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巨噬细胞的激活诱导死亡
引用本文:韦锦学,顾军.巨噬细胞的激活诱导死亡[J].生命科学,2006,18(2):180-182.
作者姓名:韦锦学  顾军
作者单位:北京大学生命科学学院,蛋白质工程与植物基因工程国家重点实验室,北京,100871
基金项目:国家自然科学基金资助项目(30330260)
摘    要:淋巴细胞的激活诱导细胞死亡(AICD)的分子机制已经得到了广泛的研究。巨噬细胞中也存在AICD,但是诱导巨噬细胞AICD的分子机理仍不是很清楚。最近,一些研究表明zVAD或IFNγ通过提高MEF2C蛋白稳定性,从而增加其在巨噬细胞中的含量。MEF2C和TLR2、4信号通路一起,诱导了Nur77的表达。Nur77的表达介导了巨噬细胞的凋亡。LPS激活的ERK和p38是诱导Nur77表达和细胞凋亡所必需的。p38/STAT1/ROS途径也介导了巨噬细胞的AICD。撤除血清诱导的巨噬细胞凋亡可能是一种新的巨噬细胞AICD模型。这些发现将有助于我们对巨噬细胞AICD的进一步了解。

关 键 词:巨噬细胞  激活诱导死亡  血清撤除  凋亡
文章编号:1004-0374(2006)02-0080-03
收稿时间:2006-01-13
修稿时间:2006-01-16

Activation induced cell death (AICD) in macrophages
WEI Jin-Xue,GU Jun.Activation induced cell death (AICD) in macrophages[J].Chinese Bulletin of Life Sciences,2006,18(2):180-182.
Authors:WEI Jin-Xue  GU Jun
Institution:Laboratory of Protein Engineering and Plant Genetic Engineering, College of Life Sciences, Peiking University, Beijing 100871, China
Abstract:Molecular mechanism of AICD (activation induced cell death) in lymphocytes has been extensively studied. AICD also occurs in macrophages. However, the signaling pathways that are involved in macrophage AICD remains uncertain. Recently, ours and others studies reveal that zVAD or IFN induces the increase of MEF2C protein, possibly by increasing its protein stability. MEF2C, together with TLR2 and TLR4 signaling, induces Nur77 expression leading macrophage to death. LPS- activated ERK and p38 also mediate Nur77 expression. p38/STAT1/ROS pathway contribute to AICD of macrophage as well. Serum-deprivation induced macrophage apoptosis is identified as one kind of macrophage's AICD. These finding will help to better understand the mechanism of AICD in macrophages.
Keywords:macrophages  activation induced cell death  serum deprivation  apoptosis
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