Laboratorio di Biologia dello Sviluppo, Dipartimento di Biologia e Biotecnologie 'Lazzaro Spallanzani', Università degli Studi di Pavia, Via Ferrata 9, 27100 Pavia, Italy.
Mutat Res. 2013 Aug 30;756(1-2):37-45. doi: 10.1016/j.mrgentox.2013.06.007. Epub 2013 Jun 20.
Embryonic stem cells (ESCs) for their derivation from the inner cell mass of a blastocyst represent a valuable in vitro model to investigate the effects of ionizing radiation on early embryonic cellular response. Following irradiation, both human and mouse ESCs (mESCs) maintain their pluripotent status and the capacity to differentiate into embryoid bodies and to form teratomas. Although informative of the maintenance of a pluripotent status, these studies never investigated the capability of irradiated ESCs to form specific differentiated phenotypes. Here, for the first time, 5Gy-irradiated mESCs were differentiated into cardiomyocytes, thus allowing the analysis of the long-term effects of ionizing radiations on the differentiation potential of a pluripotent stem cell population. On treated mESCs, 96h after irradiation, a genome-wide expression analysis was first performed in order to determine whether the treatment influenced gene expression of the surviving mESCs. Microarrays analysis showed that only 186 genes were differentially expressed in treated mESCs compared to control cells; a quarter of these genes were involved in cellular differentiation, with three main gene networks emerging, including cardiogenesis. Based on these results, we differentiated irradiated mESCs into cardiomyocytes. On day 5, 8 and 12 of differentiation, treated cells showed a significant alteration (qRT-PCR) of the expression of marker genes (Gata-4, Nkx-2.5, Tnnc1 and Alpk3) when compared to control cells. At day 15 of differentiation, although the organization of sarcomeric α-actinin and troponin T proteins appeared similar in cardiomyocytes differentiated from either mock or treated cells, the video evaluation of the kinematics and dynamics of the beating cardiac syncytium evidenced altered contractile properties of cardiomyocytes derived from irradiated mESCs. This alteration correlated with significant reduction of Connexin 43 foci. Our results indicate that mESCs populations that survive an ionizing irradiation treatment are capable to differentiate into cardiomyocytes, but they have altered contractile properties.
胚胎干细胞(ESCs)来源于囊胚的内细胞团,是研究电离辐射对早期胚胎细胞反应影响的宝贵体外模型。照射后,人和鼠的 ESCs(mESCs)均保持其多能状态和分化为胚状体并形成畸胎瘤的能力。尽管这些研究表明维持多能状态,但从未研究过照射后的 ESCs 形成特定分化表型的能力。在这里,首次将 5Gy 照射的 mESCs 分化为心肌细胞,从而允许分析电离辐射对多能干细胞群体分化潜力的长期影响。在处理后的 mESCs 中,在照射后 96 小时,首先进行全基因组表达分析,以确定处理是否影响存活的 mESCs 的基因表达。微阵列分析表明,与对照细胞相比,处理后的 mESCs 中仅有 186 个基因差异表达;其中四分之一的基因参与细胞分化,出现了三个主要的基因网络,包括心脏发生。基于这些结果,我们将照射后的 mESCs 分化为心肌细胞。在分化的第 5、8 和 12 天,与对照细胞相比,处理细胞的标记基因(Gata-4、Nkx-2.5、Tnnc1 和 Alpk3)的表达发生了显著改变(qRT-PCR)。在分化的第 15 天,尽管源自模拟或处理细胞的心肌细胞中肌球蛋白结合蛋白 Cα-肌动蛋白和肌钙蛋白 T 蛋白的组织相似,但对搏动心肌细胞同步性的运动学和动力学的视频评估表明,源自照射后的 mESCs 的心肌细胞的收缩特性发生改变。这种改变与连接蛋白 43 焦点的显著减少相关。我们的结果表明,在电离辐射处理后存活的 mESCs 群体能够分化为心肌细胞,但它们的收缩特性发生改变。