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血管内皮生长因子对外耳道胆脂瘤成纤维细胞的影响。

Effect of vascular endothelial growth factor on fibroblasts from external auditory canal cholesteatoma.

作者信息

Naim Ramin, Chang Ray C, Sadick Haneen, Bayerl Christiane, Bran Gregor, Hormann Karl

机构信息

Department of Otolaryngology, Head and Neck Surgery, University Hospital Mannheim, Germany.

出版信息

Arch Med Res. 2005 Sep-Oct;36(5):518-23. doi: 10.1016/j.arcmed.2005.03.042.

Abstract

BACKGROUND

EACC is a disease of the external auditory canal resulting in destruction of adjacent tissue. However, the role of the surrounding mesenchymal fibroblasts of the perimatrix still remains unclear. In this study we treat isolated fibroblasts of EACC with VEGF and determine FGF-2 levels. We also treat the fibroblast cultures with FGF-2 and measured VEGF levels.

METHODS

All EACC cell cultures were obtained from five patients undergoing surgery and used at passage 3. After 1-4 days incubation with 50 ng/mL FGF-2, and 1-8 days incubation with 50 pg/mL VEGF incubation, the expression of the FGF-2 and VEGF protein in the supernatants of the HGF/SF-treated and -untreated culture cell lines was analyzed, respectively.

RESULTS

After 8 days of incubation with 50 ng/mL VEGF, the levels of FGF-2 decreased. However, after 4 days of incubation with FGF-2 the VEGF levels increased significantly in treated tissue culture (p <0.05) in comparison to untreated EACC fibroblasts. The total protein concentration showed no significant difference in both cultures (p >0.05).

CONCLUSIONS

In summary, exogenous FGF-2 increased fibroblast expression of VEGF, which is a major autocrine mediator of FGF-2-induced angiogenesis and proliferation. However, incubation with VEGF resulted in decrease of FGF-2 levels. Regarding the slow growth of the fibroblasts, they may not be as likely to exhibit a reactive or invasive phenotype as seen in middle ear cholesteatoma fibroblasts.

摘要

背景

外耳道腺样囊性癌(EACC)是一种外耳道疾病,可导致邻近组织破坏。然而,周围基质间充质成纤维细胞的作用仍不清楚。在本研究中,我们用血管内皮生长因子(VEGF)处理EACC分离的成纤维细胞并测定碱性成纤维细胞生长因子-2(FGF-2)水平。我们还用FGF-2处理成纤维细胞培养物并测量VEGF水平。

方法

所有EACC细胞培养物均取自5例接受手术的患者,并在第3代使用。在分别用50 ng/mL FGF-2孵育1 - 4天和用50 pg/mL VEGF孵育1 - 8天后,分别分析经肝细胞生长因子/散射因子(HGF/SF)处理和未处理的培养细胞系上清液中FGF-2和VEGF蛋白的表达。

结果

用50 ng/mL VEGF孵育8天后,FGF-2水平降低。然而,与未处理的EACC成纤维细胞相比,用FGF-2孵育4天后,处理后的组织培养物中VEGF水平显著升高(p <0.05)。两种培养物中的总蛋白浓度无显著差异(p >0.05)。

结论

总之,外源性FGF-2增加了成纤维细胞VEGF的表达,VEGF是FGF-2诱导血管生成和增殖的主要自分泌介质。然而,用VEGF孵育导致FGF-2水平降低。鉴于成纤维细胞生长缓慢,它们可能不太可能表现出中耳胆脂瘤成纤维细胞中所见的反应性或侵袭性表型。

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