Hato T, Pampori N, Shattil S J
Department of Vascular Biology, The Scripps Research Institute, La Jolla, California, USA.
J Cell Biol. 1998 Jun 29;141(7):1685-95. doi: 10.1083/jcb.141.7.1685.
Integrin alphaIIb beta3 mediates platelet aggregation and "outside-in" signaling. It is regulated by changes in receptor conformation and affinity and/or by lateral diffusion and receptor clustering. To document the relative contributions of conformation and clustering to alphaIIb beta3 function, alphaIIb was fused at its cytoplasmic tail to one or two FKBP12 repeats (FKBP). These modified alphaIIb subunits were expressed with beta3 in CHO cells, and the heterodimers could be clustered into morphologically detectable oligomers upon addition of AP1510, a membrane-permeable, bivalent FKBP ligand. Integrin clustering by AP1510 caused binding of fibrinogen and a multivalent (but not monovalent) fibrinogen-mimetic antibody. However, ligand binding due to clustering was only 25-50% of that observed when alphaIIb beta3 affinity was increased by an activating antibody or an activating mutation. The effects of integrin clustering and affinity modulation were additive, and clustering promoted irreversible ligand binding. Clustering of alphaIIb beta3 also promoted cell adhesion to fibrinogen or von Willebrand factor, but not as effectively as affinity modulation. However, clustering was sufficient to trigger fibrinogen-independent tyrosine phosphorylation of pp72(Syk) and fibrinogen-dependent phosphorylation of pp125(FAK), even in non-adherent cells. Thus, receptor clustering and affinity modulation play complementary roles in alphaIIb beta3 function. Affinity modulation is the predominant regulator of ligand binding and cell adhesion, but clustering increases these responses further and triggers protein tyrosine phosphorylation, even in the absence of affinity modulation. Both affinity modulation and clustering may be needed for optimal function of alphaIIb beta3 in platelets.
整合素αIIbβ3介导血小板聚集和“由外向内”信号传导。它受受体构象和亲和力的变化和/或侧向扩散及受体聚集的调节。为了证明构象和聚集对αIIbβ3功能的相对贡献,将αIIb在其胞质尾部与一或两个FKBP12重复序列(FKBP)融合。这些修饰的αIIb亚基与β3在CHO细胞中共同表达,加入AP1510(一种可透过膜的二价FKBP配体)后,异二聚体可聚集成形态上可检测到的寡聚体。AP1510介导的整合素聚集导致纤维蛋白原和一种多价(而非单价)纤维蛋白原模拟抗体的结合。然而,由聚集引起的配体结合仅为通过激活抗体或激活突变增加αIIbβ3亲和力时所观察到的结合的25 - 50%。整合素聚集和亲和力调节的作用是相加的,且聚集促进不可逆的配体结合。αIIbβ3的聚集也促进细胞与纤维蛋白原或血管性血友病因子的黏附,但不如亲和力调节有效。然而,即使在非黏附细胞中,聚集也足以触发pp72(Syk)的非纤维蛋白原依赖性酪氨酸磷酸化和pp125(FAK)的纤维蛋白原依赖性磷酸化。因此,受体聚集和亲和力调节在αIIbβ3功能中发挥互补作用。亲和力调节是配体结合和细胞黏附的主要调节因子,但聚集进一步增强这些反应,并触发蛋白质酪氨酸磷酸化,即使在没有亲和力调节的情况下也是如此。血小板中αIIbβ3的最佳功能可能需要亲和力调节和聚集两者。