Department of Biomedical Engineering, Washington University, One Brookings Drive, St Louis, MO 63130, USA.
Biomaterials. 2010 Nov;31(33):8651-8. doi: 10.1016/j.biomaterials.2010.07.089. Epub 2010 Aug 19.
Visualizing cells in three-dimensional (3D) scaffolds has been one of the major challenges in tissue engineering. Most current imaging modalities either suffer from poor penetration depth or require exogenous contrast agents. Here, we demonstrate photoacoustic microscopy (PAM) of the spatial distribution and temporal proliferation of cells inside three-dimensional porous scaffolds with thicknesses over 1 mm. Specifically, we evaluated the effects of seeding and culture methods on the spatial distribution of melanoma cells. Spatial distribution of the cells in the scaffold was well-resolved in PAM images. Moreover, the number of cells in the scaffold was quantitatively measured from the as-obtained volumetric information. The cell proliferation profile obtained from PAM correlated well with what was obtained using the traditional 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay.
在三维(3D)支架中可视化细胞一直是组织工程中的主要挑战之一。目前大多数成像方式要么穿透深度不佳,要么需要外源性对比剂。在这里,我们展示了具有超过 1 毫米厚度的三维多孔支架内细胞的空间分布和时间增殖的光声显微镜(PAM)。具体而言,我们评估了接种和培养方法对黑色素瘤细胞空间分布的影响。在 PAM 图像中可以很好地分辨出支架中细胞的空间分布。此外,还可以从获得的体积信息中定量测量支架中的细胞数量。从 PAM 获得的细胞增殖曲线与使用传统的 3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴化物(MTT)测定法获得的结果非常吻合。