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核因子κB调控网络。

The NF-kappaB regulatory network.

作者信息

Brasier Allan R

机构信息

Department of Internal Medicine and Sealy Center for Molecular Sciences, University of Texas Medical Branch, Galveston, TX 77555-1060, USA.

出版信息

Cardiovasc Toxicol. 2006;6(2):111-30. doi: 10.1385/ct:6:2:111.

Abstract

Nuclear factor (NF)-kappaB is a family of seven structurally related transcription factors that play a central role in cardiovascular growth, stress response, and inflammation by controlling gene network expression. Although the NF- kappaB subunits are ubiquitously expressed, their actions are regulated in a celltype and stimulus-specific manner, allowing for a diverse spectrum of effects. For example, NF-kappalB is activated by cytokines, reactive oxygen species, bacterial cell wall products, vasopressors, viral infection, and DNA damage. Recent molecular dissection of its mechanisms for activation has shown that NF-kappalB can be induced by the so-called "canonical" and "noncanonical" pathways, leading to distinct patterns in the individual subunits activated and downstream genetic responses produced. The canonical pathway involves activating the IkappalB kinase (IKK) with subsequent phosphorylation-induced proteolysis of the IkappaBalpha inhibitors and consequent nuclear translocation of the Rel A transcriptional activator. Recent work using high-density oligonucleotide arrays have begun to systematically dissect the scope of the gene network under canonical NF-kappaB control and have yielded important insights into biological pathways controlled by it. This pathway controls expression of noncontiguous, functionally discrete groups of genes ("regulons"), whose temporal expression occurs in waves. Moreover, its mode of activation (oscillatory or monophasic) plays an important role in determining the spectrum of target genes expressed. By contrast, the noncanonical NF-kappaB activation pathway involves activating the NF-kappaB inducing kinase (NIK) to stimulate IKKalpha-induced phosphorylation and proteolytic processing of the 100-kDa cytoplasmic NF-kappaB2 precursor. Activated NF-kappaB2 then forms a complex with Rel B and NIK to translocate into the nucleus thereby activating a distinct set of genes. Although the noncanonical pathway has been most clearly linked to control of adaptive immunity, recent intriguing studies have implicated this pathway in viral induced stress response and in the metabolic syndrome. In this way, a single family of transcription factors can respond to diverse stimuli to regulate cardiovascular homeostasis.

摘要

核因子(NF)-κB是由七个结构相关的转录因子组成的家族,通过控制基因网络表达在心血管生长、应激反应和炎症中发挥核心作用。尽管NF-κB亚基在全身广泛表达,但其作用是以细胞类型和刺激特异性的方式进行调节的,从而产生多种多样的效应。例如,NF-κB可被细胞因子、活性氧、细菌细胞壁产物、血管加压素、病毒感染和DNA损伤激活。最近对其激活机制的分子剖析表明,NF-κB可由所谓的“经典”和“非经典”途径诱导,导致激活的单个亚基和产生的下游基因反应出现不同模式。经典途径涉及激活IκB激酶(IKK),随后通过磷酸化诱导IκBα抑制剂的蛋白水解,并导致Rel A转录激活因子的核转位。最近使用高密度寡核苷酸阵列的研究已开始系统地剖析经典NF-κB控制下的基因网络范围,并对其控制的生物学途径有了重要的认识。该途径控制非连续的、功能上离散的基因群(“调节子”)的表达,其时间表达呈波浪状。此外,其激活模式(振荡或单相)在决定表达的靶基因谱方面起着重要作用。相比之下,非经典NF-κB激活途径涉及激活NF-κB诱导激酶(NIK),以刺激IKKα诱导的100 kDa细胞质NF-κB2前体的磷酸化和蛋白水解加工。激活的NF-κB2然后与Rel B和NIK形成复合物转位到细胞核中,从而激活一组不同的基因。尽管非经典途径与适应性免疫的控制联系最为明确,但最近有趣的研究表明该途径与病毒诱导的应激反应和代谢综合征有关。通过这种方式,一个转录因子家族可以对多种刺激做出反应,以调节心血管稳态。

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