14-3-3 gamma and zeta protein expression in active microglia Immune response mechanisms of Parkinson’s disease

作     者：Jing He Shenggang Sun Xiaowu Chen 

作者机构：Department of Neurology the Third Hospital of Wuhan Wuhan 430060 Hubei Province China Department of Neurolog-y the Affiliated Union Hospital of Tongji Medical College Huazhong University of Science and Technology Wuhan410128 Hubei Province China 

出 版 物：《Neural Regeneration Research》 (中国神经再生研究（英文版）)

年 卷 期：2008年第3卷第3期

页      面：233-236页

核心收录：

学科分类：0710[理学-生物学] 1002[医学-临床医学] 1001[医学-基础医学(可授医学、理学学位)] 100204[医学-神经病学] 10[医学] 

主　　题：14-3-3 protein microglia lipopolysaccharide TNF-α 

摘      要：BACKGROUND： The progressive degeneration of dopaminergic neurons in Parkinson＇s disease is associated with an activated glial reaction, combined with an inflammatory process. These responses lead to the production of cytokines, such as interferon- γ, tumor necrosis factor- α （TNF- α ）, and interleukin-1 β. In addition, 14-3-3 protein is a component of Lewy bodies in Parkinson＇s disease. OBJECTIVE： To observe the expression of 14-3-3 γ and ζ protein, as well as TNF-α, in mouse microglia, as well as changes after lipopolysaccharide （LPS） activation. To investigate possible mechanisms of dopaminergic neuronal injury due to activated microglia. To and clarify the immune response mechanisms of Parkinson＇s disease. DESIGN： Randomized controlled observation, cell study. SETTING： Laboratory of Department of Neurology, the Affiliated Union Hospital of Tongji Medical College, Huazhong University of Science and Technology. MATERIALS： The BV-2 immortalized murine microglia cell line was purchased from China Unit cell center. LPS was provided by Sigma Company. Cell cultures were purchased from Gibco. Phospho-（Ser） 14-3-3 binding motif antibody was purchased from Santa Cruz Biotechnologies. FITC was provided by Linfei Biotechnology, Wuhan, China. TNF- α ELISA was provided by Jingmei Biotech Co, Wuhan, China. The flow cytometer was provided by Becton Dickinson, Canada. METHODS： The present experiment was performed at the Laboratory of Department of Neurology, the Affiliated Union Hospital of Tongji Medical College, Huazhong University of Science and Technology from April to December 2006. The microglial cell line, BV-2, was cultured in vitro and stimulated with LPS for 2, 6, 12, and 24 hours. BV-2 cultures without LPS were used as controls. MAIN OUTCOME MEASURES： Expression of 14-3-3 γ protein was detected by flow cytometry. 14-3-3 ζ percentage expression and the mean fluorescence intensity was detected by immunofluorescence. TNF- α expression was detected by ELISA. RES