Pasquier Benoit, Launay Pierre, Kanamaru Yutaka, Moura Ivan C, Pfirsch Séverine, Ruffié Claude, Hénin Dominique, Benhamou Marc, Pretolani Marina, Blank Ulrich, Monteiro Renato C
INSERM U699, Bichat Medical School, 16 rue Henri Huchard, 75870 Paris Cedex 18, France.
Immunity. 2005 Jan;22(1):31-42. doi: 10.1016/j.immuni.2004.11.017.
Serum IgA is considered a discrete housekeeper of the immune system with multiple anti-inflammatory functions, whereas IgA-immune complexes mediate inflammatory responses. Here, we identify FcalphaRI as a molecular device that determines the nature of IgA responses. In the absence of sustained aggregation, receptor targeting by serum IgA or anti-FcalphaRI Fab inhibits activating responses of heterologous FcgammaR or FcepsilonRI. The inhibitory mechanism involves recruitment of tyrosine phosphatase SHP-1 to FcalphaRI and impairment of Syk, LAT, and ERK phosphorylation induced by FcepsilonRI engagement. SHP-1 recruitment is dependent on ERK. Conversely, sustained aggregation of FcalphaRI by multimeric ligands stimulates cell activation by recruiting high amounts of Syk and aborting SHP-1 binding. Both types of signals require the FcRgamma-ITAM motif. Anti-FcalphaRI Fab treatment suppresses manifestations of allergic asthma in FcalphaRI transgenic mice. These findings redefine FcalphaRI as a bifunctional inhibitory/activating receptor of the immune system that mediates both anti- and proinflammatory functions of IgA.
血清IgA被认为是具有多种抗炎功能的免疫系统离散管家,而IgA免疫复合物介导炎症反应。在此,我们确定FcalphaRI是一种决定IgA反应性质的分子装置。在没有持续聚集的情况下,血清IgA或抗FcalphaRI Fab对受体的靶向作用会抑制异源FcgammaR或FcepsilonRI的激活反应。抑制机制涉及酪氨酸磷酸酶SHP-1募集到FcalphaRI以及FcepsilonRI结合诱导的Syk、LAT和ERK磷酸化受损。SHP-1募集依赖于ERK。相反,多聚配体使FcalphaRI持续聚集通过募集大量Syk并阻止SHP-1结合来刺激细胞活化。两种类型的信号都需要FcRgamma-ITAM基序。抗FcalphaRI Fab治疗可抑制FcalphaRI转基因小鼠过敏性哮喘的表现。这些发现将FcalphaRI重新定义为免疫系统的双功能抑制/激活受体,其介导IgA的抗炎和促炎功能。