Centre de recherche, INSERM U823-CNRS ERL 3148, Université J. Fourier, Grenoble, France.
FEBS J. 2010 Mar;277(5):1084-96. doi: 10.1111/j.1742-4658.2009.07537.x. Epub 2010 Jan 22.
Cerebral cavernous malformations (CCM) are common vascular malformations with an unpredictable risk of hemorrhage, the consequences of which range from headache to stroke or death. Three genes, CCM1, CCM2 and CCM3, have been linked to the disease. The encoded CCM proteins interact with each other within a large protein complex. Within the past 2 years, a plethora of new data has emerged on the signaling pathways in which CCM proteins are involved. CCM proteins regulate diverse aspects of endothelial cell morphogenesis and blood vessel stability such as cell-cell junctions, cell shape and polarity, or cell adhesion to the extracellular matrix. Although fascinating, a global picture is hard to depict because little is known about how these pathways coordinate to orchestrate angiogenesis. Here we present what is known about the structural domain organization of CCM proteins, their association as a ternary complex and their subcellular localization. Numerous CCM partners have been identified using two-hybrid screens, genetic analyses or proteomic studies. We focus on the best-characterized partners and review data on the signaling pathways they regulate as a step towards a better understanding of the etiology of CCM disease.
脑静脉畸形(CCM)是常见的血管畸形,具有不可预测的出血风险,其后果从头痛到中风甚至死亡不等。已有三个基因(CCM1、CCM2 和 CCM3)与该疾病相关。编码的 CCM 蛋白在一个大型蛋白复合物内相互作用。在过去的 2 年中,大量新数据揭示了 CCM 蛋白参与的信号通路。CCM 蛋白调节内皮细胞形态发生和血管稳定性的多个方面,如细胞-细胞连接、细胞形状和极性,或细胞与细胞外基质的黏附。尽管引人入胜,但由于对这些途径如何协调以协调血管生成知之甚少,因此很难描绘出全貌。在这里,我们介绍了 CCM 蛋白的结构域组织、它们作为三元复合物的关联以及它们的亚细胞定位。已经使用双杂交筛选、遗传分析或蛋白质组学研究鉴定了许多 CCM 伴侣。我们重点介绍了研究最充分的伴侣,并回顾了它们调节的信号通路的数据,以期更好地了解 CCM 疾病的病因。