Laboratory of Neuroanatomy and Experimental Neurology, Department of Morphological Sciences, University of Santiago de Compostela, Santiago de Compostela, Spain.
Dev Dyn. 2010 Dec;239(12):3247-59. doi: 10.1002/dvdy.22474.
Reactive oxygen species signaling has been suggested to regulate stem cell development. In the present study, we treated neurospheres of rat mesencephalic precursors with inhibitors of the NADPH oxidase complex and mitochondrial ATP-sensitive potassium (mitoKATP) channel blockers during the proliferation and/or the differentiation periods to study the effects on generation of dopaminergic neurons. Treatment with low doses (100 or 250 μM) of the NADPH inhibitor apocynin during the proliferation period increased the generation of dopaminergic neurons. However, higher doses (1 mM) were necessary during the differentiation period to induce the same effect. Treatment with general (glibenclamide) or mitochondrial (5-hydroxydecanoate) KATP channel blockers during the proliferation and differentiation periods increased the number of dopaminergic neurons. Furthermore, neither increased proliferation rate nor apoptosis had a major role in the observed increase in generation of dopaminergic neurons, which suggests that the redox state is able to regulate differentiation of precursors into dopaminergic neurons.
活性氧信号转导被认为可以调节干细胞的发育。在本研究中,我们在增殖和/或分化期间用 NADPH 氧化酶复合物和线粒体 ATP 敏感性钾 (mitoKATP) 通道抑制剂处理大鼠中脑神经前体细胞的神经球,以研究其对多巴胺能神经元生成的影响。在增殖期用低剂量(100 或 250 μM)NADPH 抑制剂 apocynin 处理可增加多巴胺能神经元的生成。然而,在分化期需要更高的剂量(1 mM)才能诱导相同的效果。在增殖和分化期间用通用(格列本脲)或线粒体(5-羟癸酸)KATP 通道抑制剂处理可增加多巴胺能神经元的数量。此外,观察到多巴胺能神经元生成增加既不是由于增殖率增加也不是由于细胞凋亡增加,这表明氧化还原状态能够调节前体细胞向多巴胺能神经元的分化。