Department of Materials Science and Engineering and ⊥Davis Heart and Lung Research Institute, The Ohio State University , Columbus, Ohio 43210, United States.
Department of Gerontology, Tongji Hospital, and ∥Tongji Hospital, Tongji University , Shanghai, China.
ACS Appl Mater Interfaces. 2016 Jun 29;8(25):15948-57. doi: 10.1021/acsami.6b04932. Epub 2016 Jun 20.
Cardiac stem cell therapy has been considered as a promising strategy for heart tissue regeneration. Yet achieving cardiac differentiation after stem cell transplantation remains challenging. This compromises the efficacy of current stem cell therapy. Delivery of cells using matrices that stimulate the cardiac differentiation may improve the degree of cardiac differentiation in the heart tissue. In this report, we investigated whether elastic modulus of highly flexible poly(N-isopropylamide) (PNIPAAm)-based hydrogels can be modulated to stimulate the encapsulated cardiosphere derived cells (CDCs) to differentiate into cardiac lineage under static condition and dynamic stretching that mimics the heart beating condition. We have developed hydrogels whose moduli do not change under both dynamic stretching and static conditions for 14 days. The hydrogels had the same chemical structure but different elastic moduli (11, 21, and 40 kPa). CDCs were encapsulated into these hydrogels and cultured under either native heart-mimicking dynamic stretching environment (12% strain and 1 Hz frequency) or static culture condition. CDCs were able to grow in all three hydrogels. The greatest growth was found in the hydrogel with elastic modulus of 40 kPa. The dynamic stretching condition stimulated CDC growth. The CDCs demonstrated elastic modulus-dependent cardiac differentiation under both static and dynamic stretching conditions as evidenced by gene and protein expressions of cardiac markers such as MYH6, CACNA1c, cTnI, and Connexin 43. The highest differentiation was found in the 40 kPa hydrogel. These results suggest that delivery of CDCs with the 40 kPa hydrogel may enhance cardiac differentiation in the infarct hearts.
心脏干细胞治疗被认为是心肌组织再生的一种有前途的策略。然而,干细胞移植后实现心脏分化仍然具有挑战性。这会影响当前干细胞治疗的效果。使用基质来输送细胞,刺激心脏分化,可能会提高心脏组织中心脏分化的程度。在本报告中,我们研究了高度灵活的聚(N-异丙基丙烯酰胺)(PNIPAAm)基水凝胶的弹性模量是否可以调节,以刺激包封的心脏球源性细胞(CDCs)在静态条件和模拟心脏跳动条件的动态拉伸下分化为心脏谱系。我们开发了水凝胶,其在 14 天内的动态拉伸和静态条件下的模量都不会发生变化。这些水凝胶具有相同的化学结构,但弹性模量不同(11、21 和 40 kPa)。将 CDCs 包封在这些水凝胶中,并在模拟心脏的动态拉伸环境(12%应变和 1 Hz 频率)或静态培养条件下培养。CDCs 能够在这三种水凝胶中生长。在弹性模量为 40 kPa 的水凝胶中发现了最大的生长。动态拉伸条件刺激了 CDC 的生长。CDCs 在静态和动态拉伸条件下表现出弹性模量依赖性的心脏分化,这表现为心脏标志物如 MYH6、CACNA1c、cTnI 和 Connexin 43 的基因和蛋白表达。在 40 kPa 水凝胶中发现了最高的分化。这些结果表明,用 40 kPa 水凝胶输送 CDCs 可能会增强梗死心脏中的心脏分化。