Editorial |
Correspondence to David C. Spray, PhD, Department of Neuroscience, Room 712 Kennedy Center, Albert Einstein College of Medicine, 1410 Pelham Parkway South, Bronx, NY 10461. E-mail spray@aecom.yu.edu
Key Words: gap junction connexin proteolysis endothelium
Gap junction channels are unique. No other channel in vertebrates provides an enclosed conduit for direct diffusional exchange of ions and small molecules between cells, and few other membrane channels have pore diameters large enough to accommodate passage of metabolites and signaling molecules with molecular weights as high as 1000 Da. Moreover, as addressed in two articles in this issue of Circulation Research, gap junctions are formed by proteins with unusually rapid turnover times1 and extremely flexible expression patterns.2
The connexin proteins that form gap junction channels are encoded by a gene family with at least 14 members in rodents. Each connexin protein has four transmembrane domains, one intracellular and two extracellular loops, and cytoplasmically located carboxyl and amino termini. Six connexin molecules, most likely arranged so that their third transmembrane domains line the channel lumen, comprise the hemichannels or connexons that are contributed by each cell of the coupled pair. Complete gap junction channels, with connexons docked across the gap of extracellular space by interactions of the extracellular loops, are commonly found clustered together, forming islands of particles or pits in freeze-fractured preparations, linearly apposed but slightly separated membranes in thin-section electron micrographs and macular regions of intercellular immunostaining with gap junction antibodies.
Remarkably, in studies first performed on rat liver in
vivo3 4 and subsequently in cardiac myocytes and
hepatocytes and cell lines in
culture,5 6 7 8 the turnover times for connexin
molecules have been found to be very short. The article by Beardslee et
al1 provides direct evidence for
This article has been cited by other articles:
![]() |
F. Allagnat, D. Martin, D. F. Condorelli, G. Waeber, and J.-A. Haefliger Glucose represses connexin36 in insulin-secreting cells J. Cell Sci., November 15, 2005; 118(22): 5335 - 5344. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. D. Mruk and C. Y. Cheng Sertoli-Sertoli and Sertoli-Germ Cell Interactions and Their Significance in Germ Cell Movement in the Seminiferous Epithelium during Spermatogenesis Endocr. Rev., October 1, 2004; 25(5): 747 - 806. [Abstract] [Full Text] [PDF] |
||||
![]() |
J.-A. Haefliger, P. Nicod, and P. Meda Contribution of connexins to the function of the vascular wall Cardiovasc Res, May 1, 2004; 62(2): 345 - 356. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. Martin, T. Tawadros, L. Meylan, A. Abderrahmani, D. F. Condorelli, G. Waeber, and J.-A. Haefliger Critical Role of the Transcriptional Repressor Neuron-restrictive Silencer Factor in the Specific Control of Connexin36 in Insulin-producing Cell Lines J. Biol. Chem., December 26, 2003; 278(52): 53082 - 53089. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. N. Tulenko Regulating Cross-Talk Between Vascular Smooth Muscle Cells Arterioscler Thromb Vasc Biol, October 1, 2003; 23(10): 1707 - 1709. [Full Text] [PDF] |
||||
![]() |
S. Le Gurun, D. Martin, A. Formenton, P. Maechler, D. Caille, G. Waeber, P. Meda, and J.-A. Haefliger Connexin-36 Contributes to Control Function of Insulin-producing Cells J. Biol. Chem., September 26, 2003; 278(39): 37690 - 37697. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. St-Pierre, J. Dufresne, A. A. Rooney, and D. G. Cyr Neonatal Hypothyroidism Alters the Localization of Gap Junctional Protein Connexin 43 in the Testis and Messenger RNA Levels in the Epididymis of the Rat Biol Reprod, April 1, 2003; 68(4): 1232 - 1240. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. C. Anderson, C. Stone, L. Tkach, and N. SundarRaj Rho and Rho-Kinase (ROCK) Signaling in Adherens and Gap Junction Assembly in Corneal Epithelium Invest. Ophthalmol. Vis. Sci., April 1, 2002; 43(4): 978 - 986. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Stuart-Smith and J. Y. Jeremy Microvessel damage in acute respiratory distress syndrome: the answer may not be NO Br. J. Anaesth., August 1, 2001; 87(2): 272 - 279. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. G. Emerson and S. S. Segal Electrical Coupling Between Endothelial Cells and Smooth Muscle Cells in Hamster Feed Arteries : Role in Vasomotor Control Circ. Res., September 15, 2000; 87(6): 474 - 479. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. A. Cancelas, W. L. M. Koevoet, A. E. de Koning, A. E. M. Mayen, E. J. C. Rombouts, and R. E. Ploemacher Connexin-43 gap junctions are involved in multiconnexin-expressing stromal support of hemopoietic progenitors and stem cells Blood, July 15, 2000; 96(2): 498 - 505. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. L. Sandow and C. E. Hill Incidence of Myoendothelial Gap Junctions in the Proximal and Distal Mesenteric Arteries of the Rat Is Suggestive of a Role in Endothelium-Derived Hyperpolarizing Factor-Mediated Responses Circ. Res., February 18, 2000; 86(3): 341 - 346. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. W. Ashton, R. Yokota, G. John, S. Zhao, S. O. Suadicani, D. C. Spray, and J. A. Ware Inhibition of Endothelial Cell Migration, Intercellular Communication, and Vascular Tube Formation by Thromboxane A2 J. Biol. Chem., December 10, 1999; 274(50): 35562 - 35570. [Abstract] [Full Text] [PDF] |
||||
![]() |
I. Mussini, D. Biral, O. Marin, S. Furlan, and S. Salvatori Myotonic Dystrophy Protein Kinase Expressed in Rat Cardiac Muscle Is Associated with Sarcoplasmic Reticulum and Gap Junctions J. Histochem. Cytochem., March 1, 1999; 47(3): 383 - 392. [Abstract] [Full Text] |
||||
|
Circulation Research Home | Subscriptions | Archives | Feedback | Authors | Help | AHA Journals Home | Search Copyright © 1998 American Heart Association, Inc. All rights reserved. Unauthorized use prohibited. |