Mina-Osorio Paola, Ortega Enrique
Department of Immunology, Instituto de Investigaciones Biomédicas. Universidad Nacional Autónoma de México. A.P. 70228 Ciudad Universitaria, DF CP, México.
Trends Immunol. 2004 Oct;25(10):529-35. doi: 10.1016/j.it.2004.08.008.
Leukocyte membrane receptors for the Fc portion of Igs (FcRs) link antigen recognition by antibodies to effector functions involved in immune phenomena, from pathogen elimination to autoimmunity. Moreover, they also signal for the synthesis and secretion of cytokines and chemokines, thus having a role in immune homeostasis. Even though the structural and functional similarities between FcRs and the clonotypic antigen receptors of lymphocytes (the T-cell receptor and B-cell receptor) are well established, participation of regulatory membrane molecules in leukocyte activation by FcRs has rarely been considered. Here, we summarize evidence demonstrating that FcR-mediated signaling could be modulated by other membrane molecules (signal regulators), and propose that comprehension of this phenomenon is essential for understanding the functions of FcRs, knowledge of which could then be used for therapeutic interventions.
免疫球蛋白(Ig)Fc段的白细胞膜受体(FcRs)将抗体介导的抗原识别与免疫现象中的效应功能联系起来,这些效应功能涵盖从病原体清除到自身免疫等多个方面。此外,它们还能为细胞因子和趋化因子的合成与分泌发出信号,从而在免疫稳态中发挥作用。尽管FcRs与淋巴细胞的克隆型抗原受体(T细胞受体和B细胞受体)之间的结构和功能相似性已得到充分证实,但FcRs激活白细胞过程中调节性膜分子的参与却很少被考虑。在此,我们总结了相关证据,证明FcR介导的信号传导可被其他膜分子(信号调节因子)调节,并提出理解这一现象对于理解FcRs的功能至关重要,而对FcRs功能的了解可用于治疗干预。