Ramirez Francesco, Dietz Harry C
Child Health Institute of New Jersey, Robert W. Johnson Medical School, New Brunswick, New York 08901, USA.
J Cell Physiol. 2007 Nov;213(2):326-30. doi: 10.1002/jcp.21189.
Fibrillin-rich microfibrils are specialized extracellular matrix assemblies that endow connective tissues with mechanical stability and elastic properties, and that participate in the regulation of organ formation, growth and homeostasis. Their physiological importance is underscored by the complex spectrum of clinical manifestations associated with mutations of fibrillin-1 and fibrillin-2 in Marfan syndrome (MFS) and congenital contractural arachnodactyly, respectively. Early evidence suggested that fibrillin-1 mutations in MFS lead to loss of tissue integrity by perturbing microfibril assembly and function. Recent studies in genetically targeted mice have however revealed that fibrillin-1 and fibrillin-2 mutations perturb signaling events mediated by TGF-beta superfamily members. As such, these studies have established a new biological paradigm whereby fibrillin-rich microfibrils are structural networks that specify the local concentration and timely release of signaling molecules during morphogenesis and tissue remodeling. This review summarizes our current understanding of the role of fibrillin-rich microfibrils in development and disease, as well as exciting new applications in the clinical management of MFS and related connective tissue disorders.
富含原纤蛋白的微原纤维是特殊的细胞外基质组件,赋予结缔组织机械稳定性和弹性特性,并参与器官形成、生长和体内平衡的调节。原纤蛋白-1和原纤蛋白-2的突变分别与马凡综合征(MFS)和先天性挛缩性蜘蛛指症相关的复杂临床表现谱,突出了它们的生理重要性。早期证据表明,MFS中原纤蛋白-1的突变通过扰乱微原纤维的组装和功能导致组织完整性丧失。然而,最近对基因靶向小鼠的研究表明,原纤蛋白-1和原纤蛋白-2的突变扰乱了由转化生长因子-β超家族成员介导的信号事件。因此,这些研究建立了一种新的生物学范式,即富含原纤蛋白的微原纤维是在形态发生和组织重塑过程中指定信号分子局部浓度和及时释放的结构网络。本综述总结了我们目前对富含原纤蛋白的微原纤维在发育和疾病中的作用的理解,以及在MFS和相关结缔组织疾病临床管理中的令人兴奋的新应用。