The Function of ASK1 in Sepsis and Stress-Induced Disorders

被引:0
|
作者
Kostyak, John C. [1 ]
Mckenzie, Steven E.
Naik, Ulhas P. [1 ]
Barbieri, Silvia S.
机构
[1] Thomas Jefferson Univ, Cardeza Fdn Hematol Res, Cardeza Ctr Hemostasis Thrombosis & Vasc Biol, Dept Med,Sidney Kimmel Med Coll, Philadelphia, PA 19107 USA
基金
美国国家卫生研究院;
关键词
sepsis; ASK1; stress; platelet; FC-GAMMA-RIIA; HEPARIN-INDUCED THROMBOCYTOPENIA; INDUCED PLATELET ACTIVATION; KINASE; ASK1; PROTEIN-KINASE; STAPHYLOCOCCUS-AUREUS; DEPENDENT ACTIVATION; COLLAGEN RECEPTOR; GLYCOPROTEIN-VI; HOST-DEFENSE;
D O I
10.3390/ijms25010213
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 signal-regulating kinase 1 (ASK1) is a serine-threonine kinase that is ubiquitously expressed in nucleated cells and is responsible for the activation of multiple mitogen-activated protein kinases (MAPK) to regulate cell stress. Activation of ASK1 via cellular stress leads to activation of downstream signaling components, activation of transcription factors, and proinflammatory cytokine production. ASK1 is also expressed in anucleate platelets and is a key player in platelet activation as it is important for signaling. Interestingly, the mechanism of ASK1 activation is cell type-dependent. In this review we will explore how ASK1 regulates a variety of cellular processes from innate immune function to thrombosis and hemostasis. We will discuss how ASK1 influences Fc gamma RIIA-mediated platelet reactivity and how that reactivity drives platelet clearance. Furthermore, we will explore the role of ASK1 in thromboxane (TxA2) generation, which highlights differences in the way ASK1 functions in mouse and human platelets.
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页数:13
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