science pharmaceutical expo biotech jobs

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Oviedo-Orta, E.
Right arrow Articles by Evans, W. H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Oviedo-Orta, E.
Right arrow Articles by Evans, W. H.
(Journal of Leukocyte Biology. 2002;72:636-642.)
© 2002 by Society for Leukocyte Biology

Gap junctions and connexins: potential contributors to the immunological synapse

Ernesto Oviedo-Orta* and W. Howard Evans{dagger}

* Bristol Heart Institute, Bristol Royal Infirmary, United Kingdom; and
{dagger} Department of Medical Biochemistry and Wales Heart Research Institute, University of Wales College of Medicine, Cardiff, United Kingdom

Correspondence: Ernesto Oviedo-Orta, Bristol Heart Institute, Bristol Royal Infirmary, Level 7, Upper Maudlin Street, Bristol BS2 8HW, UK. E-mail: e.oviedo-orta{at}bristol.ac.uk

Gap junctional communication is a widespread mechanism for metabolic coupling of adjoining cells. In the immune system, evidence has built up showing that lymphocytes possess the protein building blocks of gap junctions, the connexins. The most widespread is connexin 43, but connexin 40 is also present in secondary lymphoid organs. Inhibitors of gap junctional communication, especially the highly specific connexin mimetic peptides, have been shown to decrease the secretion of immunoglobulins and cytokines by T and B lymphocyte cocultures, indicating that connexins may play a fundamental role in lymphocyte physiology. Traditionally, connexins function when assembled into gap junction-intercellular channels. However, the possibility is now arising that gap junction hemichannels, previously viewed as plasma membrane precursors of gap junctions, are also involved in the release from cells of small metabolites, e.g., adenosine 5'-triphosphate and nicotinamide adenine dinucleotide+, and this opens up a second, possible paracrine function for connexins detected in lymphocytes. The increasing structural and functional evidence points to a potential role that lymphocyte gap junctional intercellular communication may play within the complex signaling components of the immunological synapse.

Key Words: cytometry • antibodies • cell adhesion • inflammation • intercellular communication • immune response • peptides • flow




This article has been cited by other articles:


Home page
Circ. Res.Home page
H. K. Eltzschig, T. Eckle, A. Mager, N. Kuper, C. Karcher, T. Weissmuller, K. Boengler, R. Schulz, S. C. Robson, and S. P. Colgan
ATP Release From Activated Neutrophils Occurs via Connexin 43 and Modulates Adenosine-Dependent Endothelial Cell Function
Circ. Res., November 10, 2006; 99(10): 1100 - 1108.
[Abstract] [Full Text] [PDF]


Home page
Cardiovasc ResHome page
C. W Wong, T. Christen, and B. R Kwak
Connexins in leukocytes: shuttling messages?
Cardiovasc Res, May 1, 2004; 62(2): 357 - 367.
[Abstract] [Full Text] [PDF]