INSERM U770, Le Kremlin-Bicêtre, F-94276, France ; Univ Paris-Sud, UMR_S770, Le Kremlin-Bicêtre, F-94276, France.
Mediterr J Hematol Infect Dis. 2013 Jul 10;5(1):e2013047. doi: 10.4084/MJHID.2013.047. Print 2013.
Up until recently, von Willebrand Factor (VWF) structure-function relationships have only been studied through in vitro approaches. A powerful technique known as hydrodynamic gene transfer, which allows transient expression of a transgene by mouse hepatocytes, has led to an important shift in VWF research. Indeed this approach has now enabled us to transiently express a number of VWF mutants in VWF-deficient mice in order to test the relative importance of specific residues in different aspects of VWF biology and functions in an in vivo setting. As a result, mice reproducing various types of von Willebrand disease have been generated, models that will be useful to test new therapies. This approach also allowed a more precise identification of the importance of VWF interaction with subendothelial collagens and with platelets receptors in hemostasis and thrombosis. The recent advances gathered from these studies as well as the pros and cons of the technique will be reviewed here.
直到最近,人们还只是通过体外方法研究 von Willebrand 因子(VWF)的结构-功能关系。一种称为流体动力学基因转移的强大技术,可使小鼠肝细胞瞬时表达转基因,这一技术引发了 VWF 研究的重要转变。事实上,这种方法现在使我们能够在 VWF 缺陷型小鼠中瞬时表达多种 VWF 突变体,以在体内环境中测试特定残基在 VWF 生物学和功能的不同方面的相对重要性。结果,产生了复制各种类型 von Willebrand 病的小鼠,这些模型将有助于测试新的治疗方法。这种方法还可以更准确地确定 VWF 与内皮下胶原和血小板受体相互作用在止血和血栓形成中的重要性。本文将回顾这些研究中汇集的最新进展以及该技术的优缺点。