Yang F, Feng L, Zheng F, Johnson S W, Du J, Shen L, Wu C P, Lu B
Institute of Neuroscience, Chinese Academy of Sciences, Shanghai, China 200031.
Nat Neurosci. 2001 Nov;4(11):1071-8. doi: 10.1038/nn734.
Glial cell line-derived neurotrophic factor (GDNF) prevents lesion-induced death of midbrain dopaminergic neurons, but its function in normal brain remains uncertain. Here we show that GDNF acutely and reversibly potentiated the excitability of cultured midbrain neurons by inhibiting transient A-type K(+) channels. The effects of GDNF were limited to large, tyrosine hydroxylase (TH)-positive dopaminergic neurons, and were mediated by mitogen associated protein (MAP) kinase. Application of GDNF also elicited a MAP kinase-dependent enhancement of the excitability in dopaminergic neurons in midbrain slice. These results demonstrate an acute regulation of GDNF on ion channels and its underlying signaling mechanism, and reveal an unexpected role of GDNF in normal midbrain dopaminergic neurons.
胶质细胞系源性神经营养因子(GDNF)可防止损伤诱导的中脑多巴胺能神经元死亡,但其在正常大脑中的功能仍不确定。在此我们表明,GDNF通过抑制瞬时A型钾通道,急性且可逆地增强培养的中脑神经元的兴奋性。GDNF的作用仅限于大型酪氨酸羟化酶(TH)阳性多巴胺能神经元,并由丝裂原相关蛋白(MAP)激酶介导。应用GDNF还可引起中脑切片中多巴胺能神经元兴奋性的MAP激酶依赖性增强。这些结果证明了GDNF对离子通道的急性调节及其潜在信号机制,并揭示了GDNF在正常中脑多巴胺能神经元中的意外作用。