2 nm, whereas ~2500 photons yield precisions <1 nm (standard deviation). We further demonstrate 3D imaging with localization precision of ~2.4 nm in the focal plane and ~1.9 nm along the optic axis. Localizing with a precision of <20 nm within ~100 µs, we establish this spatio-temporal resolution in single fluorophore tracking and apply it to the diffusion of single labeled lipids in lipid-bilayer model membranes.

| S-EPMC7935904 | biostudies-literature

Different but complementary roles of action and gaze in action observation priming: Insights from eye- and motion-tracking measures.

Project description:Action priming following action observation is thought to be caused by the observed action kinematics being represented in the same brain areas as those used for action execution. But, action priming can also be explained by shared goal representations, with compatibility between observation of the agent's gaze and the intended action of the observer. To assess the contribution of action kinematics and eye-gaze cues in the prediction of an agent's action goal and action priming, participants observed actions where the availability of both cues was manipulated. Action observation was followed by action execution, and the congruency between the target of the agent's and observer's actions, and the congruency between the observed and executed action spatial location were manipulated. Eye movements were recorded during the observation phase, and the action priming was assessed using motion analysis. The results showed that the observation of gaze information influenced the observer's prediction speed to attend to the target, and that observation of action kinematic information influenced the accuracy of these predictions. Motion analysis results showed that observed action cues alone primed both spatial incongruent and object congruent actions, consistent with the idea that the prime effect was driven by similarity between goals and kinematics. The observation of action and eye-gaze cues together induced a prime effect complementarily sensitive to object and spatial congruency. While observation of the agent's action kinematics triggered an object-centered and kinematic-centered action representation, independently, the complementary observation of eye-gaze triggered a more fine-grained representation illustrating a specification of action kinematics toward the selected goal. Even though both cues differentially contributed to action priming, their complementary integration led to a more refined pattern of action priming.

| S-EPMC4419854 | biostudies-literature

Label-Free Tracking of Single Organelle Transportation in Cells with Nanometer Precision Using a Plasmonic Imaging Technique.

Project description:Imaging and tracking of nano- and micrometer-sized organelles in cells with nanometer precision is crucial for understanding cellular behaviors at the molecular scale. Because of the fast intracellular dynamic processes, the imaging and tracking method must also be fast. In addition, to ensure that the observed dynamics is relevant to the native functions, it is critical to keep the cells under their native states. Here, a plasmonics-based imaging technique is demonstrated for studying the dynamics of organelles in 3D with high localization precision (5 nm) and temporal (10 ms) resolution. The technique is label-free and can track subcellular structures in the native state of the cells. Using the technique, nanometer steps of organelle (e.g., mitochondria) transportation are observed along neurite microtubules in primary neurons, and the 3D structure of neurite microtubule bundles is reconstructed at the nanometer scale from the tracks of the moving organelles.

| S-EPMC4474744 | biostudies-literature

MR acoustic radiation force imaging: in vivo comparison to ultrasound motion tracking.

Project description:MR acoustic radiation force (ARF) imaging was developed for measuring tiSsue elastic properties using focused ultrasound to deliver a localized tissue motion. In this study, an imaging ultrasound transducer was mounted on the focused ultrasound transducer and ultrasound motion tracking was performed simultaneously to MR ARF imaging to validate the measurement results. In vivo studies on rabbit thigh muscle were performed and results showed a general agreement between the two modalities (slope=0.96 and R2=0.67). The temporal information by the ultrasound measurement indicates that the parameters in MR ARF imaging should be optimized according to the tissue type, acoustic power, and envelope and frequency of the ARF modulation.

| S-EPMC2832062 | biostudies-literature

Real-time eye motion compensation for OCT imaging with tracking SLO.

Project description:Fixational eye movements remain a major cause of artifacts in optical coherence tomography (OCT) images despite the increases in acquisition speeds. One approach to eliminate the eye motion is to stabilize the ophthalmic imaging system in real-time. This paper describes and quantifies the performance of a tracking OCT system, which combines a phase-stabilized optical frequency domain imaging (OFDI) system and an eye tracking scanning laser ophthalmoscope (TSLO). We show that active eye tracking minimizes artifacts caused by eye drift and micro saccades. The remaining tracking lock failures caused by blinks and large saccades generate a trigger signal which signals the OCT system to rescan corrupted B-scans. Residual motion artifacts in the OCT B-scans are reduced to 0.32 minutes of arc (~1.6 µm) in an in vivo human eye enabling acquisition of high quality images from the optic nerve head and lamina cribrosa pore structure.

| S-EPMC3493227 | biostudies-other

Motion tracking of parents' infant- versus adult-directed actions reveals general and action-specific modulations.

Project description:Parents tend to modulate their movements when demonstrating actions to their infants. Thus far, these modulations have primarily been quantified by human raters and for entire interactions, thereby possibly overlooking the intricacy of such demonstrations. Using optical motion tracking, the precise modulations of parents' infant-directed actions were quantified and compared to adult-directed actions and between action types. Parents demonstrated four novel objects to their 14-month-old infants and adult confederates. Each object required a specific action to produce a unique effect (e.g. rattling). Parents were asked to demonstrate an object at least once before passing it to their demonstration partner, and they were subsequently free to exchange the object as often as desired. Infants' success at producing the objects' action-effects was coded during the demonstration session and their memory of the action-effects was tested after a several-minute delay. Indicating general modulations across actions, parents repeated demonstrations more often, performed the actions in closer proximity and demonstrated action-effects for longer when interacting with their infant compared to the adults. Meanwhile, modulations of movement size and velocity were specific to certain action-effect pairs. Furthermore, a 'just right' modulation of proximity was detected, since infants' learning, memory, and parents' prior evaluations of their infants' motor abilities, were related to demonstrations that were performed neither too far from nor too close to the infants. Together, these findings indicate that infant-directed action modulations are not solely overall exaggerations but are dependent upon the characteristics of the to-be learned actions, their effects, and the infant learners.

| S-EPMC6916206 | biostudies-literature

Tracking Local Mechanical Impact in Heterogeneous Polymers with Direct Optical Imaging.

Project description:Structural heterogeneity defines the properties of many functional polymers and it is often crucial for their performance and ability to withstand mechanical impact. Such heterogeneity, however, poses a tremendous challenge for characterization of these materials and limits our ability to design them rationally. Herein we present a practical methodology capable of resolving the complex mechanical behavior and tracking mechanical impact in discrete phases of segmented polyurethane-a typical example of a structurally complex polymer. Using direct optical imaging of photoluminescence produced by a small-molecule organometallic mechano-responsive sensor we observe in real time how polymer phases dissipate energy, restructure, and breakdown upon mechanical impact. Owing to its simplicity and robustness, this method has potential in describing the evolution of complex soft-matter systems for which global characterization techniques fall short of providing molecular-level insight.

| S-EPMC6348422 | biostudies-literature

OmicsDI is part of the ELIXIR infrastructure

OmicsDI is an Elixir interoperability service. Learn more ›

Tweets

OmicsDI Databases

PRIDE
PeptideAtlas
MassIVE
JPOST Repository
Physiome Model Repository

EGA
EVA
ENA
LINCS
PAXDB
Cell Collective

MetaboLights
Metabolomics Workbench
MetabolomeExpress
GNPS
BioModels
FAIRDOMHub

ArrayExpress
dbGaP
ExpressionAtlas
GEO
NODE

Information

Databases
Help
API
Contact us
Code on GitHub
Terms of use
Submit Data