Nataf S, Stahel P F, Davoust N, Barnum S R
Dept of Microbiology, University of Alabama at Birmingham, Birmingham, AL 35294-0005, USA.
Trends Neurosci. 1999 Sep;22(9):397-402. doi: 10.1016/s0166-2236(98)01390-3.
Activation of the complement system has been reported in a variety of inflammatory diseases and neurodegenerative processes of the CNS. Recent evidence indicates that complement proteins and receptors are synthesized on or by glial cells and, surprisingly, neurons. Among these proteins are the receptors for the chemotactic and anaphylactic peptides, C5a and C3a, which are the most-potent mediators of complement inflammatory functions. The functions of glial-cell C3a and C5a receptors (C3aR and C5aR) appear to be similar to immune-cell C3aRs and C5aRs. However, little is known about the roles these receptors might have on neurons. Indeed, when compared with glial cells, neurons display a distinct pattern of C3aR and C5aR expression, in either the normal or the inflamed CNS. These findings suggest unique functions for these receptors on neurons.
在多种炎症性疾病和中枢神经系统的神经退行性过程中,均有补体系统激活的报道。最近的证据表明,补体蛋白和受体是由神经胶质细胞合成的,令人惊讶的是,神经元也能合成。这些蛋白中包括趋化肽和过敏肽C5a和C3a的受体,它们是补体炎症功能最有效的介质。神经胶质细胞C3a和C5a受体(C3aR和C5aR)的功能似乎与免疫细胞C3aR和C5aR相似。然而,对于这些受体在神经元上可能发挥的作用却知之甚少。事实上,与神经胶质细胞相比,在正常或炎症状态的中枢神经系统中,神经元均呈现出独特的C3aR和C5aR表达模式。这些发现提示了这些受体在神经元上具有独特功能。