Regenerative and Restorative Medicine Research Center (REMER), Research Institute for Health Sciences and Technologies (SABITA), Istanbul Medipol University, Istanbul, Turkey.
Medical Microbiology Graduate Program, Health Sciences Institute, Istanbul Medipol University, Istanbul, Turkey.
Methods Mol Biol. 2022;2520:161-170. doi: 10.1007/7651_2021_450.
Human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CM) create an unlimited cell source for basic and translational cardiac research. Obtaining hiPSC-CM culture as a single-cell, monolayer or three-dimensional clusters for downstream applications can be challenging. Thus, it is critical to develop replating strategies for hiPSC-CMs by evaluating different enzymatic or nonenzymatic reagents for dissociation and seeding on different coating materials. To reseed hiPSC-CMs with high viability and at structures desirable for the downstream applications, here we defined optimized protocols to dissociate hiPSC-CMs by using collagenase A&B, Collagenase II, TrypLE, and EDTA and reseeding on various matrix materials including fibronectin, laminin, imatrix, Matrigel, and Geltrex. By the replating methods described here, a single cell or cluster-containing hiPSC-CM cultures can be generated effectively.
人诱导多能干细胞衍生的心肌细胞(hiPSC-CM)为基础和转化心脏研究提供了无限的细胞来源。获得单细胞、单层或三维簇的 hiPSC-CM 培养物用于下游应用可能具有挑战性。因此,通过评估不同的酶或非酶试剂用于解离和在不同的涂层材料上播种,开发 hiPSC-CM 的重铺策略至关重要。为了以高活力和适合下游应用的结构重新播种 hiPSC-CM,我们在这里定义了优化的方案,通过使用胶原酶 A&B、胶原酶 II、TrypLE 和 EDTA 进行 hiPSC-CM 的解离,并在各种基质材料上重新播种,包括纤连蛋白、层粘连蛋白、imatrix、Matrigel 和 Geltrex。通过这里描述的重铺方法,可以有效地生成含有单个细胞或细胞簇的 hiPSC-CM 培养物。