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首页> 外文期刊>Experimental Eye Research >Bilateral early activation of retinal microglial cells in a mouse model of unilateral laser-induced experimental ocular hypertension
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Bilateral early activation of retinal microglial cells in a mouse model of unilateral laser-induced experimental ocular hypertension

机译:单侧激光诱导的实验眼高血压小鼠模型中视网膜微胶质细胞的双侧早期活化

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摘要

The immune system plays an important role in glaucomatous neurodegeneration. Retinal microglial reactivation associated with ganglion cell loss could reportedly contribute to the glaucoma progression. Recently we have described signs of microglia activation both in contralateral and ocular hypertension (OHT) eyes involving all retinal layers 15 days after OHT laser induction in mice. However, no works available have analyzed the microglial activation at earliest time points after OHT induction (24 h) in this experimental model. Thus, we seek to describe and quantify signs of microglia activation and differences depending on the retinal layer, 24 h after unilateral laser-induced OHT. Two groups of adult Swiss mice were used: age-matched control (naive) and lasered. In the lasered animals, OHT eyes as well as contralateral eyes were analyzed. Retinal whole-mounts were immunostained with antibodies against Iba-1 and MHC-II. We quantified the number of microglial cells in the photoreceptor layer (OS), outer plexiform layer (OPL), and inner plexiform layer (IPL); the number of microglial vertical processes connecting the OPL and OS; the area of the retina occupied by Iba-1 + cells (Ibal -RA) in the nerve fiber layer-ganglion cell layer (NFL-GCL), the total arbor area of microglial cells in the OPL and IPL and; Iba-1 + cell body area in the OPL, IPL and NFL-GCL. In contralateral and OHT eyes the morphological features of Iba-1 + cell activation were: migration, enlargement of the cell body, higher degree of branching and reorientation of the processes, radial disposition of the soma and processes toward adjacent microglial plexuses, and presence of amoeboid cells acting as macrophages. These signs were more pronounced in OHT eyes. Most of Iba-1 + cells did not express MHC-II; rather, only dendritic and rounded cells expressed it. In comparison with naive eyes, in OHT eyes and contralateral eyes no significant differences were found in the microglial cell number; but there was a significant increase in Iba1-RA. The total arbor area of microglial cells was significantly decreased in: i) OHT eyes with respect contralateral eyes and naive-eyes in IPL; ii) OHT eyes with respect to naive eyes in OPL. The number of microglial vertical processes connecting the OPL and OS were significantly increased in contralateral eyes compared with naive-eyes and OHT eyes. In OPL, IPL and NFL-GCL, the cell body area of Iba-1 + cells was significantly greater in OHT eyes than in naive and contralateral eyes, and greater in contralateral eyes than in naive eyes. A non-proliferative microglial reactivation was detected both in contralateral eyes and in OHT eyes in an early time after unilateral laser-induced OHT (24 h). This fast microglial activation, which involves the contralateral eye, could be mediated by the immune system.
机译:免疫系统在青光瘤神经变性中起重要作用。据报道,与神经节细胞损失有关的视网膜微胶质再活化会导致青光眼进展。最近,我们描述了在OHT激光诱导在小鼠中的所有视网膜层的对侧和眼高血压(OHT)眼中的微血花症活化迹象。然而,在该实验模型中,在OHT诱导(24小时)之后,不可用的作品已经在最早的时间点处于最早的时间点。因此,我们寻求描述和量化微血花植物激活和差异的迹象,这取决于视网膜层,在单侧激光引起的OHT之后24小时。使用两组成人瑞士小鼠:年龄匹配的控制(天真)并激发。在激发的动物中,分析了OHT眼睛以及对侧眼睛。用针对IBA-1和MHC-II的抗体免疫接种整体型材。我们量化了光感受器层(OS),外丛状层(OPL)和内部络植物层(IPL)中的小胶质细胞数量;连接OPL和OS的小胶质垂直过程的数量;在神经纤维层神经节细胞层(NFL-GCL)中的IBA-1 +细胞(Ibal -RA)占据的视网膜区域,OPL和IPL中的小胶质细胞的总Arbor面积。 OPL,IPL和NFL-GCL中的IBA-1 +细胞体积。在对侧和OHT眼睛中,IBA-1 +细胞活化的形态特征是:迁移,细胞体积,较高程度的分支和过程的重新定位,SOMA的径向布置和朝向相邻的小胶囊丛的过程,以及存在作用于巨噬细胞的作用细胞。这些迹象在oht眼睛中更加明显。大多数IBA-1 +细胞没有表达MHC-II;相反,只有树枝状和圆形细胞表达它。与幼稚的眼睛相比,在OHT的眼睛和对侧眼睛中,在微胶质细胞数中没有发现显着差异;但IBA1-RA有显着增加。微胶质细胞的总轴表面积显着降低:i)在IPL中尊重对侧眼睛和天真的眼睛的眼睛; ii)在OPL中对幼稚的眼睛的眼睛。与天真的眼睛和眼睛的眼睛相比,连接OPL和OS连接OPL和OS的微胶囊垂直过程的数量显着增加。在OPL,IPL和NFL-GCL中,IBA-1 +细胞的细胞体积在OHT眼睛中显着大于幼稚和对侧眼睛,对侧眼中比幼稚眼睛更大。在单侧激光诱导的OHT(24小时)后,在对侧眼睛和OHT眼中检测到不增殖的微胶质再活化。这种快速的微胶质激活,涉及对侧眼,可以由免疫系统介导。

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