Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Selective Enrichment of Non-Canonical Vγ9-Jγ2 TRG Clonotypes in Clear Cell Renal Cell Carcinoma With Shorter CDR3 Loops.

Immune network·2026
Same author

Multi-Model Machine Learning for Survival Predictions for Castration-Resistant Prostate Cancer.

Cancers·2026
Same author

Predictive value of primary tumour SUV<sub>max</sub> on <sup>18</sup>F-fluoro-2-deoxy-D-glucose positron emission tomography/computed tomography in patients undergoing fertility-sparing treatment for early endometrial cancer.

European journal of obstetrics, gynecology, and reproductive biology·2026
Same author

A microscopic computational simulation of [<sup>18</sup>F]FDG transport and metabolism identifies valid regimes for compartmental analysis.

Physics in medicine and biology·2026
Same author

A parametric study of mechanoporation through microfluidic design to modulate shear, compressive, and adhesion forces and loading rates.

Lab on a chip·2026
Same author

In Regard to Pratx et al.

International journal of radiation oncology, biology, physics·2026

Related Experiment Video

Updated: Apr 20, 2026

Tracking Mouse Bone Marrow Monocytes In Vivo
12:08

Tracking Mouse Bone Marrow Monocytes In Vivo

Published on: February 27, 2015

10.1K

Single-cell tracking with PET using a novel trajectory reconstruction algorithm.

Keum Sil Lee, Tae Jin Kim, Guillem Pratx

    IEEE Transactions on Medical Imaging
    |November 26, 2014
    PubMed
    Summary

    Researchers developed a new computational method to track individual radiolabeled cells directly from PET data, moving beyond traditional image-based analysis to improve precision in cell migration studies.

    Keywords:
    Cell TrackingList-mode DataMonte Carlo SimulationSmall-animal Imaging

    Frequently Asked Questions

    More Related Videos

    3D Orbital Tracking in a Modified Two-photon Microscope: An Application to the Tracking of Intracellular Vesicles
    11:28

    3D Orbital Tracking in a Modified Two-photon Microscope: An Application to the Tracking of Intracellular Vesicles

    Published on: October 1, 2014

    10.7K
    Isolation and Time-Lapse Imaging of Primary Mouse Embryonic Palatal Mesenchyme Cells to Analyze Collective Movement Attributes
    07:13

    Isolation and Time-Lapse Imaging of Primary Mouse Embryonic Palatal Mesenchyme Cells to Analyze Collective Movement Attributes

    Published on: February 13, 2021

    2.7K

    Related Experiment Videos

    Last Updated: Apr 20, 2026

    Tracking Mouse Bone Marrow Monocytes In Vivo
    12:08

    Tracking Mouse Bone Marrow Monocytes In Vivo

    Published on: February 27, 2015

    10.1K
    3D Orbital Tracking in a Modified Two-photon Microscope: An Application to the Tracking of Intracellular Vesicles
    11:28

    3D Orbital Tracking in a Modified Two-photon Microscope: An Application to the Tracking of Intracellular Vesicles

    Published on: October 1, 2014

    10.7K
    Isolation and Time-Lapse Imaging of Primary Mouse Embryonic Palatal Mesenchyme Cells to Analyze Collective Movement Attributes
    07:13

    Isolation and Time-Lapse Imaging of Primary Mouse Embryonic Palatal Mesenchyme Cells to Analyze Collective Movement Attributes

    Published on: February 13, 2021

    2.7K

    Area of Science:

    • Medical imaging physics and Positron Emission Tomography tracking research
    • Biomedical engineering and computational algorithm development

    Background:

    Traditional biomedical imaging relies on static distributions of radiotracers to visualize biological processes. This paradigm often fails when monitoring the dynamic movement of individual cells within a living subject. No prior work had resolved how to bypass standard image reconstruction for tracking applications. That uncertainty drove the need for a direct data-processing approach. Prior research has shown that standard methods struggle to capture rapid cellular motion accurately. This gap motivated the development of specialized algorithms designed for list-mode data. Investigators sought to improve upon existing particle tracking techniques by modeling motion as a continuous function. This study addresses the limitations of conventional visualization by focusing on trajectory reconstruction instead of static snapshots.

    Purpose Of The Study:

    The researchers aimed to develop a new algorithm for reconstructing the trajectory of a single moving cell. They sought to move beyond the standard imaging paradigm that represents radiotracer distributions. This study addresses the limitations of using static images for tracking dynamic biological processes. The investigators focused on reconstructing time-varying positions directly from raw measurement data. They intended to provide a more optimal approach for cell tracking applications in biomedical research. The team formulated a mathematical model to represent motion as a continuous function. This effort was motivated by the need for higher precision in monitoring individual cells. The study establishes a proof of concept for direct list-mode data processing in PET systems.

    Main Methods:

    The research team formulated a novel algorithm to process list-mode coincidence events. They modeled the movement path as a three-dimensional B-spline function of time. The investigators applied nonlinear optimization to minimize the distance between the path and recorded events. Review approach involved using Monte Carlo simulations to evaluate performance within a small-animal system. The scientists compared their results against conventional maximum likelihood expectation maximization techniques. They also assessed the method against the minimum distance strategy typically used for particle tracking. Experimental data acquisition provided a secondary validation for the proposed computational framework. This systematic evaluation ensured the reliability of the tracking accuracy across different test scenarios.

    Main Results:

    The algorithm tracks a single source with 3 mm accuracy in small-animal systems. This performance occurs when the cell activity in Becquerels exceeds four times its velocity in millimeters per second. The new method consistently outperforms conventional maximum likelihood expectation maximization approaches. It also shows superior results compared to the minimum distance method used in particle tracking. Researchers successfully validated the model using experimentally acquired data. The findings confirm the feasibility of tracking at the whole-body level. The study demonstrates that direct processing of list-mode data is effective for physiologically relevant parameters. These results highlight the potential of bypassing standard image reconstruction for dynamic cellular monitoring.

    Conclusions:

    The authors demonstrated the feasibility of tracking a single moving cell directly from list-mode data. This approach functions effectively at the whole-body level for physiologically relevant activities and velocities. The proposed algorithm provides a viable alternative to standard image-based representations for cell migration studies. Researchers showed that the method maintains 3 mm accuracy under specific activity-to-velocity conditions. The study confirms that direct trajectory modeling outperforms conventional maximum likelihood expectation maximization techniques. The findings also indicate superior performance compared to existing minimum distance methods used in particle tracking. This work establishes a new framework for monitoring cellular dynamics without relying on traditional image reconstruction. These results suggest that direct data processing enhances the precision of tracking moving sources in small-animal systems.

    The researchers propose a 3-D B-spline function to model motion. This approach minimizes the mean-square distance between the trajectory and recorded coincidence events, outperforming the conventional maximum likelihood expectation maximization technique used in standard imaging.

    The study utilizes GATE, which stands for Geant4 Application for Tomographic Emission. This Monte Carlo simulation tool allows researchers to model the interaction of radiation within a small-animal system to validate the trajectory reconstruction accuracy.

    A cell must maintain an activity level in Becquerels greater than four times its velocity in millimeters per second. This condition is necessary to achieve the reported 3 mm spatial accuracy within the small-animal system.

    List-mode data serves as the primary input for the trajectory reconstruction. Unlike standard image-based approaches, this data type allows the algorithm to process individual coincidence events directly to determine the source position over time.

    The algorithm achieves a spatial accuracy of 3 mm. This measurement represents the precision of the reconstructed trajectory when the cell activity exceeds the threshold relative to its movement speed.

    The authors propose that this method enables whole-body tracking of moving cells. They suggest this approach is superior to the minimum distance method traditionally applied in positron emission particle tracking for monitoring cellular dynamics.