Mechanisms of Hepatic toxicity III. Intracellular signaling in response to toxic liver injury

被引:35
作者
Jones, BE
Czaja, MJ
机构
[1] Yeshiva Univ Albert Einstein Coll Med, Marion Bessin Liver Res Ctr, Bronx, NY 10461 USA
[2] Yeshiva Univ Albert Einstein Coll Med, Dept Med, Bronx, NY 10461 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY | 1998年 / 275卷 / 05期
关键词
mitogen-activated protein kinase; ceramide; nitric oxide; activator protein-1; c-Myc; nuclear factor-kappa B; Fas;
D O I
10.1152/ajpgi.1998.275.5.G874
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Toxin-induced liver injury was formerly considered a passive biochemical event, but recent evidence has demonstrated that signal transduction pathways actively modulate the hepatocyte's response to this form of injury. Investigations have examined the effects of a variety of toxins on the activation of receptor-coupled signal transduction, mitogen-activated protein kinases, and Fas signaling, as well as the generation of second messengers such as ceramide and nitric oxide. Many of these pathways culminate in the activation of transcription factors such as activator protein-1, c-Myc, or nuclear factor-kappa B. This Themes article discusses the effects of toxic injury on these signaling pathways and their known functions in regulating hepatocyte death and proliferation following injury.
引用
收藏
页码:G874 / G878
页数:5
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