Kitasato Institute for Life Sciences, Kitasato University, Tokyo, Japan.
Curr Mol Med. 2010 Apr;10(3):259-66. doi: 10.2174/156652410791065354.
Neuronal degeneration is closely associated with cognitive, motor and visual dysfunctions. Neuroprotective strategies have been investigated with the view to being employed as potential therapy for patients with these disabilities. Pigment epithelium-derived factor (PEDF) is a 50-kDa secreted glycoprotein and a non-inhibitory member of the serine protease inhibitor (SERPIN) gene family. PEDF is detected in a broad range of human tissues, including almost all brain areas, and has been shown to have strong neuroprotective properties for various types of neurons including cerebellar granule neurons, hippocampal neurons, striatal neurons, retinal neurons and spinal cord motor neurons. These observations raise the possibility that application of PEDF may be helpful in designing new therapeutic strategies for neurodegenerative diseases such as amyotrophic lateral sclerosis, Parkinson's disease, Huntington's disease, Alzheimer's disease and brain ischemia.
神经元变性与认知、运动和视觉功能障碍密切相关。人们研究了神经保护策略,以期将其作为这些残疾患者的潜在治疗方法。色素上皮衍生因子(PEDF)是一种 50kDa 的分泌糖蛋白,是非丝氨酸蛋白酶抑制剂(SERPIN)基因家族的无抑制成员。PEDF 在广泛的人体组织中被检测到,包括几乎所有的大脑区域,并已显示出对各种类型的神经元具有强大的神经保护作用,包括小脑颗粒神经元、海马神经元、纹状体神经元、视网膜神经元和脊髓运动神经元。这些观察结果提出了这样一种可能性,即应用 PEDF 可能有助于设计治疗肌萎缩侧索硬化症、帕金森病、亨廷顿病、阿尔茨海默病和脑缺血等神经退行性疾病的新治疗策略。