LIAN-CONICET, FLENI - Ruta 9 Km 52.5, Belén de Escobar, Buenos Aires, Argentina.
Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Ciudad Autónoma de Buenos Aires, Argentina.
J Cardiovasc Transl Res. 2018 Feb;11(1):1-13. doi: 10.1007/s12265-017-9769-6. Epub 2017 Oct 10.
Leukemia inhibitory factor (LIF) is a growth factor with pleiotropic biological functions. It has been reported that LIF acts at different stages during mesoderm development. Also, it has been shown that LIF has a cytoprotective effect on neonatal murine cardiomyocytes (CMs) in culture, but little is known about the role of LIF during human cardiogenesis. Thus, we analyzed the effects of LIF on human pluripotent stem cells (PSC) undergoing cardiac differentiation. We first showed that LIF is expressed in the human heart during early development. We found that the addition of LIF within a precise time window during the in vitro differentiation process significantly increased CMs viability. This finding was associated to a decrease in the expression of pro-apoptotic protein Bax, which coincides with a reduction of the apoptotic rate. Therefore, the addition of LIF may represent a promising strategy for increasing CMs survival derived from PSCs.
白血病抑制因子(LIF)是一种具有多种生物学功能的生长因子。据报道,LIF 在中胚层发育的不同阶段发挥作用。此外,已经表明 LIF 对培养中的新生鼠心肌细胞(CM)具有细胞保护作用,但对于 LIF 在人类心脏发生过程中的作用知之甚少。因此,我们分析了 LIF 对正在进行心脏分化的人类多能干细胞(PSC)的影响。我们首先表明,LIF 在人类心脏的早期发育过程中表达。我们发现,在体外分化过程中精确时间窗口内添加 LIF 可显著提高 CM 的活力。这一发现与促凋亡蛋白 Bax 的表达减少有关,凋亡率也随之降低。因此,添加 LIF 可能代表了一种增加源自 PSC 的 CM 存活率的有前途的策略。