Karin Michael
Laboratory of Gene Regulation and Signal Transduction, Department of Pharmacology, School of Medicine, University of California San Diego, La Jolla, California 92093, USA.
J Clin Invest. 2006 Nov;116(11):2866-8. doi: 10.1172/JCI30268.
Activation of transcription factor NF-kappaB, the major regulator of the inflammatory response, depends on the inhibitor of NF-kappaB kinase (IKK) complex, which is composed of 2 catalytic subunits, IKK1 and IKK2 (also known as IKKalpha and IKKbeta), and a regulatory subunit, IKKgamma (also known as NEMO). In this issue of the JCI, Mourkioti et al. show that muscle-specific disruption in mice of the gene encoding IKK2 prevents NF-kappaB activation in response to denervation or toxin-induced injury (see the related article beginning on page 2945). Importantly, this genetic manipulation prevents muscle wasting, thereby providing strong evidence in support of a major pathogenic role for inflammation in a variety of muscular dystrophies characterized by progressive muscle fiber degeneration.
转录因子NF-κB是炎症反应的主要调节因子,其激活依赖于NF-κB激酶(IKK)复合物的抑制剂,该复合物由2个催化亚基IKK1和IKK2(也称为IKKα和IKKβ)以及1个调节亚基IKKγ(也称为NEMO)组成。在本期《临床研究杂志》中,穆尔基奥蒂等人表明,在小鼠中对编码IKK2的基因进行肌肉特异性破坏可防止因去神经支配或毒素诱导的损伤而导致的NF-κB激活(见第2945页开始的相关文章)。重要的是,这种基因操作可防止肌肉萎缩,从而为炎症在多种以进行性肌纤维退化为特征的肌肉营养不良症中的主要致病作用提供了有力证据。