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叉头转录因子在脑缺血中的病理生理学相关性。

Pathophysiological relevance of forkhead transcription factors in brain ischemia.

机构信息

Department of Pharmacology, Graduate School of Pharmaceutical Sciences, 21st Century COE program CRESCENDO, Tohoku University, Aramaki-Aoba, Aoba-ku, Sendai 980-8578, Japan.

出版信息

Adv Exp Med Biol. 2009;665:130-42. doi: 10.1007/978-1-4419-1599-3_10.

Abstract

Forkhead box transcription factor, class 0 (FOXO) is a mammalian homologue of DAF-16, which is known to regulate the lifespan of Caenorhabditis elegans and includes subfamiies of forkhead transcription factors such as FOXO1 (FKHR). FOXO3 (FKHRL1), FOXO4 (AFX) and FOXO6. All these FOXO members are expressed in the brain with different spatial patterns. FOXO1 is phosphorylated on three sites (Thr-24, Ser-256 and Ser-319) in phosphatidylinositol 3-kinase (PI3-K)/Akt-dependenr manner, thereby inhibiting apoptosis signals. We here documented dephosphorylation of FOXO1, FOXO3 and FOXO4 following transient forebrain ischemia with its concomitant translocation into the nucleus in neurons in the gerbil and mouse brains. The dephosphorylarion of FOXO1 following brain ischemia is in part mediated by constirutively active calcineurin in the mouse hippocampus. The activation of FOXOs preceded delayed neuronal death in the vulnerable hippocampal regions following ischemic brain injury. The FOXOl activation is accompanied by an increase in DNA binding activity for FOXO1-responsive element on the Fas ligand promoter. Thus, downstream targets induced by FOXOl include Fas ligand and Bcl-2-interacting mediator of cell death (Bim) in the brain ischemia. Accumulating evidence documented how FOXO activation is involved in the mechanisms of ischemic cell death. In this chapter, we document the activation mechanism of FOXO factors following brain ischemia and deline their downstream targets underlying neuronal death. The pathophysiological relevance of crosstalk between FOXOs and calcineurmn pathways is also discussed. Finally, we propose therapeutic perspectives to rescue neurons from delayed neuronal death by promoting the Akt signaling. Vanadium compounds, protein tyrosine phosphatase inhibitor, up-regulates Akt activity in the brain and thereby rescues neurons from delayed neuronal death by inhibiting FOXO-dependent and -independent death signals in neurons.

摘要

叉头框转录因子 0 类(FOXO)是哺乳动物 DAF-16 的同源物,已知其调节秀丽隐杆线虫的寿命,并包括叉头转录因子亚家族,如 FOXO1(FKHR)、FOXO3(FKHRL1)、FOXO4(AFX)和 FOXO6。所有这些 FOXO 成员都在大脑中表达,具有不同的空间模式。FOXO1 在磷脂酰肌醇 3-激酶(PI3-K)/Akt 依赖性方式下在三个位点(Thr-24、Ser-256 和 Ser-319)磷酸化,从而抑制凋亡信号。我们在这里记录了短暂性前脑缺血后 FOXO1、FOXO3 和 FOXO4 的去磷酸化,以及其在沙鼠和小鼠大脑神经元中的核转位。小鼠海马中的组成性激活钙调神经磷酸酶部分介导了脑缺血后 FOXO1 的去磷酸化。FOXO 的激活先于缺血性脑损伤后易损海马区的迟发性神经元死亡。FOXO1 的激活伴随着 Fas 配体启动子上 FOXO1 反应元件的 DNA 结合活性增加。因此,FOXO1 诱导的下游靶标包括脑缺血中的 Fas 配体和 Bcl-2 相互作用的细胞死亡介体(Bim)。越来越多的证据表明,FOXO 激活参与了缺血性细胞死亡的机制。在这一章中,我们记录了脑缺血后 FOXO 因子的激活机制,并描述了其下游靶标在神经元死亡中的作用。还讨论了 FOXO 和钙调神经磷酸酶途径之间的串扰的病理生理相关性。最后,我们提出了通过促进 Akt 信号转导来挽救神经元免受迟发性神经元死亡的治疗观点。钒化合物、蛋白酪氨酸磷酸酶抑制剂,通过抑制神经元中 FOXO 依赖性和非依赖性死亡信号,增加大脑中的 Akt 活性,从而挽救神经元免受迟发性神经元死亡。

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