Skowronek Dariush, Pilz Robin A, Saenko Valeriia V, Mellinger Lara, Singer Debora, Ribback Silvia, Weise Anja, Claaßen Kevin, Büttner Christian, Brockmann Emily M, Hübner Christian A, Aung Thiha, Haerteis Silke, Bekeschus Sander, Ekici Arif B, Felbor Ute, Rath Matthias
Department of Human Genetics, University Medicine Greifswald and Interfaculty Institute of Genetics and Functional Genomics, University of Greifswald, Fleischmannstraße 43, 17475, Greifswald, Germany.
Department of Dermatology and Venerology, Rostock University Medical Center, Rostock, Germany.
Angiogenesis. 2025 Jun 6;28(3):32. doi: 10.1007/s10456-025-09985-5.
Cerebral cavernous malformations (CCMs) are clusters of thin-walled enlarged blood vessels in the central nervous system that are prone to recurrent hemorrhage and can occur in both sporadic and familial forms. The familial form results from loss-of-function variants in the CCM1, CCM2, or CCM3 gene. Despite a better understanding of CCM pathogenesis in recent years, it is still unclear why CCM3 mutations often lead to a more aggressive phenotype than CCM1 or CCM2 variants. By combining high-throughput differentiation of blood vessel organoids from human induced pluripotent stem cells (hiPSCs) with a CCM1, CCM2, or CCM3 knockout, single-cell RNA sequencing, and high-content imaging, we uncovered both shared and distinct functions of the CCM proteins. While there was a significant overlap of differentially expressed genes in fibroblasts across all three knockout conditions, inactivation of CCM1, CCM2, or CCM3 also led to specific gene expression patterns in neuronal, mesenchymal, and endothelial cell populations, respectively. Taking advantage of the different fluorescent labels of the hiPSCs, we could also visualize the abnormal expansion of CCM1 and CCM3 knockout cells when differentiated together with wild-type cells into mosaic blood vessel organoids. In contrast, CCM2 knockout cells showed even reduced proliferation. These observations may help to explain the less severe clinical course in individuals with a pathogenic variant in CCM2 and to decode the molecular and cellular heterogeneity in CCM disease. Finally, the excellent scalability of blood vessel organoid differentiation in a 96-well format further supports their use in high-throughput drug discovery and other biomedical research studies.
脑海绵状血管畸形(CCMs)是中枢神经系统中薄壁扩张血管的簇集,容易反复出血,可呈散发性和家族性形式出现。家族性形式是由CCM1、CCM2或CCM3基因的功能丧失变异引起的。尽管近年来对CCM发病机制有了更好的理解,但仍不清楚为什么CCM3突变通常比CCM1或CCM2变异导致更具侵袭性的表型。通过将人诱导多能干细胞(hiPSCs)的血管类器官高通量分化与CCM1、CCM2或CCM3基因敲除、单细胞RNA测序和高内涵成像相结合,我们揭示了CCM蛋白的共同和独特功能。虽然在所有三种基因敲除条件下成纤维细胞中差异表达基因有显著重叠,但CCM1、CCM2或CCM3的失活也分别导致神经元、间充质和内皮细胞群体中的特定基因表达模式。利用hiPSCs的不同荧光标记,当与野生型细胞一起分化为嵌合血管类器官时,我们还可以观察到CCM1和CCM3基因敲除细胞的异常扩张。相比之下,CCM2基因敲除细胞的增殖甚至减少。这些观察结果可能有助于解释CCM2致病变异个体临床病程较轻的原因,并解码CCM疾病中的分子和细胞异质性。最后,96孔板格式的血管类器官分化具有出色的可扩展性,进一步支持了它们在高通量药物发现和其他生物医学研究中的应用。