*Faculty of Medicine, Department of Anatomy and Cell Biology, McGill University, Montreal, QC, Canada, H3A 0C7.
Biochem J. 2013 Dec 1;456(2):283-95. doi: 10.1042/BJ20130699.
Fibrillins constitute the backbone of extracellular multifunctional assemblies present in elastic and non-elastic matrices, termed microfibrils. Assembly of fibrillins into microfibrils and their homoeostasis is poorly understood and is often compromised in connective tissue disorders such as Marfan syndrome and other fibrillinopathies. Using interaction mapping studies, we demonstrate that fibrillins require the complete gelatin-binding region of fibronectin for interaction, which comprises domains FNI6-FNI9. However, the interaction of fibrillin-1 with the gelatin-binding domain of fibronectin is not involved in fibrillin-1 network assembly mediated by human skin fibroblasts. We show further that the fibronectin network is essential for microfibril homoeostasis in early stages. Fibronectin is present in extracted mature microfibrils from tissue and cells as well as in some in situ microfibrils observed at the ultrastructural level, indicating an extended mechanism for the involvement of fibronectin in microfibril assembly and maturation.
原纤维蛋白构成了细胞外多功能组装体的骨架,存在于弹性和非弹性基质中,称为微纤维。微纤维中原纤维蛋白的组装及其同型平衡理解甚少,在马凡综合征和其他原纤维蛋白病等结缔组织疾病中经常受到损害。通过相互作用图谱研究,我们证明原纤维蛋白需要纤维连接蛋白的完整明胶结合区域才能相互作用,该区域包含 FNI6-FNI9 结构域。然而,原纤维蛋白-1 与纤维连接蛋白明胶结合结构域的相互作用并不参与人皮肤成纤维细胞介导的原纤维蛋白-1 网络组装。我们进一步表明,在早期阶段,纤维连接蛋白网络对于微纤维的同型平衡是必需的。纤维连接蛋白存在于组织和细胞中提取的成熟微纤维中,以及在超微结构水平观察到的一些原位微纤维中,这表明纤维连接蛋白参与微纤维组装和成熟的机制是扩展的。