Division of Biomaterials and Biomechanics, Department of Restorative Dentistry, School of Dentistry, Oregon Health and Science University, Portland, OR, 97201, USA.
Department of Biomedical Engineering, School of Medicine, Oregon Health and Science University, Portland, OR, 97239, USA.
Nat Commun. 2019 Aug 6;10(1):3520. doi: 10.1038/s41467-019-11455-8.
Bone tissue, by definition, is an organic-inorganic nanocomposite, where metabolically active cells are embedded within a matrix that is heavily calcified on the nanoscale. Currently, there are no strategies that replicate these definitive characteristics of bone tissue. Here we describe a biomimetic approach where a supersaturated calcium and phosphate medium is used in combination with a non-collagenous protein analog to direct the deposition of nanoscale apatite, both in the intra- and extrafibrillar spaces of collagen embedded with osteoprogenitor, vascular, and neural cells. This process enables engineering of bone models replicating the key hallmarks of the bone cellular and extracellular microenvironment, including its protein-guided biomineralization, nanostructure, vasculature, innervation, inherent osteoinductive properties (without exogenous supplements), and cell-homing effects on bone-targeting diseases, such as prostate cancer. Ultimately, this approach enables fabrication of bone-like tissue models with high levels of biomimicry that may have broad implications for disease modeling, drug discovery, and regenerative engineering.
骨组织从定义上讲是一种有机-无机纳米复合材料,其中代谢活跃的细胞嵌入在基质中,该基质在纳米尺度上严重钙化。目前,还没有能够复制这些骨组织明确特征的策略。在这里,我们描述了一种仿生方法,即在超饱和的钙和磷酸盐介质中加入非胶原蛋白类似物,以引导纳米级磷灰石在嵌入成骨细胞、血管和神经细胞的胶原的原纤维内和原纤维间空间的沉积。这个过程使我们能够工程设计出模拟骨细胞和细胞外微环境关键特征的骨模型,包括其蛋白引导的生物矿化、纳米结构、脉管系统、神经支配、固有成骨诱导特性(无需外源性补充),以及针对骨靶向疾病(如前列腺癌)的归巢效应。最终,这种方法能够制造出具有高度仿生特性的类骨组织模型,这可能对疾病建模、药物发现和再生工程具有广泛的意义。