Struzyna Laura A, Katiyar Kritika, Cullen D Kacy
Center for Brain Injury and Repair, Department of Neurosurgery, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States.
Philadelphia Veterans Affairs Medical Center, Philadelphia, PA, United States.
Curr Opin Solid State Mater Sci. 2014 Dec;18(6):308-318. doi: 10.1016/j.cossms.2014.07.004. Epub 2014 Sep 19.
Neural tissue engineers are exploiting key mechanisms responsible for neural cell migration and axonal path finding during embryonic development to create living scaffolds for neuroregeneration following injury and disease. These mechanisms involve the combined use of haptotactic, chemotactic, and mechanical cues to direct cell movement and re-growth. Living scaffolds provide these cues through the use of cells engineered in a predefined architecture, generally in combination with biomaterial strategies. Although several hurdles exist in the implementation of living regenerative scaffolds, there are considerable therapeutic advantages to using living cells in conjunction with biomaterials. The leading contemporary living scaffolds for neurorepair are utilizing aligned glial cells and neuronal/axonal tracts to direct regenerating axons across damaged tissue to appropriate targets, and in some cases to directly replace the function of lost cells. Future advances in technology, including the use of exogenous stimulation and genetically engineered stem cells, will further the potential of living scaffolds and drive a new era of personalized medicine for neuroregeneration.
神经组织工程师正在利用胚胎发育过程中负责神经细胞迁移和轴突路径寻找的关键机制,来创建用于损伤和疾病后神经再生的活体支架。这些机制涉及联合使用趋触性、趋化性和机械信号来引导细胞移动和再生。活体支架通过使用预先设计结构的细胞来提供这些信号,通常与生物材料策略相结合。尽管在实施活体再生支架方面存在一些障碍,但将活细胞与生物材料结合使用具有相当大的治疗优势。当代用于神经修复的主要活体支架正在利用排列的胶质细胞和神经元/轴突束,来引导再生轴突穿过受损组织到达合适的靶点,在某些情况下直接替代丢失细胞的功能。包括使用外源刺激和基因工程干细胞在内的未来技术进步,将进一步提升活体支架的潜力,并推动神经再生个性化医学的新时代。