Suppr超能文献

胰岛素样生长因子-I和胰岛素样生长因子结合蛋白-3在角膜伤口愈合过程中对角膜成纤维细胞的影响。

Involvement of insulin-like growth factor-I and insulin-like growth factor binding protein-3 in corneal fibroblasts during corneal wound healing.

作者信息

Izumi Kanako, Kurosaka Daijiro, Iwata Takeshi, Oguchi Yoshihisa, Tanaka Yasuhiko, Mashima Yukihiko, Tsubota Kazuo

机构信息

Department of Ophthalmology, Keio University School of Medicine, Tokyo, Japan.

出版信息

Invest Ophthalmol Vis Sci. 2006 Feb;47(2):591-8. doi: 10.1167/iovs.05-0097.

Abstract

PURPOSE

The involvement of downstream messengers of transforming growth factor (TGF)-beta in the differentiation of corneal fibroblasts into myofibroblasts was investigated. The effects of insulin-like growth factor (IGF)-I and insulin-like growth factor binding protein (IGFBP)-3 upregulated by TGF-beta were examined in human corneal fibroblasts, and the possible involvement of IGF axis components in corneal wound healing was assessed in a mouse model.

METHODS

Human corneal fibroblasts were incubated with TGF-beta2 or IGF-I, to investigate IGF-I, IGF-II, IGFBP-3, type I collagen, and alpha-smooth muscle actin (alpha-SMA) mRNA, as well as IGFBP-3 protein expression, during myofibroblast differentiation. DNA synthesis was evaluated with a 5-bromo-2'-deoxyuridine (BrdU) incorporation assay. IGFBP-3 mRNA expression, protein expression, and immunolocalization were investigated in mouse corneas after photorefractive keratectomy (PRK).

RESULTS

TGF-beta2 treatment induced expression of IGF-I and IGFBP-3 mRNA and of IGFBP-3 protein in human corneal fibroblasts. TGF-beta2 and IGF-I both stimulated expression of type I collagen. TGF-beta2 but not IGF-I potently stimulated alpha-SMA mRNA expression. IGF-I potently stimulated basal DNA synthesis, whereas IGFBP-3 inhibited it. IGF-I potently stimulated proliferation of TGF-beta2-activated myofibroblasts without reversing the activated fibrogenic phenotype, whereas IGFBP-3 suppressed IGF-I-induced proliferation of corneal fibroblasts. IGFBP-3 mRNA and protein increased in mouse corneas soon after PRK, when in vivo immunostaining of the corneas showed expression of IGFBP-3 in the deep layer of the corneal stroma.

CONCLUSIONS

These results suggest that during corneal wound healing, TGF-beta stimulates IGF axis components, whereas IGFBP-3 may modulate IGF-I-induced myofibroblast proliferation to suppress corneal mesenchymal overgrowth.

摘要

目的

研究转化生长因子(TGF)-β下游信号分子在角膜成纤维细胞向肌成纤维细胞分化中的作用。检测TGF-β上调的胰岛素样生长因子(IGF)-I和胰岛素样生长因子结合蛋白(IGFBP)-3对人角膜成纤维细胞的影响,并在小鼠模型中评估IGF轴成分在角膜伤口愈合中的可能作用。

方法

将人角膜成纤维细胞与TGF-β2或IGF-I孵育,以研究在肌成纤维细胞分化过程中IGF-I、IGF-II、IGFBP-3、I型胶原和α-平滑肌肌动蛋白(α-SMA)mRNA以及IGFBP-3蛋白的表达。用5-溴-2'-脱氧尿苷(BrdU)掺入法评估DNA合成。在准分子激光角膜切削术(PRK)后,研究小鼠角膜中IGFBP-3 mRNA表达、蛋白表达和免疫定位。

结果

TGF-β2处理可诱导人角膜成纤维细胞中IGF-I和IGFBP-3 mRNA以及IGFBP-3蛋白的表达。TGF-β2和IGF-I均刺激I型胶原的表达。TGF-β2能有效刺激α-SMA mRNA表达,而IGF-I不能。IGF-I能有效刺激基础DNA合成,而IGFBP-3则抑制它。IGF-I能有效刺激TGF-β2激活的肌成纤维细胞增殖,而不逆转激活的纤维化表型,而IGFBP-3则抑制IGF-I诱导的角膜成纤维细胞增殖。PRK后小鼠角膜中IGFBP-3 mRNA和蛋白很快增加,此时角膜的体内免疫染色显示IGFBP-3在角膜基质深层表达。

结论

这些结果表明,在角膜伤口愈合过程中,TGF-β刺激IGF轴成分,而IGFBP-3可能调节IGF-I诱导的肌成纤维细胞增殖,以抑制角膜间质过度生长。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验