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首页> 外文期刊>Acta biomaterialia >Relationship between scaffold channel diameter and number of regenerating axons in the transected rat spinal cord.
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Relationship between scaffold channel diameter and number of regenerating axons in the transected rat spinal cord.

机译:横断大鼠脊髓中支架通道直径与再生轴突数量之间的关系。

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Regeneration of endogenous axons through a Schwann cell (SC)-seeded scaffold implant has been demonstrated in the transected rat spinal cord. The formation of a cellular lining in the scaffold channel may limit the degree of axonal regeneration. Spinal cords of adult rats were transected and implanted with the SC-loaded polylactic co-glycollic acid (PLGA) scaffold implants containing seven parallel-aligned channels, either 450mum (n=19) or 660microm in diameter (n=14). Animals were sacrificed after 1, 2 and 3months. Immunohistochemistry for neurofilament expression was performed. The cross-sectional area of fibrous tissue and regenerative core was calculated. We found that the 450microm scaffolds had significantly greater axon fibers per channel at the 1month (186+/-37) and 3month (78+/-11) endpoints than the 660microm scaffolds (90+/-19 and 40+/-6, respectively) (p=0.0164 and 0.0149, respectively). The difference in the area of fibrous rim between the 450 and 660microm channels was most pronounced at the 1month endpoint, at 28,046+/-6551 and 58,633+/-7063microm(2), respectively (p=0.0105). Our study suggests that fabricating scaffolds with smaller diameter channels promotes greater regeneration over larger diameter channels. Axonal regeneration was reduced in the larger channels due to the generation of a large fibrous rim. Optimization of this scaffold environment establishes a platform for future studies of the effects of cell types, trophic factors or pharmacological agents on the regenerative capacity of the injured spinal cord.
机译:在横切的大鼠脊髓中已经证明了通过施万细胞(SC)植入的支架植入物可再生内源性轴突。支架通道中细胞衬里的形成可能会限制轴突再生的程度。将成年大鼠的脊髓横断并植入SC负载的聚乳酸共乙醇酸(PLGA)支架植入物,该植入物包含七个平行排列的通道,直径为450um(n = 19)或660microm(n = 14)。在1、2和3个月后处死动物。进行了神经丝表达的免疫组织化学。计算纤维组织和再生芯的横截面积。我们发现450微米支架在1个月(186 +/- 37)和3个月(78 +/- 11)终点具有比660微米支架(90 +/- 19和40 +/- 6)更高的每通道轴突纤维。分别为(p = 0.0164和0.0149)。 450和660微米通道之间的纤维边缘面积差异在1个月终点时最为明显,分别为28,046 +/- 6551和58,633 +/- 7063microm(2)(p = 0.0105)。我们的研究表明,制造直径较小的通道的支架可以促进直径较大的通道的再生。由于较大的纤维边缘的产生,在较大的通道中轴突再生减少。该支架环境的优化为将来研究细胞类型,营养因子或药理剂对受损脊髓的再生能力的影响建立了平台。

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