Santos Daniel, González-Pérez Francisco, Giudetti Guido, Micera Silvestro, Udina Esther, Del Valle Jaume, Navarro Xavier
Institute of Neurosciences and Department of Cell Biology, Physiology and Immunology, Universitat Autònoma de Barcelona, E-08193 Bellaterra, Spain.
Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED), E-08193 Bellaterra, Spain.
Int J Mol Sci. 2016 Dec 29;18(1):65. doi: 10.3390/ijms18010065.
After peripheral nerve injury, motor and sensory axons are able to regenerate but inaccuracy of target reinnervation leads to poor functional recovery. Extracellular matrix (ECM) components and neurotrophic factors (NTFs) exert their effect on different neuronal populations creating a suitable environment to promote axonal growth. Here, we assessed in vitro and in vivo the selective effects of combining different ECM components with NTFs on motor and sensory axons regeneration and target reinnervation. Organotypic cultures with collagen, laminin and nerve growth factor (NGF)/neurotrophin-3 (NT3) or collagen, fibronectin and brain-derived neurotrophic factor (BDNF) selectively enhanced sensory neurite outgrowth of DRG neurons and motor neurite outgrowth from spinal cord slices respectively. For in vivo studies, the rat sciatic nerve was transected and repaired with a silicone tube filled with a collagen and laminin matrix with NGF/NT3 encapsulated in poly(lactic-co-glycolic acid) (PLGA) microspheres (MP) (LM + MP.NGF/NT3), or a collagen and fibronectin matrix with BDNF in PLGA MPs (FN + MP.BDNF). Retrograde labeling and functional tests showed that LM + MP.NGF/NT3 increased the number of regenerated sensory neurons and improved sensory functional recovery, whereas FN + MP.BDNF preferentially increased regenerated motoneurons and enhanced motor functional recovery. Therefore, combination of ECM molecules with NTFs may be a good approach to selectively enhance motor and sensory axons regeneration and promote appropriate target reinnervation.
周围神经损伤后,运动和感觉轴突能够再生,但靶标再支配的不准确导致功能恢复不佳。细胞外基质(ECM)成分和神经营养因子(NTF)对不同的神经元群体发挥作用,营造一个促进轴突生长的合适环境。在此,我们在体外和体内评估了将不同的ECM成分与NTF结合对运动和感觉轴突再生以及靶标再支配的选择性影响。含有胶原蛋白、层粘连蛋白和神经生长因子(NGF)/神经营养因子-3(NT3)的器官型培养物,或含有胶原蛋白、纤连蛋白和脑源性神经营养因子(BDNF)的器官型培养物,分别选择性地增强了背根神经节(DRG)神经元的感觉神经突生长和脊髓切片中运动神经突的生长。对于体内研究,切断大鼠坐骨神经,并用填充有胶原蛋白和层粘连蛋白基质且NGF/NT3封装于聚乳酸-羟基乙酸共聚物(PLGA)微球(MP)中的硅胶管(LM + MP.NGF/NT3),或填充有胶原蛋白和纤连蛋白基质且BDNF存在于PLGA微球中的硅胶管(FN + MP.BDNF)进行修复。逆行标记和功能测试表明,LM + MP.NGF/NT3增加了再生感觉神经元的数量并改善了感觉功能恢复,而FN + MP.BDNF优先增加了再生运动神经元的数量并增强了运动功能恢复。因此,将ECM分子与NTF结合可能是选择性增强运动和感觉轴突再生并促进适当靶标再支配的一种良好方法。