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, Après avoir sélectionné et caractérisé une population de cellules souches d'origine mésenchymateuse, isolée à partir d'auricules humaines, exprimant le marqueur W8B2 (CSCs W8B2+), nous nous sommes focalisés (par les techniques de RT-qPCR à haut rendement, d'immuno-marquage, de western-blot et de fluorescence calcique) sur
, Les résultats montrent que CSCs W8B2+ tendent à se différencier en cellules pacemaker
, expriment durant la différenciation. L'enregistrement de l'activité calcique (via une sonde optogénétique) montre la présence d'oscillations calciques qui évoluent en fréquence et en intensité pendant la différenciation. Les stocks-IP3 sensibles et l'échangeur NCX
, Nous avons ensuite étudié l'importance du canal BKCa et des récepteurs sphingosine 1phosphate (S1P) dans la régulation des propriétés fondamentales des CSCs W8B2+
, L'inhibition du BKCa diminue la prolifération cellulaire en accumulant les cellules à la phase G0/G1, réprime l'auto-renouvellement mais n'affecte pas la migration
, Mots-clés : thérapie cellulaire, cellules souches cardiaques humaines, cellules mésenchymateuses, différenciation, canaux ioniques, signalisation calcique, canal BKCa, sphingosine 1-phosphate, optogénétique