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小鼠海马体兴奋性毒性损伤后星形胶质细胞中生长分化因子15的表达

Growth Differentiation Factor 15 Expression in Astrocytes After Excitotoxic Lesion in the Mouse Hippocampus.

作者信息

Yi Min-Hee, Zhang Enji, Baek Hyunjung, Kim Sena, Shin Nara, Kang Joon Won, Lee Sunyeul, Oh Sang-Ha, Kim Dong Woon

机构信息

Department of Anatomy, Brain Research Institute, Chungnam National University School of Medicine, Daejeon 301-747, Korea.

Department of Anatomy, Brain Research Institute, Chungnam National University School of Medicine, Daejeon 301-747, Korea. ; Department of Pediatrics, Chungnam National University Hospital, Daejeon 301-721, Korea.

出版信息

Exp Neurobiol. 2015 Jun;24(2):133-8. doi: 10.5607/en.2015.24.2.133. Epub 2015 Mar 30.

Abstract

Growth differentiation factor 15 (GDF15) is, a member of the transforming growth factor β (TGF-β) superfamily of proteins. Although GDF15 is well established as a potent neurotrophic factor for neurons, little is known about its role in glial cells under neuropathological conditions. We monitored GDF15 expression in astrocyte activation after a kainic acid (KA)-induced neurodegeneration in the ICR mice hippocampus. In control, GDF15 immunoreactivity (IR) was evident in the neuronal layer of the hippocampus; however, GDF15 expression had increased in activated astrocytes throughout the hippocampal region at day 3 after the treatment with KA. LPS treatment in astrocytes dramatically increased GDF15 expression in primary astrocytes. In addition, LPS treatment resulted in the decrease of the IκB-α degradation and increase of the phosphorylation level of RelA/p65. These results indicate that GDF15 has a potential link to NF-κB activation, making GDF15 a valuable target for modulating inflammatory conditions.

摘要

生长分化因子15(GDF15)是转化生长因子β(TGF-β)超家族蛋白的成员。尽管GDF15作为一种对神经元有效的神经营养因子已被充分证实,但在神经病理条件下其在神经胶质细胞中的作用却知之甚少。我们监测了海人酸(KA)诱导的ICR小鼠海马神经变性后星形胶质细胞激活过程中GDF15的表达。在对照组中,GDF15免疫反应性(IR)在海马的神经元层中明显可见;然而,在用KA处理后第3天,整个海马区域激活的星形胶质细胞中GDF15表达增加。星形胶质细胞中的脂多糖(LPS)处理显著增加了原代星形胶质细胞中GDF15的表达。此外,LPS处理导致IκB-α降解减少和RelA/p65磷酸化水平增加。这些结果表明GDF15与NF-κB激活存在潜在联系,使GDF15成为调节炎症状态的一个有价值的靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/17f8/4479809/406c38fb4a35/en-24-133-g001.jpg

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