Islam Omedul, Gong Xiandi, Rose-John Stefan, Heese Klaus
Department of Molecular and Cell Biology, School of Biological Sciences, College of Science, Nanyang Technological University, Singapore, Singapore.
Mol Biol Cell. 2009 Jan;20(1):188-99. doi: 10.1091/mbc.e08-05-0463. Epub 2008 Oct 29.
Besides its wide range of action as a proinflammatory cytokine in the immune system, interleukin-6 (IL-6) has also attracted much attention due to its influence on the nervous system. In the present study we show that the designer fusion protein H-IL-6, consisting of IL-6 and its specific receptor IL-6R-alpha, but not IL-6 alone, mediates both neuro- as well as gliogenesis. Using immunocytochemistry, Western blot, and patch-clamp recording, we demonstrate that H-IL-6 induces the differentiation of neural stem cells (NSCs) specifically into glutamate-responsive neurons and two morphological distinctive astroglia cell types. H-IL-6-activated neurogenesis seems to be induced by the MAPK/CREB (mitogen-activated protein kinase/cAMP response element-binding protein) cascade, whereas gliogenesis is mediated via the STAT-3 (signal transducers and activators of transcription protein-3) signaling pathway. Our finding that IL-6 mediates both processes depending on its specific soluble receptor sIL-6R-alpha has implications for the potential treatment of neurodegenerative diseases.
除了作为免疫系统中一种促炎细胞因子具有广泛作用外,白细胞介素-6(IL-6)因其对神经系统的影响也备受关注。在本研究中,我们发现由IL-6及其特异性受体IL-6R-α组成的设计融合蛋白H-IL-6,而非单独的IL-6,介导神经发生和神经胶质生成。通过免疫细胞化学、蛋白质印迹和膜片钳记录,我们证明H-IL-6可诱导神经干细胞(NSCs)特异性分化为对谷氨酸有反应的神经元以及两种形态不同的星形胶质细胞类型。H-IL-6激活的神经发生似乎是由MAPK/CREB(丝裂原活化蛋白激酶/环磷酸腺苷反应元件结合蛋白)级联反应诱导的,而神经胶质生成则通过STAT-3(信号转导和转录激活因子蛋白-3)信号通路介导。我们发现IL-6根据其特异性可溶性受体sIL-6R-α介导这两个过程,这对神经退行性疾病的潜在治疗具有重要意义。
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