Publication
Lack of the transcription factor Nfix causes tachycardia in mice sinus node and rats neonatal cardiomyocytes
Publisher:
Wiley
Date:
14-05-2023
DOI:
10.1111/APHA.13981
Abstract: Nfix is a transcription factor belonging to the Nuclear Factor I (NFI) family comprising four members ( Nfia , b , c , x ). Nfix plays important roles in the development and function of several organs. In muscle development , Nfix controls the switch from embryonic to fetal myogenesis by promoting fast twitching fibres. In the adult muscle, following injury, lack of Nfix impairs regeneration, inducing higher content of slow‐twitching fibres. Nfix is expressed also in the heart, but its function has been never investigated before. We studied Nfix role in this organ. Using Nfix ‐null and wild type (WT) mice we analyzed: (1) the expression pattern of Nfix during development by qPCR and (2) the functional alterations caused by its absence, by in vivo telemetry and in vitro patch cl analysis. Nfix expression start in the heart from E12.5. Adult hearts of Nfix ‐null mice show a hearts morphology and sarcomeric proteins expression similar to WT. However, Nfix ‐null animals show tachycardia that derives form an intrinsic higher beating rate of the sinus node (SAN). Molecular and functional analysis revealed that sinoatrial cells of Nfix ‐null mice express a significantly larger L‐type calcium current ( Cacna1d + Cacna1c ). Interestingly, downregulation of Nfix by sh‐RNA in primary cultures of neonatal rat ventricular cardiomyocytes induced a similar increase in their spontaneous beating rate and in I CaL current. In conclusion, our data provide the first demonstration of a role of Nfix that, increasing the L‐type calcium current, modulates heart rate.