Izumi Kanako, Kurosaka Daijiro, Iwata Takeshi, Oguchi Yoshihisa, Tanaka Yasuhiko, Mashima Yukihiko, Tsubota Kazuo
Department of Ophthalmology, Keio University School of Medicine, Tokyo, Japan.
Invest Ophthalmol Vis Sci. 2006 Feb;47(2):591-8. doi: 10.1167/iovs.05-0097.
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.
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).
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.
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.
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。
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。
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。
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。