PHEniX Laboratory, Department of Pulmonary Medicine, Amsterdam UMC Location Vrije Universiteit Amsterdam, De Boelelaan 1117, Amsterdam, The Netherlands.
Amsterdam Cardiovascular Sciences, Pulmonary Hypertension and Thrombosis, Amsterdam, The Netherlands.
Sci Rep. 2024 Apr 29;14(1):9795. doi: 10.1038/s41598-024-60102-w.
Cardiac fibrosis contributes to the development of heart failure, and is the response of cardiac fibroblasts (CFs) to pressure or volume overload. Limiting factors in CFs research are the poor availability of human cells and the tendency of CFs to transdifferentiate into myofibroblasts when cultured in vitro. The possibility to generate CFs from induced pluripotent stem cells (iPSC), providing a nearly unlimited cell source, opens new possibilities. However, the behaviour of iPSC-CFs under mechanical stimulation has not been studied yet. Our study aimed to assess the behaviour of iPSC-CFs under mechanical stretch and pro-fibrotic conditions. First, we confirm that iPSC-CFs are comparable to primary CFs at gene, protein and functional level. Furthermore, iPSC-derived CFs adopt a pro-fibrotic response to transforming growth factor beta (TGF-β). In addition, mechanical stretch inhibits TGF-β-induced fibroblast activation in iPSC-CFs. Thus, the responsiveness to cytokines and mechanical stimulation of iPSC-CFs demonstrates they possess key characteristics of primary CFs and may be useful for disease modelling.
心肌纤维化是心力衰竭发展的原因,也是心脏成纤维细胞(CFs)对压力或容量超负荷的反应。CFs 研究的限制因素是人类细胞的可用性差,以及 CFs 在体外培养时容易向肌成纤维细胞转分化。从诱导多能干细胞(iPSC)中生成 CFs,提供了几乎无限的细胞来源,这为研究带来了新的可能性。然而,iPSC-CFs 在机械刺激下的行为尚未得到研究。我们的研究旨在评估 iPSC-CFs 在机械拉伸和促纤维化条件下的行为。首先,我们证实 iPSC-CFs 在基因、蛋白和功能水平上与原代 CFs 相当。此外,iPSC 衍生的 CFs 对转化生长因子-β(TGF-β)产生促纤维化反应。此外,机械拉伸抑制了 iPSC-CFs 中 TGF-β 诱导的成纤维细胞激活。因此,iPSC-CFs 对细胞因子和机械刺激的反应表明它们具有原代 CFs 的关键特征,可能有助于疾病建模。