Engineering spheroids potentiating cell-cell and cell-ECM interactions by self-assembly of stem cell microlayer

• Published in: Biomaterials 2018-05, Vol.165, p.105-120
• Main Authors: Lee, Yu Bin, Kim, Eun Mi, Byun, Hayeon, Chang, Hyung-kwan, Jeong, Kwanghee, Aman, Zachary M., Choi, Yu Suk, Park, Jungyul, Shin, Heungsoo
• Format: Article
• Language: English
• Subjects: Cell Communication; Extracellular Matrix; Humans; Hydrogels - chemistry; Mesenchymal Stem Cells - cytology; Micropatterning; Polydopamine; Regenerative Medicine; Spheroid; Spheroids, Cellular; Stem cell niche; Thermo-responsive hydrogel; Tissue Engineering
• ISSN: 0142-9612; 1878-5905
• DOI: 10.1016/j.biomaterials.2018.02.049

Numerous methods have been reported for the fabrication of 3D multi-cellular spheroids and their use in stem cell culture. Current methods typically relying on the self-assembly of trypsinized, suspended stem cells, however, show limitations with respect to cell viability, throughput, and accurate recapitulation of the natural microenvironment. In this study, we developed a new system for engineering cell spheroids by self-assembly of micro-scale monolayer of stem cells. We prepared synthetic hydrogels with the surface of chemically formed micropatterns (squares/circles with width/diameter of 200 μm) on which mesenchymal stem cells isolated from human nasal turbinate tissue (hTMSCs) were selectively attached and formed a monolayer. The hydrogel is capable of thermally controlled expansion. As the temperature was decreased from 37 to 4 °C, the cell layer detached rapidly (90%). Spheroidization was significantly delayed and occurred with reduced efficiency on circle patterns compared to square patterns. Multi-physics mapping supported that delamination of the micro-scale monolayer may be affected by stress concentrated at the corners of the square pattern. In contrast, stress was distributed symmetrically along the boundary of the circle pattern. In addition, treatment of the micro-scale monolayer with a ROCK inhibitor significantly retarded spheroidization, highlighting the importance of contraction mediated by actin stress fibers for the stable generation of spheroidal stem cell structures. Spheroids prepared from the assembly of monolayers showed higher expression, both on the mRNA and protein levels, of ECM proteins (fibronectin and laminin) and stemness markers (Oct4, Sox2, and Nanog) compared to spheroids prepared from low-attachment plates, in which trypsinized single cells are assembled. The hTMSC spheroids also presented enhanced expression levels of markers related to tri-lineage (osteogenic, chondrogenic and adipogenic) differentiation. The changes in microcellular environments and functionalities were double-confirmed by using adipose derived mesenchymal stem cells (ADSCs). This spheroid engineering technique may have versatile applications in regenerative medicine for functionally improved 3D culture and therapeutic cell delivery.