The American journal of pathology · 1997
Dedifferentiation of atrial cardiomyocytes as a result of chronic atrial fibrillation.
СтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод пока не подготовлен
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Ausma J, Wijffels M, van Eys G, Koide M, Ramaekers F, Allessie M, Borgers M
Аннотация
Chronic atrial fibrillation was induced in goats by electrical pacing. After 9 to 23 weeks of sustained atrial fibrillation, the morphology of the atrial structures was examined. The majority of the cardiomyocytes exhibited marked changes in their cellular substructures, with the replacement of sarcomeres by glycogen as the main characteristic. Using immuno-histochemical staining procedures, we assessed the expression and organization of contractile and cytoskeletal proteins in these cases and compared them with the expression and organization of these proteins in normal atria. Part of the atrial cardiomyocytes acquired a dedifferentiated phenotype, as deduced from the re-expression of alpha-smooth muscle actin, the disappearance of cardiotin, and the staining patterns of titin, which resembled those of embryonic cardiomyocytes. From these results we conclude that chronic atrial fibrillation induces myocardial dedifferentiation. This model of chronic atrial fibrillation in goats offers the possibility to study the time course of changes in cardiac structure during sustained atrial fibrillation and after cardioversion.
Предметные рубрики MeSH
AnimalsAtrial FibrillationBiomarkersCardiac Pacing, ArtificialCell Adhesion MoleculesCell DifferentiationCell NucleusChronic DiseaseConnectinContractile ProteinsCytoskeletal ProteinsFemaleGoatsHeart AtriaImmunohistochemistryMuscle ProteinsMuscle, SmoothMyocardiumProtein KinasesSarcoplasmic Reticulum