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首页> 外文期刊>Neurochemical research >Pigment epithelium-derived factor released by mü ller glial cells exerts neuroprotective effects on retinal ganglion cells
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Pigment epithelium-derived factor released by mü ller glial cells exerts neuroprotective effects on retinal ganglion cells

机译:米勒神经胶质细胞释放的色素上皮衍生因子对视网膜神经节细胞发挥神经保护作用

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摘要

Survival of retinal ganglion cells (RGC) is compromised in several vision-threatening disorders such as ischemic and hypertensive retinopathies and glaucoma. Pigment epithelium-derived factor (PEDF) is a naturally occurring pleiotropic secreted factor in the retina. PEDF produced by retinal glial (Müller) cells is suspected to be an essential component of neuron-glial interactions especially for RGC, as it can protect this neuronal type from ischemia-induced cell death. Here we show that PEDF treatment can directly affect RGC survival in vitro. Using Müller cell-RGC-co-cultures we observed that activity of Müller-cell derived soluble mediators can attenuate hypoxia-induced damage and RGC loss. Finally, neutralizing the activity of PEDF in glia-conditioned media partially abolished the neuroprotective effect of glia, leading to an increased neuronal death in hypoxic condition. Altogether our results suggest that PEDF is crucially involved in the neuroprotective process of reactive Müller cells towards RGC.
机译:视网膜神经节细胞(RGC)的存活在几种威胁视力的疾病中受损,例如缺血性和高血压性视网膜病和青光眼。色素上皮衍生因子(PEDF)是视网膜中天然存在的多效性分泌因子。视网膜胶质细胞(Müller)产生的PEDF被怀疑是神经元-神经胶质相互作用的重要组成部分,尤其是对于RGC,因为它可以保护这种神经元类型免受局部缺血诱导的细胞死亡。在这里,我们显示PEDF治疗可以直接影响体外RGC的存活率。使用Müller细胞-RGC-共培养物,我们观察到Müller细胞衍生的可溶性介体的活性可以减弱缺氧诱导的损伤和RGC丧失。最后,在胶质细胞条件培养基中中和PEDF的活性部分消除了胶质细胞的神经保护作用,导致缺氧条件下神经元死亡的增加。总之,我们的结果表明PEDF参与了反应性Müller细胞对RGC的神经保护过程。

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