Paracrine effect of regulatory T cells promotes cardiomyocyte proliferation during pregnancy and after myocardial infarction.
Serena ZacchignaValentina MartinelliSilvia MoimasAndrea CollivaMarco AnziniAndrea NordioAlessia CostaMichael RehmanSimone VodretCristina PierroGiulia ColussiLorena ZentilinMaria Ines GutierrezEllen DirkxCarlin LongGianfranco SinagraDavid KlatzmannMauro GiaccaPublished in: Nature communications (2018)
Cardiomyocyte proliferation stops at birth when the heart is no longer exposed to maternal blood and, likewise, to regulatory T cells (Tregs) that are expanded to promote maternal tolerance towards the fetus. Here, we report a role of Tregs in promoting cardiomyocyte proliferation. Treg-conditioned medium promotes cardiomyocyte proliferation, similar to the serum from pregnant animals. Proliferative cardiomyocytes are detected in the heart of pregnant mothers, and Treg depletion during pregnancy decreases both maternal and fetal cardiomyocyte proliferation. Treg depletion after myocardial infarction results in depressed cardiac function, massive inflammation, and scarce collagen deposition. In contrast, Treg injection reduces infarct size, preserves contractility, and increases the number of proliferating cardiomyocytes. The overexpression of six factors secreted by Tregs (Cst7, Tnfsf11, Il33, Fgl2, Matn2, and Igf2) reproduces the therapeutic effect. In conclusion, Tregs promote fetal and maternal cardiomyocyte proliferation in a paracrine manner and improve the outcome of myocardial infarction.
Keyphrases
- regulatory t cells
- signaling pathway
- angiotensin ii
- high glucose
- pregnancy outcomes
- dendritic cells
- pregnant women
- oxidative stress
- endothelial cells
- atrial fibrillation
- pi k akt
- cell proliferation
- immune response
- acute coronary syndrome
- acute myocardial infarction
- smooth muscle
- preterm birth
- weight loss
- tissue engineering
- binding protein