MTA-ELTE 'Lendület' Complement Research Group, Department of Immunology, Eötvös Loránd University, Budapest, Hungary.
Centro de Investigaciones Biológicas, Consejo Superior de Investigaciones Científicas, Madrid, Spain; Centro de Investigación Biomédica en Enfermedades Raras, Madrid, Spain.
Trends Immunol. 2015 Jun;36(6):374-84. doi: 10.1016/j.it.2015.04.008. Epub 2015 May 13.
Complement factor H-related proteins (FHRs) are strongly associated with different diseases involving complement dysregulation, which suggests a major role for these proteins regulating complement activation. Because FHRs are evolutionarily and structurally related to complement inhibitor factor H (FH), the initial assumption was that the FHRs are also negative complement regulators. Whereas weak complement inhibiting activities were originally reported for these molecules, recent developments indicate that FHRs may enhance complement activation, with important implications for the role of these proteins in health and disease. We review these findings here, and propose that FHRs represent a complex set of surface recognition molecules that, by competing with FH, provide improved discrimination of self and non-self surfaces and play a central role in determining appropriate activation of the complement pathway.
补体因子 H 相关蛋白(FHRs)与涉及补体失调的多种疾病密切相关,这表明这些蛋白在调节补体激活方面发挥着重要作用。由于 FHRs 在进化和结构上与补体抑制剂因子 H(FH)相关,最初的假设是 FHRs 也是负性补体调节剂。尽管最初报道这些分子具有较弱的补体抑制活性,但最近的研究进展表明 FHRs 可能增强补体激活,这对这些蛋白在健康和疾病中的作用具有重要意义。我们在此综述了这些发现,并提出 FHRs 代表了一组复杂的表面识别分子,通过与 FH 竞争,提供了对自身和非自身表面的更好区分,并在确定补体途径的适当激活方面发挥着核心作用。