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 Experiment Videos

T-cell activation: a multidimensional signaling network.

Su-Yi Tseng1, Michael L Dustin

  • 1Molecular Pathogenesis Program, Skirball Institute of Biomolecular Medicine, New York University School of Medicine, New York, NY 10016, USA.

Current Opinion in Cell Biology
|September 17, 2002
PubMed
Summary
This summary is machine-generated.

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

Human CD8-iTreg are potent GVHD suppressors and tumoricidal effectors by release of Granzyme-K <sup>+</sup> Supramolecular Attack Particles.

bioRxiv : the preprint server for biology·2026
Same author

PTPN22 regulates T cell synapse formation through PSTPIP1-dependent actin remodeling.

Science signaling·2026
Same author

PD-1 signaling and PD-1 blockade-mediated tumor control are established at microvillar T cell contacts.

Science immunology·2026
Same author

Kv1.3 palmitoylation regulates spatial distribution and channel removal from the immunological synapse.

Cellular and molecular life sciences : CMLS·2026
Same author

isMap - immunological synapse map analysis program.

Frontiers in immunology·2026
Same author

Mixed-mobility supported lipid bilayers uncover the role of immobilized ICAM1 on T cell activation and immune synapse organization.

Proceedings of the National Academy of Sciences of the United States of America·2026
Same journal

Mechanosensing in immune cells: Implications for migration and beyond.

Current opinion in cell biology·2026
Same journal

Emerging role of organelles in cell migration.

Current opinion in cell biology·2026
Same journal

Nuclear adaptation in cell migration.

Current opinion in cell biology·2026
Same journal

Patterns in motion: Choreographing dynamic cell behaviours during tissue repair.

Current opinion in cell biology·2026
Same journal

Quo vadis reconstituted cell surfaces? Purpose and future perspectives for minimal systems of the cell plasma membrane.

Current opinion in cell biology·2026
Same journal

Nuclear determinants of mRNA and protein isoforms.

Current opinion in cell biology·2026
See all related articles

Naïve T cell activation depends on interactions between antigen receptors, adhesion molecules, and co-stimulatory molecules. These interactions form a stable immunological synapse, pausing T cell migration for sustained signaling.

Area of Science:

  • Immunology
  • Cell Biology
  • Molecular Biology

Background:

  • Naïve T cell activation is a critical process for adaptive immunity.
  • This activation relies on the coordinated function of multiple cell surface molecules.
  • Understanding the spatial and temporal dynamics of these interactions is key to T cell function.

Purpose of the Study:

  • To elucidate the role of antigen receptors and adhesion molecules in forming a stable immunological synapse.
  • To investigate how this stable junction impacts T cell migration and signaling.
  • To characterize the temporal regulation of co-stimulatory receptor signaling within the synapse.

Main Methods:

  • Utilized advanced microscopy techniques to observe T cell interactions in real-time.
  • Analyzed the spatio-temporal dynamics of antigen receptors and adhesion molecules during synapse formation.

Related Experiment Videos

  • Investigated the duration and regulation of co-stimulatory signaling within the established immunological synapse.
  • Main Results:

    • Antigen receptors and adhesion molecules cooperate to drive the formation of a stable immunological synapse.
    • Synapse formation leads to the interruption of T cell migration.
    • The stable synapse serves as a platform for sustained, temporally regulated co-stimulatory signaling over several days.

    Conclusions:

    • The formation of a stable immunological synapse is a crucial step in naïve T cell activation.
    • This process involves the precise interplay of antigen receptors and adhesion molecules, leading to altered cell motility.
    • The synapse facilitates prolonged co-stimulatory signaling essential for effective T cell responses.