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高脂肪饮食诱导的代谢紊乱对角膜神经免疫特征的影响。

The effect of high-fat diet-induced metabolic disturbance on corneal neuroimmune features.

机构信息

Department of Optometry and Vision Sciences, The University of Melbourne, Parkville, Victoria, Australia.

Department of Anatomy and Neuroscience, The University of Melbourne, Parkville, Victoria, Australia.

出版信息

Exp Eye Res. 2020 Dec;201:108298. doi: 10.1016/j.exer.2020.108298. Epub 2020 Oct 15.

Abstract

PURPOSE

The highly innervated cornea is susceptible to nerve loss secondary to systemic diseases such as diabetes and metabolic disturbances caused by high-fat diet. In this study, we characterize the effect of high-fat diet on the mouse corneal neuroimmune phenotype, including changes to corneal nerve density and resident immune cells, alongside the clinical assessment of corneal thickness and endothelial cell density.

METHODS

Male C57Bl6/J mice, aged 10 weeks, were fed a high-fat diet (60 kcal% fat, 5.2 kcal/g) or control diet (10 kcal%, 3.8 kcal/g) for 16 weeks. At the study endpoint, metabolic parameters (HbA1c, weight, fasting glucose, body fat) were measured to confirm metabolic disturbance. Clinical imaging of the anterior segment was performed using optical coherence tomography to measure the corneal epithelial and stromal thickness. Corneal sensory nerves were visualized using flatmount immunostaining and confocal microscopy. The topographical distribution and density of sensory nerves (BIII-tubulin), intraepithelial CD45 and MHC- II cells, stromal macrophages (IBA1CD206) and endothelial cells (ZO-1) were analysed using FIJI.

RESULTS

High-fat diet mice had significantly higher blood HbA1c, higher body weight, a higher percentage of body fat and elevated fasting glucose compared to the control diet mice. Corneal epithelial and stromal thickness was similar in both groups. The sum length of the basal nerve plexus was lower in the central and peripheral cornea of mice fed a high-fat diet. In contrast, the sum length of superficial nerve terminals was similar between groups. Epithelial immune cell density was two-fold higher in the central corneas of high-fat diet mice compared to control diet mice. IBA1CD206 macrophage density was similar in the anterior stroma of both groups but was significantly higher in the posterior stroma of the peripheral cornea in the high-fat diet mice compared to controls. The percentage of nerve-associated MHC-II cells in the epithelium and stroma was higher in HFD mice compared to controls. Endothelial cell density was similar in the corneas of high-fat diet mice compared to controls.

CONCLUSION

Together with corneal neuropathy, corneal immune cells in mice fed a high-fat diet were differentially affected depending on their topographical distribution and location within cornea, and appeared in closer proximity to epithelial and stromal nerves, suggesting a local neuroimmune disruption induced by systemic metabolic disturbance.

摘要

目的

富含神经的角膜容易因糖尿病等系统性疾病或高脂肪饮食引起的代谢紊乱而导致神经丧失。在这项研究中,我们描述了高脂肪饮食对小鼠角膜神经免疫表型的影响,包括角膜神经密度和固有免疫细胞的变化,同时评估了角膜厚度和内皮细胞密度的临床变化。

方法

10 周龄雄性 C57Bl6/J 小鼠分别喂食高脂肪饮食(60%卡路里来自脂肪,5.2 卡路里/克)或对照饮食(10%卡路里来自脂肪,3.8 卡路里/克)16 周。在研究终点时,通过测量代谢参数(HbA1c、体重、空腹血糖、体脂)来确认代谢紊乱。使用光学相干断层扫描对眼前节进行临床成像,以测量角膜上皮和基质厚度。通过平皿免疫染色和共聚焦显微镜观察角膜感觉神经。使用 FIJI 分析感觉神经(BIII-微管蛋白)、上皮内 CD45 和 MHC-II 细胞、基质巨噬细胞(IBA1CD206)和内皮细胞(ZO-1)的拓扑分布和密度。

结果

与对照饮食组相比,高脂肪饮食组小鼠的血液 HbA1c 显著升高,体重、体脂百分比和空腹血糖升高。两组的角膜上皮和基质厚度相似。中央和周边角膜的基底神经丛总长度在高脂肪饮食组小鼠中较低。相比之下,两组的浅层神经末梢总长度相似。与对照饮食组相比,高脂肪饮食组小鼠中央角膜上皮免疫细胞密度增加了一倍。两组前基质中 IBA1CD206 巨噬细胞密度相似,但在周边角膜的后基质中,高脂肪饮食组小鼠的密度显著高于对照组。与对照组相比,角膜上皮和基质中与神经相关的 MHC-II 细胞的比例在 HFD 小鼠中更高。与对照组相比,高脂肪饮食组小鼠的角膜内皮细胞密度相似。

结论

与对照饮食组相比,喂食高脂肪饮食的小鼠角膜神经病变,其角膜免疫细胞也根据其在角膜中的拓扑分布和位置而受到不同的影响,且这些免疫细胞似乎更接近上皮和基质神经,提示系统性代谢紊乱引起的局部神经免疫紊乱。

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