Lordier Larissa, Di Buduo Christian A, Kauskot Alexandre, Balayn Nathalie, Lavenu-Bombled Cécile, Baschieri Francesco, Proulle Valérie, Oyarzun Cecilia P Marin, Careddu Francesca, Biunno Ida, Manoliu Tudor, Rameau Philippe, Plo Isabelle, Papadopoulos Nicolas, Constantinescu Stefan, Vainchenker William, Nguyen Guillaume Nam, Ballerini Paola, Favier Remi, Balduini Alessandra, Raslova Hana
INOVARION, Paris, France; INSERM, UMR1287, Gustave Roussy, Villejuif, France, Equipe labellisée Ligue Nationale Contre le Cancer; Université Paris-Saclay, UMR 1287, Gustave Roussy, Villejuif, France; Gustave Roussy, UMR 1287, Villejuif.
Department of Molecular Medicine, University of Pavia, Pavia.
Haematologica. 2025 Jul 1;110(7):1596-1609. doi: 10.3324/haematol.2024.286424. Epub 2025 Mar 6.
Bernard Soulier syndrome (BSS) is a severe bleeding disorder with moderate to severe thrombocytopenia, giant platelets, and platelet dysfunction, caused by biallelic mutations in GP1BA, GP1BB, or GP9 genes. We generated induced pluripotent stem cells (iPSC) from a BSS patient with a novel heterozygous GP1BA p.N103D mutation, resulting in moderate macrothrombocytopenia. The mutation does not affect megakaryocyte (MK) differentiation or GPIb-GPIX complex expression but reduces affinity to von Willebrand factor (VWF). It induces increased signaling independent of VWF and αIIbβ3-mediated outside-in signaling, causing a profound defect in proplatelet formation after adhesion on fibrinogen. Pre-activation of αIIbβ3 integrin and heightened stress fiber formation linked to RhoA pathway overactivation were observed, likely due to increased phosphorylation of SRC at Y419 downstream of GPIbα. Dasatinib, a SRC inhibitor, restored stress fiber formation. Using a 3D bone marrow model to mimic platelet release under flow, we demonstrated that the ROCK1/2 inhibitor Y27632 increased platelet number and restored platelet size in GPIbαN103D MK, as well as in MK from two other patients with heterozygous GP1BA mutations (p.L160P and p.N150S). However, Y27632 had no additional effect on platelet generation from MK of two patients with biallelic BSS, suggesting a distinct molecular mechanism in biallelic cases.
伯纳德-索利尔综合征(BSS)是一种严重的出血性疾病,伴有中度至重度血小板减少、巨大血小板和血小板功能障碍,由GP1BA、GP1BB或GP9基因的双等位基因突变引起。我们从一名患有新型杂合性GP1BA p.N103D突变的BSS患者中生成了诱导多能干细胞(iPSC),该突变导致中度大血小板减少。该突变不影响巨核细胞(MK)分化或糖蛋白Ib-糖蛋白IX(GPIb-GPIX)复合物表达,但降低了与血管性血友病因子(VWF)的亲和力。它诱导了与VWF和αIIbβ3介导的外向内信号无关的信号增加,导致在纤维蛋白原上黏附后前血小板形成出现严重缺陷。观察到αIIbβ3整合素的预激活和与RhoA途径过度激活相关的应激纤维形成增强,这可能是由于GPIbα下游的SRC在Y位点419处磷酸化增加所致。SRC抑制剂达沙替尼恢复了应激纤维形成。使用3D骨髓模型模拟流动状态下的血小板释放,我们证明ROCK1/2抑制剂Y27632增加了GPIbαN103D MK以及另外两名携带杂合性GP1BA突变(p.L160P和p.N150S)患者的MK中的血小板数量,并恢复了血小板大小。然而,Y27632对两名双等位基因BSS患者的MK产生的血小板没有额外影响,这表明双等位基因病例存在独特的分子机制。