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色素上皮衍生因子可保护培养的小脑颗粒细胞免受谷氨酸诱导的神经毒性。

Pigment epithelium-derived factor protects cultured cerebellar granule cells against glutamate-induced neurotoxicity.

作者信息

Taniwaki T, Hirashima N, Becerra S P, Chader G J, Etcheberrigaray R, Schwartz J P

机构信息

Clinical Neuroscience Branch, National Institute of Neurological Disorders and Stroke, NIH, Bethesda, Maryland 20892-1279, USA.

出版信息

J Neurochem. 1997 Jan;68(1):26-32. doi: 10.1046/j.1471-4159.1997.68010026.x.

Abstract

Pigment epithelium-derived factor (PEDF) is a survival factor for cerebellar granule cells in culture. In the present study, we have investigated the ability of a recombinant form of PEDF (rPEDF) to protect against glutamate neurotoxicity. When rPEDF was added to cerebellar granule cell cultures 30 min before addition of 100 microM glutamate, glutamate-induced neuronal death was significantly reduced. The protective effect of rPEDF was dose-dependent in the range from 0.023 to 7.0 nM (1-500 ng/ml), with a half-maximal dose of 0.47 nM. An antibody to rPEDF blocked this protective effect. Measurement of intraneuronal free calcium levels demonstrated that rPEDF raised the basal calcium content. However, after the elevation of intracellular calcium in response to administration of glutamate, rPEDF reduced the plateau level seen in the presence of glutamate. These data show that PEDF can protect neurons against glutamate-induced neurotoxicity, possibly via a calcium-related pathway. The finding that only 30 min of preincubation is required for the neuroprotective effect, significantly faster than other known neurotrophic factors, suggests that PEDF may be useful clinically as a neuroprotective agent in the CNS.

摘要

色素上皮衍生因子(PEDF)是培养的小脑颗粒细胞的一种存活因子。在本研究中,我们研究了重组形式的PEDF(rPEDF)抵御谷氨酸神经毒性的能力。在添加100微摩尔谷氨酸之前30分钟将rPEDF添加到小脑颗粒细胞培养物中时,谷氨酸诱导的神经元死亡显著减少。rPEDF的保护作用在0.023至7.0纳摩尔(1至500纳克/毫升)范围内呈剂量依赖性,半数最大剂量为0.47纳摩尔。针对rPEDF的抗体阻断了这种保护作用。对神经元内游离钙水平的测量表明,rPEDF提高了基础钙含量。然而,在因给予谷氨酸而导致细胞内钙升高后,rPEDF降低了在有谷氨酸存在时所见的平台水平。这些数据表明,PEDF可能通过与钙相关的途径保护神经元免受谷氨酸诱导的神经毒性。仅需预孵育30分钟即可产生神经保护作用这一发现,比其他已知的神经营养因子要快得多,表明PEDF在临床上可能作为中枢神经系统中的一种神经保护剂有用。

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