Williams Julie M, Pettitt Trevor R, Powell Wendy, Grove Joseph, Savage Caroline O S, Wakelam Michael J O
CR-UK Institute for Cancer Studies, Birmingham University, Birmingham B15 2TT, UK.
J Am Soc Nephrol. 2007 Apr;18(4):1112-20. doi: 10.1681/ASN.2006090973. Epub 2007 Mar 14.
Patients with certain forms of systematic vasculitis, such as Wegener's granulomatosis, have circulating antineutrophil cytoplasmic antibodies (ANCA). These inappropriately stimulate circulating neutrophils adhere to and thereby obstruct small vessels. This, together with ANCA-induced degranulation and an oxidative burst, leads to local tissue damage. The signaling pathways that are activated by ANCA IgG are distinct from those that are involved in normal neutrophil activation. This study shows that diacylglycerol kinase is selectively activated by ANCA and that the generated phosphatidic acid is responsible for promoting neutrophil adhesion, in part through integrin activation. The data presented point to diacylglycerol kinase alpha as a novel but selective target for the development of drugs to treat this potentially fatal disorder.
患有某些形式的系统性血管炎(如韦格纳肉芽肿病)的患者体内存在循环抗中性粒细胞胞浆抗体(ANCA)。这些抗体会不恰当地刺激循环中的中性粒细胞黏附,从而阻塞小血管。这与ANCA诱导的脱颗粒和氧化爆发一起,导致局部组织损伤。ANCA IgG激活的信号通路与正常中性粒细胞激活所涉及的信号通路不同。这项研究表明,二酰基甘油激酶被ANCA选择性激活,所产生的磷脂酸部分通过整合素激活,负责促进中性粒细胞黏附。所呈现的数据表明,二酰基甘油激酶α是开发治疗这种潜在致命疾病药物的一个新的但具有选择性的靶点。