Department of Materials Science and Chemical Engineering, Stevens Institute of Technology, Hoboken, NJ, USA.
Department of Biomedical Engineering, Chemistry and Biological Sciences, Stevens Institute of Technology, Hoboken, NJ, USA.
Bone. 2017 Dec;105:245-252. doi: 10.1016/j.bone.2017.09.012. Epub 2017 Sep 21.
A human bone tissue model was developed by constructing ex vivo the 3D network of osteocytes via the biomimetic assembly of primary human osteoblastic cells with 20-25μm microbeads and subsequent microfluidic perfusion culture. The biomimetic assembly: (1) enabled 3D-constructed cells to form cellular network via processes with an average cell-to-cell distance of 20-25μm, and (2) inhibited cell proliferation within the interstitial confine between the microbeads while the confined cells produced extracellular matrix (ECM) to form a mechanically integrated structure. The mature osteocytic expressions of SOST and FGF23 genes became significantly higher, especially for SOST by 250 folds during 3D culture. The results validate that the bone tissue model: (1) consists of 3D cellular network of primary human osteocytes, (2) mitigates the osteoblastic differentiation and proliferation of primary osteoblast-like cells encountered in 2D culture, and (3) therefore reproduces ex vivo the phenotype of human 3D-networked osteocytes. The 3D tissue construction approach is expected to provide a clinically relevant and high-throughput means for evaluating drugs and treatments that target bone diseases with in vitro convenience.
构建了一个人骨组织模型,通过仿生组装原代人成骨细胞与 20-25μm 微珠,并随后进行微流控灌注培养,构建了体外 3D 骨细胞网络。仿生组装:(1)使 3D 构建的细胞通过平均细胞间距离为 20-25μm 的过程形成细胞网络;(2)在微珠之间的间隙限制细胞增殖,同时限制细胞产生细胞外基质 (ECM) 以形成机械整合结构。SOST 和 FGF23 基因的成熟成骨细胞表达显著增加,特别是在 3D 培养中 SOST 增加了 250 倍。结果验证了该骨组织模型:(1)由原代人成骨细胞的 3D 细胞网络组成;(2)减轻了 2D 培养中遇到的原代成骨样细胞的成骨分化和增殖;(3)因此,在体外再现了人 3D 网络骨细胞的表型。3D 组织构建方法有望为评估针对骨疾病的药物和治疗方法提供一种具有临床相关性和高通量的体外便利手段。