Guo Yonglong, Liu Qing, Yang Yan, Guo Xiaoling, Lian Ruiling, Li Shanyi, Wang Chan, Zhang Shiqi, Chen Jiansu
1 Key Laboratory for Regenerative Medicine of Ministry of Education, Jinan University , Guangzhou, 510632, China .
Cell Reprogram. 2015 Feb;17(1):77-87. doi: 10.1089/cell.2014.0070. Epub 2014 Dec 30.
The spheroids of 3-dimensional culture and Rho-associated kinase (ROCK) inhibitor Y-27632 have shown many advantages for the promotion of cellular viability and proliferation. The objective of this study was to investigate the effect of Y-27632 on the growth and injectability of bovine corneal endothelial cells (B-CECs) maintained in vitro as spheroid cultures. Immunofluorescence staining showed that Y-27632 did not alter the cell type specificity of B-CECs, but it significantly enhanced B-CEC spherical viability and proliferation by a Live/Dead assay, 5-ethynyl-2'-deoxyuridine (EdU) labeling assay, and Cell Counting Kit-8 (CCK-8) assay. The uniform B-CEC spheroids could easily form in multiwall agarose micromolds and had a higher stemness potential than single B-CECs. Injectable B-CEC spheroids were able to form monolayer growth, and polygonal B-CECs completely covered culture plates or Descemet's membrane of decellularized corneas under inverted microscopy and scanning electron microscopy (SEM). B-CEC spheroids were generated from agarose microwells on day 1 and then adherent culture with Y-27632 for day 5. However, small B-CEC spheroids still existed on culture plates or decellularized corneas when B-CEC spheroids were cultured in the same condition except for absence of Y-27632. Our findings that CEC spheroids with Y-27632 are injectable in vitro have important implications for the favorable treatment of CEC deficiency.
三维培养的球体和Rho相关激酶(ROCK)抑制剂Y-27632在促进细胞活力和增殖方面显示出许多优势。本研究的目的是探讨Y-27632对体外维持为球体培养的牛角膜内皮细胞(B-CEC)生长和可注射性的影响。免疫荧光染色显示,Y-27632并未改变B-CEC的细胞类型特异性,但通过活/死检测、5-乙炔基-2'-脱氧尿苷(EdU)标记检测和细胞计数试剂盒-8(CCK-8)检测,它显著增强了B-CEC球体的活力和增殖。均匀的B-CEC球体能够在多壁琼脂糖微模具中轻松形成,并且比单个B-CEC具有更高的干性潜能。可注射的B-CEC球体能够形成单层生长,并且在倒置显微镜和扫描电子显微镜(SEM)下,多边形的B-CEC完全覆盖培养板或脱细胞角膜的Descemet膜。B-CEC球体在第1天从琼脂糖微孔中生成,然后在第5天用Y-27632进行贴壁培养。然而,当B-CEC球体在除无Y-27632外的相同条件下培养时,培养板或脱细胞角膜上仍存在小的B-CEC球体。我们的研究结果表明,含有Y-27632的CEC球体在体外具有可注射性,这对CEC缺乏症的良好治疗具有重要意义。