Department of Molecular Genetics, Biochemistry, and Microbiology, University of Cincinnati, Cincinnati, OH, USA.
Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
Endocrinology. 2023 Jan 9;164(3). doi: 10.1210/endocr/bqad017.
Inhibins are transforming growth factor-β family heterodimers that suppress follicle-stimulating hormone (FSH) secretion by antagonizing activin class ligands. Inhibins share a common β chain with activin ligands. Follistatin is another activin antagonist, known to bind the common β chain of both activins and inhibins. In this study, we characterized the antagonist-antagonist complex of inhibin A and follistatin to determine if their interaction impacted activin A antagonism. We isolated the inhibin A:follistatin 288 complex, showing that it forms in a 1:1 stoichiometric ratio, different from previously reported homodimeric ligand:follistatin complexes, which bind in a 1:2 ratio. Small angle X-ray scattering coupled with modeling provided a low-resolution structure of inhibin A in complex with follistatin 288. Inhibin binds follistatin via the shared activin β chain, leaving the α chain free and flexible. The inhibin A:follistatin 288 complex was also shown to bind heparin with lower affinity than follistatin 288 alone or in complex with activin A. Characterizing the inhibin A:follistatin 288 complex in an activin-responsive luciferase assay and by surface plasmon resonance indicated that the inhibitor complex readily dissociated upon binding type II receptor activin receptor type IIb, allowing both antagonists to inhibit activin signaling. Additionally, injection of the complex in ovariectomized female mice did not alter inhibin A suppression of FSH. Taken together, this study shows that while follistatin binds to inhibin A with a substochiometric ratio relative to the activin homodimer, the complex can dissociate readily, allowing both proteins to effectively antagonize activin signaling.
抑制素是转化生长因子-β家族的异二聚体,通过拮抗激活素类配体抑制卵泡刺激素 (FSH) 的分泌。抑制素与激活素配体共享一个共同的β链。卵泡抑素是另一种激活素拮抗剂,已知它结合激活素和抑制素的共同β链。在这项研究中,我们对抑制素 A 和卵泡抑素的拮抗剂-拮抗剂复合物进行了表征,以确定它们的相互作用是否影响激活素 A 的拮抗作用。我们分离出抑制素 A:卵泡抑素 288 复合物,表明它以 1:1 的化学计量比形成,与之前报道的同源二聚体配体:卵泡抑素复合物不同,后者以 1:2 的比例结合。小角度 X 射线散射与建模相结合,提供了抑制素 A 与卵泡抑素 288 复合物的低分辨率结构。抑制素通过共享的激活素β链与卵泡抑素结合,使α链保持自由和灵活。抑制素 A:卵泡抑素 288 复合物也显示出与肝素的结合亲和力低于卵泡抑素 288 单独或与激活素 A 复合物。在激活素反应性荧光素酶测定和表面等离子体共振中对抑制素 A:卵泡抑素 288 复合物进行表征表明,抑制剂复合物在结合 II 型受体激活素受体 IIb 时很容易解离,从而使两种拮抗剂都能抑制激活素信号。此外,在去卵巢雌性小鼠中注射该复合物不会改变抑制素 A 对 FSH 的抑制作用。总之,这项研究表明,尽管卵泡抑素与激活素同源二聚体相比,与抑制素 A 的结合呈亚化学计量比,但该复合物很容易解离,从而使两种蛋白都能有效地拮抗激活素信号。