Fischell Department of Bioengineering, University of Maryland, College Park, MD, 20742, USA.
Marlene and Stewart Greenebaum Comprehensive Cancer Center, University of Maryland, Baltimore, MD, 21201, USA.
Small. 2021 Aug;17(33):e2102219. doi: 10.1002/smll.202102219. Epub 2021 Jul 14.
Human induced pluripotent stem cells (iPSCs) are ideal for developing personalized medicine. However, the spontaneous differentiation of human iPSCs under conventional 2D and 3D cultures results in significant heterogeneity and compromised quality. Therefore, a method for effectively isolating and expanding high-quality human iPSCs is critically needed. Here, a biomimetic microencapsulation approach for isolating and culturing high-quality human iPSCs is reported. This is inspired by the natural proliferation and development of blastomeres into early blastocyst where the early embryonic stem cells-containing core is enclosed in a semipermeable hydrogel shell known as the zona pellucida (Zona). Blastomere cluster-like human iPSC clusters are encapsulated in a miniaturized (≈10 nanoliter) hyaluronic acid (HA)-rich core of microcapsules with a semipermeable Zona-like hydrogel shell and subsequently cultured to form pluripotent human iPSC spheroids with significantly improved quality. This is indicated by their high expression of pluripotency markers and highly efficient 3D cardiac differentiation. In particular, HA is found to be crucial for isolating the high-quality human iPSCs with the biomimetic core-shell microencapsulation culture. Interestingly, the isolated human iPSCs can maintain high pluripotency even after being cultured again in 2D. These discoveries and the bioinspired culture method may be valuable to facilitate the human iPSC-based personalized medicine.
人诱导多能干细胞(iPSCs)非常适合开发个性化药物。然而,在传统的 2D 和 3D 培养下,人 iPSCs 的自发分化会导致显著的异质性和质量受损。因此,迫切需要一种有效的方法来分离和扩增高质量的人 iPSCs。在这里,我们报道了一种仿生微囊化方法,用于分离和培养高质量的人 iPSCs。这是受早期囊胚中卵裂球的自然增殖和发育的启发,其中含有早期胚胎干细胞的核心被包裹在称为透明带(Zona)的半透性水凝胶壳中。类卵裂球簇的人 iPSC 簇被包裹在微型(≈10 纳升)富含透明质酸(HA)的微胶囊的核心中,具有半透性的 Zona 样水凝胶壳,随后进行培养以形成具有显著改善质量的多能性人 iPSC 球体。这可以通过其高水平的多能性标志物表达和高效的 3D 心脏分化来证明。特别是,发现 HA 对于使用仿生核壳微囊化培养分离高质量的人 iPSCs 至关重要。有趣的是,即使在再次进行 2D 培养后,分离的人 iPSCs 也能保持高多能性。这些发现和仿生培养方法可能有助于促进基于人 iPSC 的个性化药物的发展。