Molina Hector
Division of Rheumatology, Department of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA.
Immunol Res. 2005;32(1-3):187-92. doi: 10.1385/IR:32:1-3:187.
Complement has an important role in innate immunity and inflammation. Complement also has the capacity to attack self tissues. Cells are protected from the deleterious effects of complement. The Crry protein belongs to a family of molecules that regulates complement activation, protecting tissues from complement-mediated damage. To investigate the role of these molecules in vivo, Crry-/- mice were generated. Crry-/- mice did not survive pregnancy owing to abnormal complement deposition in the placenta through the alternative pathway. Tissue damage related to C5 (production of C5a and C5b-9) was not required. Removal of inflammatory cells did not affect the phenotype. This suggests new noninflammatory mechanisms of pregnancy failure that are dependent solely on C3. The major abnormality was a failure of blood vessel formation in the placenta, revealing an unsuspected C3 effect in the vascular development of this organ.
补体在固有免疫和炎症中发挥着重要作用。补体也具有攻击自身组织的能力。细胞受到保护,免受补体的有害影响。Crry蛋白属于调节补体激活的分子家族,可保护组织免受补体介导的损伤。为了研究这些分子在体内的作用,构建了Crry基因敲除小鼠。Crry基因敲除小鼠由于通过替代途径在胎盘中异常沉积补体而无法存活至妊娠结束。与C5(C5a和C5b-9的产生)相关的组织损伤并非必需。清除炎症细胞并不影响该表型。这提示了仅依赖C3的妊娠失败的新的非炎症机制。主要异常是胎盘血管形成失败,揭示了该器官血管发育中未被怀疑的C3效应。