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Three-Dimensional Model of Dorsal Root Ganglion Explant as a Method of Studying Neurotrophic Factors in Regenerative Medicine

机译:背根神经节外植体三维模型作为研究再生医学中神经营养因子的方法

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摘要

Neurotrophic factors play a key role in the development, differentiation, and survival of neurons and nerve regeneration. In the present study, we evaluated the effect of certain neurotrophic factors (NGF, BDNF, and GDNF) on axon growth and migration of Nestin-green fluorescent protein (GFP)-positive cells using a 3D model of dorsal root ganglion (DRG) explant culture in Matrigel. Our method generally represents a convenient model for assessing the effects of soluble factors and therapeutic agents on axon growth and nerve regeneration in R&D studies. By analyzing the DRG explants in ex vivo culture for 21 days, one can evaluate the parameters of neurite outgrowth and the rate of cell migration from the DRG explants into the Matrigel. For the current study, we used Nestin-GFP-expressing mice in which neural precursors express Nestin and the green fluorescent protein (GFP) under the same promoter. We revealed that GDNF significantly (two fold) stimulated axon outgrowth ( < 0.05), but not BDNF or NGF. It is well-known that axon growth can be stimulated by activated glial cells that fulfill a trophic function for regenerating nerves. For this reason, we evaluated the number of Nestin-GFP-positive cells that migrated from the DRG into the Matrigel in our 3D ex vivo explant model. We found that NGF and GDNF, but not BDNF, stimulated the migration of Nestin-GFP cells compared to the control ( < 0.05). On the basis of the aforementioned finding, we concluded that GDNF had the greatest stimulating potential for axon regeneration, as it stimulated not only the axon outgrowth, but also glial cell migration. Although NGF significantly stimulated glial cell migration, its effect on axon growth was insufficient for axon regeneration.
机译:神经营养因子在神经元和神经再生的发育,分化和存活中起关键作用。在本研究中,我们使用背根神经节(DRG)外植体的3D模型评估了某些神经营养因子(NGF,BDNF和GDNF)对巢蛋白-绿色荧光蛋白(GFP)阳性细胞轴突生长和迁移的影响Matrigel的文化。我们的方法通常代表一个方便的模型,用于评估R&D研究中的可溶性因子和治疗剂对轴突生长和神经再生的影响。通过分析离体培养21天的DRG外植体,可以评估神经突向外生长的参数以及细胞从DRG外植体向基质胶的迁移速率。对于当前的研究,我们使用了表达Nestin-GFP的小鼠,其中神经前体在同一启动子下表达Nestin和绿色荧光蛋白(GFP)。我们发现GDNF显着(两倍)刺激轴突生长(<0.05),但不刺激BDNF或NGF。众所周知,激活神经胶质细胞可以刺激轴突的生长,这些神经胶质细胞具有使神经再生的营养功能。因此,我们评估了在我们的3D离体外植体模型中从DRG迁移到Matrigel中的Nestin-GFP阳性细胞的数量。我们发现与对照相比,NGF和GDNF而非BDNF刺激了Nestin-GFP细胞的迁移(<0.05)。根据上述发现,我们得出结论,GDNF具有最大的刺激轴突再生潜能,因为它不仅刺激轴突生长,而且刺激神经胶质细胞迁移。尽管NGF显着刺激神经胶质细胞迁移,但其对轴突生长的影响不足以促进轴突再生。

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