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实验性自身免疫性青光眼模型中视网膜和视神经通过凝集素途径的补体同时反应

Simultaneous Complement Response via Lectin Pathway in Retina and Optic Nerve in an Experimental Autoimmune Glaucoma Model.

作者信息

Reinehr Sabrina, Reinhard Jacqueline, Gandej Marcel, Kuehn Sandra, Noristani Rozina, Faissner Andreas, Dick H Burkhard, Joachim Stephanie C

机构信息

Experimental Eye Research Institute, University Eye Hospital, Ruhr-University Bochum Bochum, Germany.

Department of Cell Morphology and Molecular Neurobiology, Faculty of Biology and Biotechnology, Ruhr-University Bochum Bochum, Germany.

出版信息

Front Cell Neurosci. 2016 Jun 1;10:140. doi: 10.3389/fncel.2016.00140. eCollection 2016.

Abstract

Glaucoma is a multifactorial disease and especially mechanisms occurring independently from an elevated intraocular pressure (IOP) are still unknown. Likely, the immune system contributes to the glaucoma pathogenesis. Previously, IgG antibody depositions and retinal ganglion cell (RGC) loss were found in an IOP-independent autoimmune glaucoma model. Therefore, we investigated the possible participation of the complement system in this model. Here, rats were immunized with bovine optic nerve homogenate antigen (ONA), while controls (Co) received sodium chloride (n = 5-6/group). After 14 days, RGC density was quantified on flatmounts. No changes in the number of RGCs could be observed at this point in time. Longitudinal optic nerve sections were stained against the myelin basic protein (MBP). We could note few signs of degeneration processes. In order to detect distinct complement components, retinas and optic nerves were labeled with complement markers at 3, 7, 14, and 28 days and analyzed. Significantly more C3 and MAC depositions were found in retinas and optic nerves of the ONA group. These were already present at day 7, before RGC loss and demyelination occurred. Additionally, an upregulation of C3 protein was noted via Western Blot at this time. After 14 days, quantitative real-time PCR revealed significantly more C3 mRNA in the ONA retinas. An upregulation of the lectin pathway-associated mannose-serine-protease-2 (MASP2) was observed in the retinas as well as in the optic nerves of the ONA group after 7 days. Significantly more MASP2 in retinas could also be observed via Western Blot analyses at this point in time. No effect was noted in regard to C1q. Therefore, we assume that the immunization led to an activation of the complement system via the lectin pathway in retinas and optic nerves at an early stage in this glaucoma model. This activation seems to be an early response, which then triggers degeneration. These findings can help to develop novel therapy strategies for glaucoma patients.

摘要

青光眼是一种多因素疾病,尤其是那些独立于眼内压(IOP)升高而发生的机制仍不明确。免疫系统可能参与了青光眼的发病机制。此前,在一个不依赖眼内压的自身免疫性青光眼模型中发现了IgG抗体沉积和视网膜神经节细胞(RGC)丢失。因此,我们研究了补体系统在该模型中的可能参与情况。在此,用牛视神经匀浆抗原(ONA)免疫大鼠,而对照组(Co)注射氯化钠(每组n = 5 - 6只)。14天后,在视网膜铺片上对RGC密度进行定量分析。此时未观察到RGC数量的变化。对纵向视神经切片进行髓鞘碱性蛋白(MBP)染色。我们几乎没有发现退变过程的迹象。为了检测不同的补体成分,在第3、7、14和28天用补体标记物对视网膜和视神经进行标记并分析。在ONA组的视网膜和视神经中发现C3和膜攻击复合物(MAC)的沉积明显更多。这些在第7天就已出现,早于RGC丢失和脱髓鞘发生之前。此外,此时通过蛋白质印迹法注意到C3蛋白上调。14天后,定量实时PCR显示ONA组视网膜中C3 mRNA明显更多。7天后,在ONA组的视网膜和视神经中观察到凝集素途径相关的甘露糖 - 丝氨酸蛋白酶 - 2(MASP2)上调。此时通过蛋白质印迹分析在视网膜中也可观察到明显更多的MASP2。未观察到C1q有影响。因此,我们推测在这个青光眼模型的早期,免疫接种通过凝集素途径导致视网膜和视神经中的补体系统激活。这种激活似乎是一种早期反应,随后引发退变。这些发现有助于为青光眼患者开发新的治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51ec/4887475/97ad06479204/fncel-10-00140-g001.jpg

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