Center for Vascular Biology, Department of Pathology and Laboratory Medicine, Weill Medical College of Cornell University, 1300 York Avenue, New York, NY 10065, USA.
J Clin Invest. 2010 Jan;120(1):90-2. doi: 10.1172/JCI41738. Epub 2009 Dec 28.
Arterial injury results in the formation of neointimal lesions. Lack of resolution of the pathologic neointima leads to stenosis, tissue ischemia, and organ dysfunction. In this issue of the JCI, Kovacic et al. show that, in response to arterial injury in mice, the cytokine TNF-alpha triggers a novel signaling pathway involving the combinatorial action of two transcription factors, STAT3 and NF-kappaB (p65 subunit), in VSMCs (see the related article beginning on page 303). Upon activation, these factors turn on transcription of a potent T cell chemokine, RANTES, which selectively recruits T cells into the vessel wall as part of the vascular wound-healing response.
动脉损伤导致新生内膜病变的形成。病理性新生内膜不能正常消退会导致血管狭窄、组织缺血和器官功能障碍。在本期 JCI 中,Kovacic 等人表明,在小鼠的动脉损伤反应中,细胞因子 TNF-α触发了一个新的信号通路,涉及两种转录因子 STAT3 和 NF-κB(p65 亚基)在血管平滑肌细胞中的协同作用(见第 303 页开始的相关文章)。这些因子被激活后,会开启强效 T 细胞趋化因子 RANTES 的转录,它作为血管愈合反应的一部分将 T 细胞选择性招募到血管壁中。