自然免疫与眼部炎症。

Koh-Hei Sonoda
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引用次数: 0

摘要

我们关注先天免疫在oföchoroidal新生血管(CNV)相关diseasesù形成过程中的作用。炎症影响各种玻璃体视网膜疾病的形成和发展。我们对糖尿病性黄斑水肿、增殖性糖尿病视网膜病变、视网膜分支静脉阻塞、视网膜中央静脉阻塞和孔源性视网膜脱离的玻璃体液中的炎症免疫介质进行了全面分析。同时测定20种可溶性因子(9种细胞因子、6种趋化因子和5种生长因子)的浓度。在20个可溶性因子中,有3个因子:白细胞介素-6 (IL-6)、白细胞介素-8 (IL-8)和单核细胞化学引诱蛋白-1 (MCP-1)在所有玻璃体视网膜疾病组中与对照组相比显著升高。根据个体患者水平的相关性分析,这三个因素同时升高,在所有被检查的疾病中均未显示出任何独立的上调。我们还阐明了自然杀伤(NK)T细胞在激光诱导的实验性CNV中的作用,NK T细胞限制CD1分子并参与先天免疫反应。我们在两个独立的NKT细胞缺陷小鼠(CD1敲除(KO)小鼠或Ja18 KOmice)中检测了CNV的形成,发现两种KO小鼠的实验CNV都显著减少。在CNV相关疾病的临床过程中,除了CNV的形成外,视网膜下的瘢痕形成被认为是另一个重要的步骤。因此,我们通过向视网膜下间隙注射腹腔渗出性巨噬细胞建立视网膜下瘢痕的实验模型。接种后7天,用眼底镜观察小鼠视网膜下纤维组织。组织呈单调低细胞密度区,表达a-SMA,胶原合成。由于epec接种的MCP-1 KO小鼠胶质细胞残留量较少,因此除了外源性巨噬细胞外,内源性巨噬细胞也至关重要。活化的巨噬细胞在体外直接诱导RPE细胞的肌纤维化改变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Natural Immunity and Ocular Inflammation.

We have focused on the role of innate immunity during the formation oföchoroidal neovascularization (CNV) -related diseasesù. Inflammation affects the formation and the progression of various vitreoretinal diseases. We performed a comprehensive analysis of inflammatory immune mediators in the vitreous fluids with diabetic macular edema, proliferative diabetic retinopathy, branch retinal vein occlusion, central retinal vein occlusion and rhegmatogenous retinal detachment. The concentrations of 20 soluble factors (nine cytokines, six chemokines, and five growth factors) were measured simultaneously by multiplex bead analysis system. Out of 20 soluble factors, three factors : interleukin-6 (IL-6), interleukin-8 (IL-8), and monocyte chemoattractant protein-1 (MCP-1) were significantly elevated in all groups of vitreoretinal diseases compared with control group. According to the correlation analysis in the individual patientʼs level, these three factors that were simultaneously increased, did not show any independent upregulation in all the examined diseases. We also elucidated the role of natural killer (NK)T cells, which restricted CD1 molecule and participate in the innate immune response, in laser-induced experimental CNV. We examined CNV formation in independent two NKT cell-deficient mice, either CD1 knockout (KO) mice or Ja18 KO mice, and found that both KO mice showed significant reduction of experimental CNV. During the clinical process of CNV-related diseases, not only CNV formation, subretinal scaring is thought to be another important step. We thus established the experimental model of subretinal scaring by injecting peritoneal exudating macrophages into subretinal space. Subretinal fibrous tissue was observed by fundus scope in PEC-inoculated mice after seven days. The tissue was consisted of monotonous and low cell-density area, which expressed a-SMA with collagen synthesis. Because PEC-inoculated MCP-1 KO mice showed less amount of glial residual, not only exogenous macrophages, but also intrinsic macrophages are critical. Activated macrophages directly induced myofibrotic changes in RPE cells in vitro.

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