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Pigment epithelium-derived factor acts as an opponent of growth-stimulatory factors in retinal glial-endothelial cell interactions

机译:色素上皮衍生因子在视网膜胶质-内皮细胞相互作用中充当生长刺激因子的对手

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摘要

Pigment epithelium-derived factor (PEDF), a glycoprotein with pleiotropic functions, is naturally occuring in the eye and considered as crucial to prevent pathological angiogenesis. Since retinal glial (Muller) cells produce PEDF, the authors have studied its impact on glial-endothelial cellular interactions. Bovine retinal endothelial cells were cultured in the presence of culture media originating from primary Muller cells, and endothelial proliferation as well as phosphorylation of the mitogen-activated protein kinases extracellular signal-regulated kinases (ERK)-1/-2 were investigated. The concerted activity of Muller-cell derived soluble mediators attenuated endothelial proliferation and ERK-1/-2 activation, regardless of whether the Muller cells were preincubated under normoxia or hypoxia, and even though the endothelial cells were stimulated by vascular endothelial growth factor-A (VEGF). This inhibitory activity was no longer demonstrable if high levels of basic fibroblast growth factor or VEGF were supplied, suggesting that in cases of pathological neovascularization, overproduction of proangiogenic mediators overrides the "antiangiogenic background" provided by Muller cells. However, neutralizing the activity of PEDF partially restored endothelial cell proliferation and resulted in increased ERK-1/-2 activation, which is in concordance with findings demonstrating that exogenously applied PEDF is able to suppress VEGF-induced ERK-1/-2 phosphorylation. PEDF production by Muller cells is not only regulated by retinal oxygen but also by the activity of soluble factors released from retinal endothelial cells. For instance, PEDF levels were significantly elevated in glial (Muller)-endothelial cell cocultures as compared with bovine retinal endothelial cell-free Muller cell cultures. These results have implications for the pathogenesis of retinal neovascularization since the Muller cell may be regarded as a central control element which modulates retinal PEDF levels and, thus, is of critical importance for adjusting the balance between proangiogenic and antiangiogenic mediators. (c) 2007 Wiley-Liss, Inc.
机译:色素上皮衍生因子(PEDF)是一种具有多效功能的糖蛋白,在眼中自然存在,被认为对于预防病理性血管生成至关重要。由于视网膜神经胶质(Muller)细胞产生PEDF,因此作者研究了其对神经胶质-内皮细胞相互作用的影响。在原代Muller细胞来源的培养基存在下培养牛视网膜内皮细胞,并研究内皮细胞的增殖以及丝裂原活化蛋白激酶的磷酸化,胞外信号调节激酶(ERK)-1 / -2。 Muller细胞来源的可溶性介体的协同活性减弱了内皮细胞的增殖和ERK-1 / -2激活,无论Muller细胞是在常氧还是低氧条件下进行预培养,即使内皮细胞是由血管内皮生长因子A刺激的(VEGF)。如果提供高水平的碱性成纤维细胞生长因子或VEGF,则这种抑制活性将不再显示出来,这表明在病理性新血管形成的情况下,促血管生成介质的过度产生将覆盖Muller细胞提供的“抗血管生成背景”。但是,中和PEDF的活性可部分恢复内皮细胞的增殖,并导致ERK-1 / -2活化增加,这与证明外源应用PEDF能够抑制VEGF诱导的ERK-1 / -2磷酸化的发现一致。穆勒细胞产生的PEDF不仅受视网膜氧的调节,而且还受视网膜内皮细胞释放的可溶性因子活性的调节。例如,与无牛视网膜内皮细胞的Muller细胞培养物相比,在胶质(Muller)-内皮细胞共培养物中PEDF水平显着升高。这些结果对视网膜新血管形成的发病机制具有影响,因为穆勒细胞可以被认为是调节视网膜PEDF水平的中央控制元件,因此对于调节促血管生成和抗血管生成介质之间的平衡至关重要。 (c)2007年Wiley-Liss,Inc.

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