Tsai May-Jywan, Weng Ching-Feng, Shyue Song-Kun, Liou Dann-Ying, Chen Chien-Hung, Chiu Chuan-Wen, Yang Tzu-Hsuan, Pan Hsu-An, Liao Roanna I-Hsin, Kuo Huai-Sheng, Huang Ming-Chao, Huang Wen-Cheng, Hoffer Barry J, Cheng Henrich
Neural Regeneration Laboratory, Neurological Institute, Taipei Veterans General Hospital, Taipei, Taiwan.
J Neurosci Res. 2007 Oct;85(13):2950-9. doi: 10.1002/jnr.21395.
Bone morphogenetic proteins (BMPs), members of the TGF-beta superfamily, have been implicated in nervous system development and in response to injury. Previous studies have shown that recombinant BMP7 can enhance dendritic growth and protect cultured neurons from oxidative stress. Because of the presence of extracellular BMP antagonists, BMP7 seems to act locally. Therefore, the present study uses BMP7 overexpression using adenovirus (Ad)-mediated gene transfer to examine its effect in mixed neuronal cultures. Enhanced BMP7 expression selectively induces neuronal CGRP expression in a time-dependent manner. BMP7 overexpression not only significantly protects cultures from H2O2 toxicity but reduces lipopolysaccharide (LPS) stimulation. Concurrently, it profoundly reduces microglial numbers, but increases oligodendroglial and endothelial cells. Together, low-dose and continuously expressed BMP7 is both neuroprotective and differentiation-inductive.
骨形态发生蛋白(BMPs)是转化生长因子-β超家族的成员,与神经系统发育及损伤反应有关。先前的研究表明,重组BMP7可促进树突生长,并保护培养的神经元免受氧化应激。由于细胞外存在BMP拮抗剂,BMP7似乎在局部发挥作用。因此,本研究使用腺病毒(Ad)介导的基因转移来过表达BMP7,以研究其在混合神经元培养物中的作用。增强的BMP7表达以时间依赖性方式选择性诱导神经元降钙素基因相关肽(CGRP)表达。BMP7过表达不仅能显著保护培养物免受过氧化氢(H2O2)毒性,还能减轻脂多糖(LPS)刺激。同时,它能显著减少小胶质细胞数量,但增加少突胶质细胞和内皮细胞数量。总之,低剂量且持续表达的BMP7具有神经保护和诱导分化的作用。