Farrag Mahmoud, Leipzig Nic D
Integrated Bioscience Program, The University of Akron, Akron, OH 44325, USA.
Department of Chemical and Biomolecular Engineering, The University of Akron, Akron, OH 44325, USA.
Cells. 2018 Oct 17;7(10):173. doi: 10.3390/cells7100173.
A combinatorial approach integrating stem cells and capable of exploiting available cues is likely needed to regenerate lost neural tissues and ultimately restore neurologic functions. This study investigates the effects of the subcutaneous maturation of adult-derived neural stem cell (aNSCs) seeded into biomaterial constructs on aNSC differentiation and ultimate regional neuronal identity as a first step toward a future spinal cord injury treatment. To achieve this, we encapsulated rat aNSCs in chitosan-based hydrogels functionalized with immobilized azide-tagged interferon-γ inside a chitosan conduit. Then, we implanted these constructs in the subcutaneous tissues in the backs of rats in the cervical, thoracic, and lumbar regions for 4, 6, and 8 weeks. After harvesting the scaffolds, we analyzed cell differentiation qualitatively using immunohistochemical analysis and quantitatively using RT-qPCR. Results revealed that the hydrogels supported aNSC survival and differentiation up to 4 weeks in the subcutaneous environment as marked by the expression of several neurogenesis markers. Most interesting, the aNSCs expressed region-specific Hox genes corresponding to their region of implantation. This study lays the groundwork for further translational work to recapitulate the potentially undiscovered patterning cues in the subcutaneous tissue and provide support for the conceptual premise that our bioengineering approach can form caudalized region-specific neuroepithelium.
可能需要一种整合干细胞并能够利用现有线索的组合方法来再生受损的神经组织,并最终恢复神经功能。本研究调查了接种到生物材料构建体中的成年神经干细胞(aNSCs)在皮下成熟对aNSC分化及最终区域神经元特性的影响,作为未来脊髓损伤治疗的第一步。为实现这一目标,我们将大鼠aNSCs封装在壳聚糖导管内固定有叠氮标记干扰素-γ的壳聚糖基水凝胶中。然后,我们将这些构建体植入大鼠颈部、胸部和腰部背部的皮下组织中4、6和8周。收获支架后,我们通过免疫组织化学分析进行定性细胞分化分析,并通过RT-qPCR进行定量分析。结果显示,水凝胶在皮下环境中支持aNSC存活和分化长达4周,这由几种神经发生标记物的表达所表明。最有趣的是,aNSCs表达与其植入区域相对应的区域特异性Hox基因。本研究为进一步的转化工作奠定了基础,以重现皮下组织中潜在未被发现的模式线索,并为我们的生物工程方法可形成尾侧化区域特异性神经上皮的概念前提提供支持。