MBNL1 Regulates Programmed Postnatal Switching Between Regenerative and Differentiated Cardiac States.
Logan R J BaileyDarrian BuggIsabella M ReichardtC Dessirée OrtaçAbigail NagleJagadambika GunajeAmy MartinsonRichard S JohnsonMichael J MacCossTomoya SakamotoDaniel P KellyMichael RegnierJennifer M DavisPublished in: Circulation (2024)
Here, MBNL1 was identified as an essential regulator of cardiomyocyte differentiated states, their developmental switch from hyperplastic to hypertrophic growth, and their regenerative potential through controlling an entire maturation program by stabilizing adult myocyte mRNAs during postnatal development and throughout adulthood. Targeting loss of cardiomyocyte maturity and downregulation of cell cycle inhibitors through MBNL1 deletion was not sufficient to promote adult regeneration.
Keyphrases
- cell cycle
- stem cells
- cell proliferation
- mesenchymal stem cells
- preterm infants
- cell therapy
- angiotensin ii
- tissue engineering
- left ventricular
- transcription factor
- depressive symptoms
- childhood cancer
- signaling pathway
- cancer therapy
- heart failure
- high glucose
- young adults
- atrial fibrillation
- drug delivery
- human health
- risk assessment
- endothelial cells
- early life
- genome wide analysis