Chronic hemodynamic overload of the atria is an important factor for gap junction remodeling in human and rat hearts

• Published in: Cardiovascular research Vol. 72; no. 1; pp. 69 - 79
• Main Authors: RUCKER-MARTIN, Catherine, MILLIEZ, Paul, HATEM, Stéphane N, TAN, Sisareuth, DECROUY, Xavier, RECOUVREUR, Michel, VRANCKX, Roger, DELCAYRE, Claude, RENAUD, Jean-Francois, DUNIA, Irene, SEGRETAIN, Dominique
• Format: Journal Article
• Language: English
• Published: Oxford Oxford University Press 01.10.2006; Oxford University Press (OUP)
• Subjects: Animals; Atrial Fibrillation - metabolism; Atrial Fibrillation - pathology; Biological and medical sciences; Cardiac dysrhythmias; Cardiology. Vascular system; Cell Behavior; Cell Communication; Cellular Biology; Connexin 43 - analysis; Fibrosis; Freeze Fracturing; Gap Junctions - metabolism; Gap Junctions - pathology; Heart; Heart Atria - metabolism; Heart Atria - ultrastructure; Humans; Imaging, Three-Dimensional; Immunoblotting; Immunohistochemistry; Life Sciences; Medical sciences; Microscopy, Electron; Myocardial Infarction - metabolism; Myocardial Infarction - pathology; Rats; Heart; Atrial myocardium; Arrhythmia; Rat; Cardiovascular disease; Phlebology; Gap junction; Vascular remodeling; Connexin; Heart disease; Cardiology; Human; Atrial fibrillation; Rodentia; Excitability disorder; Vertebrata; Chronic; Mammalia; Overload; Animal; Fibrosis; Myocardium; Connexins; Circulatory system; Hemodynamics
• ISSN: 0008-6363; 1755-3245
• DOI: 10.1016/j.cardiores.2006.06.016

The expression and distribution of connexins is abnormal in a number of cardiac diseases, including atrial fibrillation, and is believed to favor conduction slowing and arrhythmia. Here, we studied the role of atrial structural remodeling in the disorganization of gap junctions and whether redistributed connexins can form new functional junction channels. Expression of connexin-43 (Cx43) was characterized by immunoblotting and immunohistochemistry in human right atrial specimens and in rat atria after myocardial infarction (MI). Gap junctions were studied by electron and 3-D microscopy, and myocyte-myocyte coupling was determined by Lucifer yellow dye transfer. In both chronically hemodynamically overloaded human atria in sinus rhythm and in dilated atria from MI-rats, Cx43 were dephosphorylated and redistributed from the intercalated disc to the lateral cell membranes as observed during atrial fibrillation. In MI-rats, the gap junctions at the intercalated disc were smaller (20% decrease) and contained very little Cx43 (0 or 1 gold particle vs. 42 to 98 in sham-operated rats). In the lateral membranes of myocytes, numerous connexon aggregates comprising non-phosphorylated Cx43 were observed. These connexon aggregates were in no case assembled into gap junction plaque-like structures. However, N-cadherin was well organized in the intercalated disc. There was very little myocyte-myocyte coupling in MI-rat atria and no myocyte-fibroblast coupling. Regression of the atrial remodeling was associated with the normalization of Cx43 localization. Structural alteration of the atrial myocardium is an important factor in the disorganization of connexins and gap junction. Moreover, redistributed Cx43 do not form junction channels.