通过分析间充质干细胞的分泌组鉴定血小板衍生生长因子赋予视网膜神经节细胞的神经保护作用。
Identification of retinal ganglion cell neuroprotection conferred by platelet-derived growth factor through analysis of the mesenchymal stem cell secretome.
机构信息
1 Section of Retinal Ganglion Cell Biology, Laboratory of Retinal Cell and Molecular Biology, National Eye Institute, National Institutes of Health, Bethesda, Maryland, 20892, USA.
出版信息
Brain. 2014 Feb;137(Pt 2):503-19. doi: 10.1093/brain/awt292. Epub 2013 Oct 30.
The development of neuroprotective strategies to attenuate retinal ganglion cell death could lead to novel therapies for chronic optic neuropathies such as glaucoma. Intravitreal transplantation of mesenchymal stem cells slows retinal ganglion cell death in models of optic nerve injury, but the mechanism of action remains unclear. Here we characterized the neuroprotective effects of mesenchymal stem cells and mesenchymal stem cell-derived factors in organotypic retinal explant culture and an in vivo model of ocular hypertensive glaucoma. Co-culture of rat and human bone marrow-derived mesenchymal stem cells with retinal explants increased retinal ganglion cell survival, after 7 days ex vivo, by ∼2-fold and was associated with reduced apoptosis and increased nerve fibre layer and inner plexiform layer thicknesses. These effects were not demonstrated by co-culture with human or mouse fibroblasts. Conditioned media from mesenchymal stem cells conferred neuroprotection, suggesting that the neuroprotection is mediated, at least partly, by secreted factors. We compared the concentrations of 29 factors in human mesenchymal stem cell and fibroblast conditioned media, and identified 11 enriched in the mesenchymal stem cell secretome. Treatment of retinal explants with a cocktail of these factors conferred retinal ganglion cell neuroprotection, with factors from the platelet-derived growth factor family being the most potent. Blockade of platelet-derived growth factor signalling with neutralizing antibody or with small molecule inhibitors of platelet-derived growth factor receptor kinase or downstream phosphatidylinositol 3 kinase eliminated retinal ganglion cell neuroprotection conferred by mesenchymal stem cell co-culture. Intravitreal injection of platelet-derived growth factor -AA or -AB led to profound optic nerve neuroprotection in vivo following experimental induction of elevated intraocular pressure. These data demonstrate that mesenchymal stem cells secrete a number of neuroprotective proteins and suggest that platelet-derived growth factor secretion in particular may play an important role in mesenchymal stem cell-mediated retinal ganglion cell neuroprotection. Furthermore, platelet-derived growth factor may represent an independent target for achieving retinal ganglion cell neuroprotection.
神经保护策略的发展可以减轻视网膜神经节细胞的死亡,从而为青光眼等慢性视神经病变提供新的治疗方法。间质干细胞的玻璃体内移植可减缓视神经损伤模型中的视网膜神经节细胞死亡,但作用机制尚不清楚。在这里,我们在器官型视网膜培养物和高眼压性青光眼的体内模型中,描述了间质干细胞及其衍生因子的神经保护作用。大鼠和人骨髓间充质干细胞与视网膜外植体共培养可使视网膜神经节细胞在体外培养 7 天后的存活率增加约 2 倍,并且与凋亡减少以及神经纤维层和内丛状层厚度增加有关。与人或鼠成纤维细胞共培养则不会产生这种效果。间质干细胞条件培养基赋予神经保护作用,提示这种神经保护作用至少部分是由分泌因子介导的。我们比较了人间质干细胞和成纤维细胞条件培养基中 29 种因子的浓度,并确定了 11 种在间质干细胞分泌组中富集的因子。用这些因子的鸡尾酒处理视网膜外植体可赋予视网膜神经节细胞神经保护作用,血小板衍生生长因子家族的因子最有效。用中和抗体或血小板衍生生长因子受体激酶或下游磷脂酰肌醇 3 激酶的小分子抑制剂阻断血小板衍生生长因子信号通路可消除间质干细胞共培养赋予的视网膜神经节细胞神经保护作用。玻璃体内注射血小板衍生生长因子 -AA 或 -AB 可在实验性升高眼内压后在体内引起明显的视神经神经保护作用。这些数据表明间质干细胞分泌多种神经营养蛋白,并提示血小板衍生生长因子的分泌尤其可能在间质干细胞介导的视网膜神经节细胞神经保护中发挥重要作用。此外,血小板衍生生长因子可能代表实现视网膜神经节细胞神经保护的独立靶标。
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