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κB激酶β(IKKβ/IKK2/IKBKB)——转录因子NF-κB信号传导中的关键分子。

IkappaB kinase beta (IKKbeta/IKK2/IKBKB)--a key molecule in signaling to the transcription factor NF-kappaB.

作者信息

Schmid Johannes A, Birbach Andreas

机构信息

Center for Biomolecular Medicine and Pharmacology, Medical University Vienna, Austria.

出版信息

Cytokine Growth Factor Rev. 2008 Apr;19(2):157-65. doi: 10.1016/j.cytogfr.2008.01.006. Epub 2008 Mar 4.

Abstract

IKKbeta/IKBKB (IkappaB kinase beta), also designated as IKK2, was named after its function of phosphorylating IkappaB molecules, the inhibitors of NF-kappaB transcription factors. The kinase activity of IKKbeta targets two adjacent serine residues of IkappaB leading to ubiquitination and proteasomal degradation of the inhibitor, followed by release and activation of NF-kappaB. Many signaling pathways that activate NF-kappaB converge at the level of IKKbeta. Examples of stimuli leading to IKKbeta and subsequent NF-kappaB activation include inflammatory cytokines (IL-1, TNFalpha), endotoxins (lipopolysaccharide), viral infection and double strand RNA as well as physical signals such as UV-irradiation. Transcription factors of the NF-kappaB protein family have a great variety of functions in regulating the immune system, cellular differentiation, survival and proliferation. NF-kappaB is an essential factor in acute as well as chronic inflammation, a pathological state which is either cause or co-factor in a great variety of diseases. Moreover, recent data suggest that many variants of cancer are characterized by elevated constitutive activity of NF-kappaB, which can act as a survival factor for malignant cells by its predominantly anti-apoptotic function. Given the tight regulation of NF-kappaB by IkappaB molecules and the central role of IKKbeta in phosphorylation and degradation of the inhibitor, IKKbeta is a very promising target for pharmaceutical substances aiming at interfering with NF-kappaB activation.

摘要

IKKβ/IKBKB(核因子κB抑制蛋白激酶β),也被称为IKK2,因其具有磷酸化核因子κB转录因子抑制剂IkappaB分子的功能而得名。IKKβ的激酶活性作用于IkappaB的两个相邻丝氨酸残基,导致该抑制剂发生泛素化并经蛋白酶体降解,随后核因子κB被释放并激活。许多激活核因子κB的信号通路在IKKβ水平汇聚。导致IKKβ及随后核因子κB激活的刺激因素包括炎性细胞因子(白细胞介素-1、肿瘤坏死因子α)、内毒素(脂多糖)、病毒感染和双链RNA,以及诸如紫外线照射等物理信号。核因子κB蛋白家族的转录因子在调节免疫系统、细胞分化、存活和增殖方面具有多种功能。核因子κB是急性和慢性炎症中的一个重要因素,而炎症这种病理状态在多种疾病中既是病因又是辅助因素。此外,最近的数据表明,许多癌症变体的特征是核因子κB的组成型活性升高,它可通过其主要的抗凋亡功能充当恶性细胞的存活因子。鉴于IkappaB分子对核因子κB的严格调控以及IKKβ在抑制剂磷酸化和降解中的核心作用,IKKβ是旨在干扰核因子κB激活的药物非常有前景的靶点。

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