Kamiya Kazutaka, Wang Mingcong, Uchida Saiko, Amano Shiro, Oshika Tetsuro, Sakuragawa Norio, Hori Junko
Department of Ophthalmology, University of Tokyo School of Medicine, Tokyo, Japan.
Exp Eye Res. 2005 May;80(5):671-9. doi: 10.1016/j.exer.2004.11.018. Epub 2005 Jan 19.
Human amniotic epithelial cells (HAEC) may be a source of soluble anti-inflammatory factors. The purpose of this study is to determine the effect of topically applied HAEC culture supernatant on corneal inflammatory reactions. HAEC were obtained from a placenta and cultured for 48 hr, and the supernatant was collected. The conditioned medium from HAEC contained small amounts of human interleukin-1 receptor antagonist (IL-1ra). Intrastromal sutures were placed in the cornea of BALB/c mice to induce corneal neovascularisation. Superficial cauterisation was applied to induce recruitment or activation of antigen presenting cells (APCs) in the cornea without neovascularisation. HAEC conditioned medium, placebo, or recombinant human IL-1ra was topically applied three times daily for 2 weeks. Suture-induced corneal neovascularisation was evaluated microscopically for 8 weeks. The cauterised corneas were harvested at 2 weeks, and the MHC class II(+) APCs were quantified by immunofluorescent staining and confocal microscopy. Inflammatory cytokine gene expression in the cauterised corneas was analyzed by a multiprobe ribonuclease protection assay. Conditioned medium from HAEC led to a profound suppression of corneal neovascularisation and fewer MHC class II(+) APCs in the epithelium. In contrast, human IL-1ra was only slightly effective in suppressing corneal inflammatory reactions. mRNA expression of murine IL-1ra and IL-1beta in the cauterised corneas was markedly suppressed after application of the conditioned medium. These results suggest that HAEC are a source of soluble anti-inflammatory factors and that conditioned medium from HAEC contains factors other than IL-1ra that suppress corneal inflammation.
人羊膜上皮细胞(HAEC)可能是可溶性抗炎因子的一个来源。本研究的目的是确定局部应用HAEC培养上清液对角膜炎症反应的影响。从胎盘获取HAEC并培养48小时,然后收集上清液。HAEC的条件培养基中含有少量的人白细胞介素-1受体拮抗剂(IL-1ra)。在BALB/c小鼠的角膜内植入基质缝线以诱导角膜新生血管形成。对无新生血管的角膜进行表面烧灼以诱导抗原呈递细胞(APC)的募集或激活。每天局部应用HAEC条件培养基、安慰剂或重组人IL-1ra三次,持续2周。在8周内通过显微镜评估缝线诱导的角膜新生血管形成情况。在2周时收获烧灼的角膜,通过免疫荧光染色和共聚焦显微镜对MHC II类(+)APC进行定量。通过多探针核糖核酸酶保护试验分析烧灼角膜中炎性细胞因子基因的表达。HAEC的条件培养基可显著抑制角膜新生血管形成,并使上皮中的MHC II类(+)APC减少。相比之下,人IL-1ra在抑制角膜炎症反应方面仅略有效果。应用条件培养基后,烧灼角膜中鼠IL-1ra和IL-1β的mRNA表达明显受到抑制。这些结果表明,HAEC是可溶性抗炎因子的一个来源,并且HAEC的条件培养基中含有除IL-1ra之外的其他抑制角膜炎症的因子。