Department of Chemical and Biomolecular Engineering, Yonsei University, 50 Yonsei-ro, Seodaemun-gu, Seoul 03722, Republic of Korea.
Department of Chemical and Biological Engineering, Gachon University, Seongnam-si, Gyeonggi-do 13120, Republic of Korea.
Mater Sci Eng C Mater Biol Appl. 2020 Oct;115:111128. doi: 10.1016/j.msec.2020.111128. Epub 2020 May 26.
Cell spheroid formation is necessary to develop three-dimensional (3D) cellular environments that provide appropriate cell-cell and cell-matrix interactions similar to in vivo environments without additional substrates. Although some methods including stirring culture, low adhesion plate culture, hanging drop, and microfluidics are used to construct cell spheroids, there is no method to fulfill all of the mass production of uniform spheroids, simple media change, and easy retrievability. Here, bulk poly(N-isopropylacrylamide) (PNIPAAm) hydrogel substrate (PHS) was used to fabricate, culture, and retrieve cell spheroids. Adipose-derived stem cells (ASCs) were cultured on bulk PHS to form spheroids. ASCs formed cell spheroids directly on substrates without additional manipulation. These spheroids adhered to the semi-adhesive substrate, while the spheroids fabricated using the nonadhesive surface method floated without getting fixed to the surface. Bulk PHS stiffness was evaluated using the compressive test (compressive modulus: 153 ± 11 kPa). A poly(ethylene glycol) (PEG) hydrogel microwell pattern was created on PHS to control the spheroid size, forming uniform ASC spheroids between 100 and 150 μm in diameter on 200 and 300 μm well-patterned substrates. Cell-cell interactions in the resulting ASC spheroids were evaluated based on fibronectin and laminin expression; fluorescence intensities of fibronectin- and laminin-immunostained images of ASC spheroids were 10.9 and 7.3 times higher than those of ASCs cultured on the tissue culture plate, respectively. ASC spheroids were detached following incubation at 4 °C for 10 min (retrieval efficiency: 74 ± 19%). Retrieved spheroid cell viability was over 97.5%. The PEG hydrogel microwell-patterned PHS is a convenient spheroid fabrication and retrieval platform that can increase cell spheroid usage.
细胞球状体的形成对于构建三维(3D)细胞环境是必要的,这种环境提供了类似于体内环境的适当细胞-细胞和细胞-基质相互作用,而无需额外的底物。尽管有一些方法,包括搅拌培养、低粘附板培养、悬滴和微流控,用于构建细胞球状体,但没有一种方法可以满足大规模生产均匀球状体、简单的介质更换和易于检索的要求。在这里,使用 bulk poly(N-isopropylacrylamide) (PNIPAAm) 水凝胶基底 (PHS) 来制造、培养和检索细胞球状体。脂肪来源的干细胞(ASCs)在 bulk PHS 上培养以形成球状体。ASCs 直接在基质上形成球状体,而使用非粘附表面方法制造的球状体则漂浮而不会固定在表面上。使用压缩试验评估 bulk PHS 的刚度(压缩模量:153 ± 11 kPa)。在 PHS 上创建聚(乙二醇)(PEG)水凝胶微井图案以控制球状体的大小,在 200 和 300 μm 图案化基底上形成直径在 100 至 150 μm 之间的均匀 ASC 球状体。基于纤连蛋白和层粘连蛋白的表达评估了所得 ASC 球状体中的细胞-细胞相互作用;ASC 球状体的纤连蛋白和层粘连蛋白免疫染色图像的荧光强度分别比在组织培养板上培养的 ASCs 高 10.9 和 7.3 倍。孵育 4°C 10 分钟后,ASC 球状体被分离(回收效率:74 ± 19%)。回收的球状体细胞活力超过 97.5%。PEG 水凝胶微井图案化 PHS 是一种方便的球状体制造和检索平台,可以增加细胞球状体的使用。