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

Gap junctions and connexins: potential contributors to the immunological synapse.

Ernesto Oviedo-Orta1, W Howard Evans

  • 1Bristol Heart Institute, Bristol Royal Infirmary, United Kingdom. e.oviedo-orta@bristol.ac.uk

Journal of Leukocyte Biology
|October 16, 2002
PubMed
Summary

Lymphocytes utilize connexins (protein building blocks of gap junctions) for intercellular communication. These connexins influence immune responses by regulating the release of signaling molecules, impacting lymphocyte function.

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

Effectiveness of Casirivimab and Imdevimab Antibody Combination in Immunocompromised Hospitalized Patients With Coronavirus Disease 2019: A Post Hoc Analysis in a Phase 1/2/3 Double-Blind Trial.

Open forum infectious diseases·2023
Same author

Compassionate Use of REGEN-COV® in Patients With Coronavirus Disease 2019 (COVID-19) and Immunodeficiency-Associated Antibody Disorders.

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America·2021
Same author

Safety, immunogenicity, and efficacy of a Clostridioides difficile toxoid vaccine candidate: a phase 3 multicentre, observer-blind, randomised, controlled trial.

The Lancet. Infectious diseases·2020
Same author

Correction to: Proteomic identification and characterization of hepatic glyoxalase 1 dysregulation in non-alcoholic fatty liver disease.

Proteome science·2018
Same author

Proteomic identification and characterization of hepatic glyoxalase 1 dysregulation in non-alcoholic fatty liver disease.

Proteome science·2018
Same author

Design and evaluation of the immunogenicity and efficacy of a biomimetic particulate formulation of viral antigens.

Scientific reports·2017

Area of Science:

  • Immunology
  • Cell Biology
  • Biochemistry

Background:

  • Gap junctional communication facilitates metabolic coupling between adjacent cells.
  • Lymphocytes express connexins, the protein components of gap junctions, including connexin 40 and connexin 43.
  • Connexins are implicated in lymphocyte physiology, influencing immunoglobulin and cytokine secretion.

Purpose of the Study:

  • To investigate the role of connexins and gap junctional communication in lymphocyte function.
  • To explore the potential paracrine functions of lymphocyte connexins beyond traditional gap junctions.
  • To understand the contribution of lymphocyte gap junctional communication to the immunological synapse.

Main Methods:

  • Utilized connexin mimetic peptides to inhibit gap junctional communication in T and B lymphocyte cocultures.

Related Experiment Videos

  • Analyzed the effects of inhibition on immunoglobulin and cytokine secretion.
  • Examined the potential involvement of gap junction hemichannels in metabolite release.
  • Main Results:

    • Inhibitors of gap junctional communication reduced immunoglobulin and cytokine secretion by lymphocytes.
    • Evidence suggests connexins may have paracrine functions through hemichannel activity, releasing molecules like ATP.
    • Connexins are increasingly recognized for their role in lymphocyte signaling.

    Conclusions:

    • Connexins play a fundamental role in lymphocyte physiology and immune responses.
    • Lymphocyte connexins may function not only in gap junctions but also via hemichannels, mediating paracrine signaling.
    • Gap junctional communication is a significant component of the complex signaling network within the immunological synapse.