Laboratory for Biomedical Microsystems, Department of Biomedical Engineering, The Ohio State University, Columbus, Ohio, 43210, USA.
Department of Biological Chemistry and Pharmacology, The Ohio State University, Columbus, Ohio, 43210, USA.
Sci Rep. 2017 Aug 21;7(1):8361. doi: 10.1038/s41598-017-08723-2.
In tissue engineering, autofluorescence of polymer scaffolds often lowers the image contrast, making it difficult to examine cells and subcellular structures. Treating the scaffold materials with Sudan Black B (SBB) after cell fixation can effectively suppress autofluorescence, but this approach is not conducive to live cell imaging. Post-culture SBB treatment also disrupts intracellular structures and leads to reduced fluorescence intensity of the targets of interest. In this study, we introduce pre-culture SBB treatment to suppress autofluorescence, where SBB is applied to polymeric scaffold materials before cell seeding. The results show that the autofluorescence signals emitted from polycaprolactone (PCL) scaffolds in three commonly used fluorescence channels effectively decrease without diminishing the fluorescence signals emitted from the cells. The pre-culture SBB treatment does not significantly affect cell viability. The autofluorescence suppressive effect does not substantially diminish during the culturing period up to 28 days. The results also show that cell migration, proliferation, and myogenic differentiation in pre-culture SBB-treated groups do not exhibit statistical difference from the non-treated groups. As such, this approach greatly improves the fluorescence image quality for examining live cell behaviors and dynamics while the cells are cultured within autofluorescent polymer scaffolds.
在组织工程中,聚合物支架的自发荧光常常降低图像对比度,使得难以检查细胞和亚细胞结构。在细胞固定后用苏丹黑 B(SBB)处理支架材料可以有效地抑制自发荧光,但这种方法不利于活细胞成像。培养后的 SBB 处理也会破坏细胞内结构,并导致感兴趣的目标荧光强度降低。在这项研究中,我们介绍了预培养 SBB 处理来抑制自发荧光,其中 SBB 在细胞接种前应用于聚合物支架材料。结果表明,在三个常用的荧光通道中,从聚己内酯(PCL)支架发出的自发荧光信号有效地降低,而不会减弱细胞发出的荧光信号。预培养 SBB 处理对细胞活力没有显著影响。在长达 28 天的培养期间,自发荧光抑制效果没有明显减弱。结果还表明,与未经处理的组相比,预培养 SBB 处理组的细胞迁移、增殖和肌生成分化没有统计学差异。因此,这种方法极大地提高了荧光图像质量,可用于检查活细胞在具有自发荧光的聚合物支架内的行为和动态。