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[外耳道胆脂瘤-成纤维细胞培养中的血管生成因子]

[Angiogenic factors in external auditory canal cholesteatoma-fibroblast cell culture].

作者信息

Naim R, Sadick H, Bayerl C, Bran G, Hörmann K

机构信息

Universitäts-Hals-Nasen-Ohren-Klinik, Mannheim.

出版信息

HNO. 2005 Nov;53(11):952-6. doi: 10.1007/s00106-005-1252-z.

Abstract

BACKGROUND

The external auditory canal cholesteatoma (EACC) is characterized by hyperproliferation of the epithelial and subepithelial tissue. Compared to normal meatal skin, strong expression of FGF-2 and VEGF had previously been detected. Many authors reported that FGF-2 acts via VEGF and is induced by hypoxia. Hypoxia seems to be pivotal for establishing EACC. Therefore, human EACC fibroblasts were investigated by incubating with FGF-2 and determining VEGF.

PATIENTS AND METHODS

We harvested fibroblasts from human EACC and normal meatal skin and incubated the fibroblast culture with 50 ng/ml FGF-2 and determined VEGF concentrations after 1-4 days.

RESULTS

Compared to untreated fibroblast cultures, there was a significant increase of VEGF concentration (p<0.05). However, there was no significant difference between the proliferation quantities.

CONCLUSION

VEGF and FGF-2 are possibly involved in a cascade of growth factor activities, which modulates their concentration in human-derived EACC fibroblast culture. Exogenous FGF-2 increased fibroblast expression for VEGF, which is a major autocrine mediator of FGF-2-induced angiogenesis and proliferation.

摘要

背景

外耳道胆脂瘤(EACC)的特征是上皮和上皮下组织过度增殖。与正常耳道皮肤相比,先前已检测到FGF-2和VEGF的强表达。许多作者报道FGF-2通过VEGF起作用并由缺氧诱导。缺氧似乎是EACC形成的关键因素。因此,通过用FGF-2孵育人EACC成纤维细胞并测定VEGF来进行研究。

患者和方法

我们从人EACC和正常耳道皮肤中获取成纤维细胞,并用50 ng/ml FGF-2孵育成纤维细胞培养物,并在1-4天后测定VEGF浓度。

结果

与未处理的成纤维细胞培养物相比,VEGF浓度有显著增加(p<0.05)。然而,增殖量之间没有显著差异。

结论

VEGF和FGF-2可能参与了一系列生长因子活动,这些活动调节了它们在人源EACC成纤维细胞培养物中的浓度。外源性FGF-2增加了成纤维细胞对VEGF的表达,VEGF是FGF-2诱导的血管生成和增殖的主要自分泌介质。

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