Vuorenpää Hanna, Valtonen Joona, Penttinen Kirsi, Koskimäki Sanna, Hovinen Emma, Ahola Antti, Gering Christine, Parraga Jenny, Kelloniemi Minna, Hyttinen Jari, Kellomäki Minna, Aalto-Setälä Katriina, Miettinen Susanna, Pekkanen-Mattila Mari
Adult Stem Cell Group, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.
Tays Research Services, Wellbeing Services County of Pirkanmaa, Tampere University Hospital, Tampere, Finland.
Cytotechnology. 2024 Aug;76(4):483-502. doi: 10.1007/s10616-024-00630-5. Epub 2024 May 2.
Cardiovascular diseases remain as the most common cause of death worldwide. To reveal the underlying mechanisms in varying cardiovascular diseases, in vitro models with cells and supportive biomaterial can be designed to recapitulate the essential components of human heart. In this study, we analyzed whether 3D co-culture of cardiomyocytes (CM) with vascular network and with adipose tissue-derived mesenchymal stem/stromal cells (ASC) can support CM functionality. CM were cultured with either endothelial cells (EC) and ASC or with only ASC in hydrazide-modified gelatin and oxidized gellan gum hybrid hydrogel to form cardiovascular multiculture and myocardial co-culture, respectively. We studied functional characteristics of CM in two different cellular set-ups and analyzed vascular network formation, cellular morphology and orientation. The results showed that gellan gum-gelatin hydrogel supports formation of two different cellular networks and functional CM. We detected formation of a modest vascular network in cardiovascular multiculture and extensive ASC-derived alpha smooth muscle actin -positive cellular network in multi- and co-culture. iPSC-CM showed elongated morphology, partly aligned orientation with the formed networks and presented normal calcium transients, beating rates, and contraction and relaxation behavior in both setups. These 3D cardiac models provide promising platforms to study (patho) physiological mechanisms of cardiovascular diseases.
The online version contains supplementary material available at 10.1007/s10616-024-00630-5.
心血管疾病仍然是全球最常见的死亡原因。为了揭示不同心血管疾病的潜在机制,可以设计包含细胞和支持性生物材料的体外模型来重现人类心脏的基本组成部分。在本研究中,我们分析了心肌细胞(CM)与血管网络以及脂肪组织来源的间充质干/基质细胞(ASC)的三维共培养是否能支持CM的功能。将CM分别与内皮细胞(EC)和ASC或仅与ASC在酰肼修饰的明胶和氧化结冷胶混合水凝胶中培养,以分别形成心血管多细胞培养和心肌共培养。我们研究了两种不同细胞组合中CM的功能特性,并分析了血管网络形成、细胞形态和取向。结果表明,结冷胶-明胶水凝胶支持两种不同细胞网络和功能性CM的形成。我们在心血管多细胞培养中检测到适度的血管网络形成,在多细胞培养和共培养中检测到广泛的ASC来源的α平滑肌肌动蛋白阳性细胞网络。诱导多能干细胞衍生的CM在两种组合中均呈现细长形态,部分与形成的网络对齐,并表现出正常的钙瞬变、搏动率以及收缩和舒张行为。这些三维心脏模型为研究心血管疾病的(病理)生理机制提供了有前景的平台。
在线版本包含可在10.1007/s10616-024-00630-5获取的补充材料。