Unravelling the molecular activation of the reparative cardiac fibroblasts after myocardial infarction
Hernandez, S. C.; Ainciburu, M.; Sudupe, L.; Planell, N.; Vilas-Zornoza, A.; Lopez-Moreno, M.; Sarvide, S.; Diaz-Martinez, L.; Cobos-Figueroa, J.; San Martin-Uriz, P.; Muinos-Lopez, E.; Abizanda, G.; Ripalda-Cemborain, P.; Lagani, V.; Romero, J. P.; Tegner, J.; Perez-Pomares, J. M.; Wu, M.; Janssens, S.; Prosper, F.; Gomez-Cabrero, D.; Ruiz-Villalba, A.
Show abstract
Activated cardiac fibroblasts (Postn+ CFs) are responsible for the healing of the heart tissue after a myocardial infarction (MI). However, so far little is known about the moment that CFs are activated, and the genes involved in this process. This is especially relevant in the context of CF heterogeneity and their role in the response to the damage. In this context, we have described a subpopulation of activated CFs responsible for the healing scar and for preventing the rupture of the ventricle after the damage: the Reparative Cardiac Fibroblasts (RCFs). Our new data indicate that RCFs directly derived from activated CFs, and this transcriptional shift happens in a close window after damage. Interestingly, our results exhibited two different molecular dynamics that would give rise to this activation and, consequently, the appearance of definitive RCFs. Using bulk RNA-Seq, RNAScope and Spatial Transcriptomics, we anatomically localized some of the genes related to both dynamics in the infarcted heart and highlight the potential role of Aspn as a new marker of this transcriptional transition in mice, pigs and patients.
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