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Dev Biol ; 516: 130-137, 2024 Dec.
Article de Anglais | MEDLINE | ID: mdl-39127438

RÉSUMÉ

The functioning of the cardiovascular system is critical for embryo survival. Cardiac contractions depend on the sequential activation of different classes of voltage-gated ion channels. Understanding the fundamental features of these interactions is important for identifying the mechanisms of pathologies development in the myocardium. However, at present there is no consensus on which ion channels are involved in the formation of automaticity in the early embryonic stages. The aim of this study was to elucidate the expression of genes encoding various types of ion channels that are involved in the generation of electrical activity chicken heart at different stages of ontogenesis. We analyzed the expression of 14 genes from different families of ion channels. It was revealed that the expression profiles of ion channel genes change depending on the stages of ontogenesis. The HCN4, CACNA1D, SCN1A, SCN5A, KCNA1 genes have maximum expression at the tubular heart stage. In adult, a switch occurs to the higher expression of CACNA1C, KCNH6, RYR and SLC8A1 genes. This data correlated with the results obtained by the microelectrode method. It can be assumed that the automaticity of the tubular heart is mainly due to the mechanism of the «membrane-clock¼ (hyperpolarization-activated current (If), Ca2+-current L-type (ICaL), Na+-current (INa) and the slow component of the delayed rectifier K+-current (IKs)). Whereas in adult birds, the mechanism for generating electrical impulses is determined by both « membrane- clock¼ and «Ca2+-clock¼.


Sujet(s)
Poulets , Régulation de l'expression des gènes au cours du développement , Coeur , Myocarde , Animaux , Embryon de poulet , Myocarde/métabolisme , Poulets/génétique , Coeur/embryologie , Canal de libération du calcium du récepteur à la ryanodine/génétique , Canal de libération du calcium du récepteur à la ryanodine/métabolisme , Échangeur sodium-calcium/génétique , Échangeur sodium-calcium/métabolisme , Canaux contrôlés par les nucléotides cycliques et activés par l'hyperpolarisation/génétique , Canaux contrôlés par les nucléotides cycliques et activés par l'hyperpolarisation/métabolisme , Canaux ioniques/génétique , Canaux ioniques/métabolisme
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