Activation of signal transducer and activator of transcription 3 in rat liver after heat shock and reperfusion stress

被引:7
作者
Tacchini, L
Fusar-Poli, D
Sironi, M
Mantovani, A
Bernelli-Zazzera, A
机构
[1] Univ Milan, Ist Patol Gen, Ctr Studio Patol Cellulare, CNR, I-20133 Milan, Italy
[2] Ist Ric Farmacol Mario Negri, I-20157 Milan, Italy
关键词
liver; heat shock; ischemia/reperfusion; transcription factors (TFs); cytokines;
D O I
10.1016/S1357-2725(02)00164-4
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
Changes in transcription factors (TFs) accompany many types of cell stresses. By using electrophoretic mobility assays we show that the DNA binding of signal transducer and activator of transcription 3 (STAT3) is activated in rat liver by heat shock and ischemia-reperfusion. Northern blot and Western blot analysis reveal an increase of the mRNA and protein level of this transcription factor. Under both conditions the phosphorylation of pre-existing STAT3 is prompt and precedes the increase in the STAT3 protein. The activation: (1) is functional, i.e. is followed by the transcription of the target gene at-acid glycoprotein (2) is strongly inhibited by pretreatment with the interleukin-1 receptor antagonist before heat shock but only slightly by pretreatment before ischemia-reperfusion (3) might, at least in part, be mediated by a cytokine cascade involving also interleukin-6. These results are consistent with the hypothesis that different kinds of stress can activate a number of common TFs. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:316 / 323
页数:8
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