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-lymphocyte coactivator molecules.

L I Salazar-Fontana1, B E Bierer

  • 1Laboratory of Lymphocyte Biology, National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, Maryland 20892, USA.

Current Opinion in Hematology
|January 4, 2001
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

Ethical Challenges in Clinical Research During the COVID-19 Pandemic.

Journal of bioethical inquiry·2020
Same author

T cell regulation of p62(dok) (Dok1) association with Crk-L.

The Journal of biological chemistry·2001
Same author

A multicenter, randomized, double-blind comparison of different doses of intravenous immunoglobulin for prevention of graft-versus-host disease and infection after allogeneic bone marrow transplantation.

Bone marrow transplantation·2001
Same author

T cell signal transduction and the role of CD7 in costimulation.

Immunologic research·2001
Same author

Cell surface CD28 levels define four CD4+ T cell subsets: abnormal expression in rheumatoid arthritis.

Clinical immunology (Orlando, Fla.)·2001
Same author

The actin cytoskeleton, membrane lipid microdomains, and T cell signal transduction.

Advances in immunology·2001

T-cell activation relies on the T-cell receptor (TCR) and costimulatory molecules like CD28 within the immunologic synapse. Novel costimulatory receptors influence T-cell differentiation, activation, and effector functions, impacting B-cell responses.

Area of Science:

  • Immunology
  • Cellular Biology
  • Molecular Biology

Background:

  • T-cell recognition and activation occur at the immunologic synapse, a specialized contact area enriched in glycolipid membrane microdomains.
  • T-cell activation requires specific peptide-antigen recognition via the T-cell receptor (TCR) and engagement with major histocompatibility complex (MHC) molecules.
  • TCR engagement alone can lead to T-cell unresponsiveness, but coreceptor CD28 ligation prevents this, highlighting the importance of costimulatory signals.

Purpose of the Study:

  • To investigate the role of novel costimulatory molecules in T-cell activation and differentiation.
  • To understand how these receptors influence T-cell effector functions and B-cell responses.

Main Methods:

  • The study involved the identification and characterization of novel costimulatory molecules.

Related Experiment Videos

  • Analysis of their roles in T-cell differentiation and activation pathways.
  • Assessment of their impact on T-cell effector functions and B-cell differentiation and function.
  • Main Results:

    • Novel costimulatory molecules from the CD28 and TNF/TNFR superfamilies have been identified.
    • These receptors modulate T-cell activation at various differentiation stages.
    • They play significant roles in promoting distinct T-cell effector functions and are crucial for B-cell differentiation and function.

    Conclusions:

    • Costimulatory receptors are critical regulators of T-cell activation, differentiation, and function.
    • Novel costimulatory molecules expand our understanding of immune responses.
    • These findings have implications for immune modulation and therapeutic strategies.