FIBROBLAST GROWTH-FACTOR EFFECTS ON PERIPHERAL-NERVE REGENERATION IN A SILICONE CHAMBER MODEL

FIBROBLAST GROWTH-FACTOR EFFECTS ON PERIPHERAL-NERVE REGENERATION IN A SILICONE CHAMBER MODEL
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DOI:
10.1002/jnr.490200306
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发表时间:
1988-07-01
影响因子:
4.2
通讯作者:
VARON, S
VARON, S
中科院分区:
医学3区
文献类型:
--
作者:
DANIELSEN, N;PETTMANN, B;VARON, S

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我们开发了一种硅胶神经再生室,它被一条硝化纤维纸分成两个隔室。 The modified two-compartment chamber allows the investigation of the effects on rat sciatic nerve regeneration of trophic or growth factors that are initially bound to the nitrocellulose partition. In this study we compared the effects of untreated nitrocellulose, a siliconized nitrocellulose strip, and a strip that had been soaked in a basic fibroblast growth factor (FGF) solution. FGF 是一种已知的血管生成因子,也是内皮细胞、成纤维细胞和雪旺细胞的有丝分裂原。所有这些细胞类型都存在于周围神经中。 In vitro analyses, using 3T3 cells as test cells, showed that some of the bound FGF remained active on the nitrocellulose paper for at least 8-10 days. In vivo experiments, examined at 16 days post-implantation, revealed that spatial migration of all cellular elements (perineurial-like cells, vasculature, and Schwann cells) across the chamber gap was slower with untreated nitrocellulose strips than with siliconized strips but was most advanced with FGF-treated ones.最引人注目的是 FGF 室内再生体的发育良好的血管树枝化。 Histologic sections from the proximal one-half of the chamber revealed that the regenerate in untreated strip chambers consisted of fibrin matrix and erythrocytes, whereas a well-developed structure with all the cellular elements of a regenerating nerve was seen in several of the FGF strip chambers.我们得出结论,FGF 在此模型中刺激周围神经再生。
We have developed a silicone nerve regeneration chamber that is partitioned into two compartments by a strip of nitrocellulose paper. The modified two-compartment chamber allows the investigation of the effects on rat sciatic nerve regeneration of trophic or growth factors that are initially bound to the nitrocellulose partition. In this study we compared the effects of untreated nitrocellulose, a siliconized nitrocellulose strip, and a strip that had been soaked in a basic fibroblast growth factor (FGF) solution. FGF is a known angiogenic factor and a mitogen for endothelial cells, fibroblasts, and Schwann cells. All of these cell types are present in the peripheral nerve. In vitro analyses, using 3T3 cells as test cells, showed that some of the bound FGF remained active on the nitrocellulose paper for at least 8-10 days. In vivo experiments, examined at 16 days post-implantation, revealed that spatial migration of all cellular elements (perineurial-like cells, vasculature, and Schwann cells) across the chamber gap was slower with untreated nitrocellulose strips than with siliconized strips but was most advanced with FGF-treated ones. Most striking was the well-developed vascular arborization of the regenerate within the FGF chambers. Histologic sections from the proximal one-half of the chamber revealed that the regenerate in untreated strip chambers consisted of fibrin matrix and erythrocytes, whereas a well-developed structure with all the cellular elements of a regenerating nerve was seen in several of the FGF strip chambers. We conclude that FGF stimulates peripheral nerve regeneration in this model.