Serum deprivation induced apoptosis in macrophage is mediated by autocrine secretion of type IIFNs

被引:17
作者
Wei, J [1 ]
Sun, Z [1 ]
Chen, Q [1 ]
Gu, J [1 ]
机构
[1] Peking Univ, Coll Life Sci, Natl Key Lab Prot Engn & Plant Genet Engn, Beijing 100871, Peoples R China
基金
美国国家科学基金会;
关键词
apoptosis; autocrine secretion; IFNs; serum deprivation;
D O I
10.1007/s10495-006-5146-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Apoptosis can be triggered by different forms of cellular stress. We here show that serum deprivation induces the expression and secretion of type I interferons and results in apoptosis in RAW 264.7 cell in a caspase dependent manner. Administration of either IFN-alpha or IFN-beta antibody partially inhibits apoptosis while the two antibodies used together totally prevents RAW264.7 cell from apoptosis. GM-CSF, but not M-CSF and IL-3, protects serum deprivation induced apoptosis. Inhibition of JAKs also prevents macrophages from apoptosis. Activation of MAPKs is not required for serum deprivation induced apoptosis. Our results are the first to demonstrate that serum deprivation-induced apoptosis acts through autocrine secretion of type I interferons.
引用
收藏
页码:545 / 554
页数:10
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