Lee Young Sook, Kang Joon Won, Lee Young Ho, Kim Dong Woon
Department of Anatomy, School of Medicine, Chungnam National University, Daejeon, Korea.
Anat Cell Biol. 2011 Jun;44(2):128-34. doi: 10.5115/acb.2011.44.2.128. Epub 2011 Jun 30.
Inhibitor of DNA binding (ID) proteins bind to and inhibit the function of basic helix-loop-helix transcription factors, including those that regulate proliferation and differentiation during development. However, little is known about the role of ID proteins in glial activation under neuropathological conditions. In this study, we evaluated the expression of ID4 following induction of excitotoxic lesions in mouse brain by kainic acid injection. The number of ID4-expressing astrocytes increased in the CA1 layer of the injured hippocampus until 3 days post-lesion. To analyze the effects of ID4 on cell proliferation, primary astrocytes were transduced with recombinant adenovirus expressing GFP-ID4. Overexpression of ID4 led to increased proliferation of astrocytes. These results suggest that ID4 plays a proliferative role in astrocyte activation after excitotoxin-induced hippocampal neuronal death.
DNA结合抑制因子(ID)蛋白与碱性螺旋-环-螺旋转录因子结合并抑制其功能,这些转录因子包括在发育过程中调节增殖和分化的因子。然而,关于ID蛋白在神经病理条件下神经胶质细胞激活中的作用知之甚少。在本研究中,我们通过注射海藻酸诱导小鼠脑内兴奋性毒性损伤,评估ID4的表达。在损伤后3天内,损伤海马体CA1层中表达ID4的星形胶质细胞数量增加。为了分析ID4对细胞增殖的影响,用表达GFP-ID4的重组腺病毒转导原代星形胶质细胞。ID4的过表达导致星形胶质细胞增殖增加。这些结果表明,ID4在兴奋性毒素诱导的海马神经元死亡后星形胶质细胞激活中起增殖作用。