Yu Albert Cheung Hoi, Liu Rong Yu, Zhang Yun, Sun Hao Rui, Qin Lu Ye, Lau Lok Ting, Wu Bing Yi, Hui Hung Kit, Heung Man Yeung, Han Ji Sheng
Neuroscience Research Institute, Peking University, Beijing, China.
J Neurosci Res. 2007 Nov 15;85(15):3457-64. doi: 10.1002/jnr.21345.
Glial cell line-derived neurotrophic factor (GDNF) promotes the survival and functions of neurons. It has been shown to be a promising candidate in the treatment of ischemia and other neurodegenerative diseases. We transfected mouse astrocytes in primary cultures with a human GDNF gene and found that their conditioned medium could not only support the growth and survival of cultured dopaminergic neurons but also protect astrocytes from staurosporine- and ischemia-induced apoptosis. This indicated that these transfected astrocytes could release GDNF. A similar protective effect on astrocytes against apoptosis was evident when recombinant human GDNF was used. Moreover, GDNF reduced caspase-3 activity but not that of caspase-1 in cultured astrocytes after ischemia treatment. Thus, GDNF protects astrocytes from apoptosis by inhibiting the activation of caspase-3.
胶质细胞系源性神经营养因子(GDNF)可促进神经元的存活和功能。它已被证明是治疗缺血及其他神经退行性疾病的一个有前景的候选药物。我们用人类GDNF基因转染原代培养的小鼠星形胶质细胞,发现其条件培养基不仅能支持培养的多巴胺能神经元的生长和存活,还能保护星形胶质细胞免受星形孢菌素和缺血诱导的凋亡。这表明这些转染的星形胶质细胞能够释放GDNF。当使用重组人GDNF时,对星形胶质细胞抗凋亡有类似的保护作用。此外,缺血处理后,GDNF降低了培养的星形胶质细胞中caspase-3的活性,但未降低caspase-1的活性。因此,GDNF通过抑制caspase-3 的激活来保护星形胶质细胞免受凋亡。