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年龄相关性黄斑变性患者中的CX3CL1/CX3CR1和CCL2/CCR2趋化因子/趋化因子受体复合物

CX3CL1/CX3CR1 and CCL2/CCR2 chemokine/chemokine receptor complex in patients with AMD.

作者信息

Falk Mads Krüger, Singh Amardeep, Faber Carsten, Nissen Mogens Holst, Hviid Thomas, Sørensen Torben Lykke

机构信息

Clinical Eye Research Unit, Department of Ophthalmology, Copenhagen University Hospital Roskilde, Roskilde, Denmark and Faculty of Health Sciences, University of Copenhagen, Copenhagen, Denmark.

Department of Microbiology, Immunology & International Health, Faculty of Health Sciences, University of Copenhagen, Copenhagen, Denmark; Department of Ophthalmology, Glostrup Hospital, Glostrup, Denmark.

出版信息

PLoS One. 2014 Dec 15;9(12):e112473. doi: 10.1371/journal.pone.0112473. eCollection 2014.

Abstract

PURPOSE

The chemokine receptors CX3CR1 and CCR2 have been implicated in the development of age-related macular degeneration (AMD). The evidence is mainly derived from experimental cell studies and murine models of AMD. The purpose of this study was to investigate the association between expression of CX3CR1 and CCR2 on different leukocyte subsets and AMD. Furthermore we measured the plasma levels of ligands CX3CL1 and CCL2.

METHODS

Patients attending our department were asked to participate in the study. The diagnosis of AMD was based on clinical examination and multimodal imaging techniques. Chemokine plasma level and chemokine receptor expression were measured by flow-cytometry.

RESULTS

A total of 150 participants were included. We found a significantly lower expression of CX3CR1 on CD8+ T cells in the neovascular AMD group compared to the control group (p = 0.04). We found a significant positive correlation between CCR2 and CX3CR1 expression on CD8+ cells (r = 0.727, p = 0.0001). We found no difference in plasma levels of CX3CL1 and CCL2 among the groups.

CONCLUSIONS

Our results show a down regulation of CX3CR1 on CD8+ cells; this correlated to a low expression of CCR2 on CD8+ cells. Further studies are needed to elucidate the possible role of this cell type in AMD development.

摘要

目的

趋化因子受体CX3CR1和CCR2与年龄相关性黄斑变性(AMD)的发生发展有关。证据主要来自实验性细胞研究和AMD小鼠模型。本研究的目的是调查不同白细胞亚群上CX3CR1和CCR2的表达与AMD之间的关联。此外,我们还测量了配体CX3CL1和CCL2的血浆水平。

方法

邀请我院就诊的患者参与本研究。AMD的诊断基于临床检查和多模态成像技术。通过流式细胞术测量趋化因子血浆水平和趋化因子受体表达。

结果

共纳入150名参与者。我们发现,与对照组相比,新生血管性AMD组CD8+T细胞上CX3CR1的表达显著降低(p = 0.04)。我们发现CD8+细胞上CCR2与CX3CR1的表达之间存在显著正相关(r = 0.727,p = 0.0001)。我们发现各组间CX3CL1和CCL2的血浆水平无差异。

结论

我们的结果显示CD8+细胞上CX3CR1表达下调;这与CD8+细胞上CCR2的低表达相关。需要进一步研究以阐明这种细胞类型在AMD发生发展中的可能作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/491a/4266494/6542d5b1afbb/pone.0112473.g001.jpg

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