State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, College of Materials Science and Engineering, Donghua University, Shanghai 201620, China.
Shanghai Engineering Research Center of Nano-Biomaterials and Regenerative Medicine, Donghua University, Shanghai 201620, China.
ACS Appl Mater Interfaces. 2023 Jul 19;15(28):33480-33490. doi: 10.1021/acsami.3c06627. Epub 2023 Jul 2.
Artificial cell spheroids are gaining importance in tissue engineering and regenerative medicine fields. Biomimetic construction of stem cell spheroids is nevertheless challenging, and bioplatforms permitting controllable and high-efficient fabrication of functional stem cell spheroids are needed. Here, a fractal nanofiber-based bioplatform is developed based on a tunable interfacial-induced crystallization approach, allowing a programmed culture of artificial stem cell spheroids under an ultralow cell seeding density. Specifically, starting with the nanofibers of poly(L-lactide) (PLLA) and gelatin (PG), an interfacial growth of PLLA nanocrystals is subsequently performed to construct the fractal nanofiber-based biotemplates (C-PG). Cell experiments with human dental pulp stem cells (hDPSCs) demonstrate that the fractal C-PG could effectively decrease cell-matrix interactions, thus facilitating spontaneous cell spheroid formation even under a low cell seeding density (1 × 10 cells/cm). Nanotopological properties of the C-PG bioplatform can be tuned by adjusting the fractal degree, thus enabling its suitability for the 3D culture of diverse hDPSC spheroids. Such a strategy provides a relatively simple and low-cost option for formation, expansion, and utility of stem cell spheroids. It offers another promising pathway to advance the development of stem cell therapies.
人工细胞球体在组织工程和再生医学领域越来越重要。然而,仿生构建干细胞球体具有挑战性,需要能够可控且高效地制造功能性干细胞球体的生物平台。在这里,我们基于可调界面诱导结晶方法开发了一种分形纳米纤维基生物平台,允许在超低细胞接种密度下对人工干细胞球体进行程序化培养。具体而言,从聚(L-乳酸)(PLLA)和明胶(PG)的纳米纤维开始,随后进行 PLLA 纳米晶的界面生长,以构建基于分形纳米纤维的生物模板(C-PG)。用人牙髓干细胞(hDPSCs)进行的细胞实验表明,分形 C-PG 可以有效降低细胞-基质相互作用,从而即使在低细胞接种密度(1×10 个细胞/cm)下也能促进自发的细胞球体形成。通过调整分形度可以调节 C-PG 生物平台的纳米拓扑性质,从而使其适用于各种 hDPSC 球体的 3D 培养。这种策略为干细胞球体的形成、扩增和应用提供了一种相对简单和低成本的选择。它为推进干细胞治疗的发展提供了另一种有前途的途径。