Department of Biological Sciences, University of North Texas, Denton, TX 76203, USA.
Blood Cells Mol Dis. 2010 Dec 15;45(4):326-33. doi: 10.1016/j.bcmd.2010.10.002. Epub 2010 Oct 29.
von Willebrand factor (vWF) is a large protein involved in primary hemostasis. A dysfunction in this protein or an insufficient production of the protein leads to improper platelet adhesion/aggregation, resulting in a bleeding phenotype known as von Willebrand disease (vWD). To gain a better understanding of vWF interactions in vivo, the use of zebrafish as a model is ideal because of the transparency of the embryos and larvae. In this article, we examined the presence and function of vWF in hemostasis of zebrafish utilizing a variety of molecular methods. Using RT-PCR and antibody staining, we have shown that vWF mRNA is present in thrombocytes. Through antibody staining, we demonstrated vWF is synthesized in blood vessels. The role of zebrafish vWF in hemostasis was established through knockdown methods using vWF morpholino (vWF MO) antisense oligonucleotides. Embryos injected with vWF MO at the one to four cell stages resulted in a bleeding phenotype. Injection of embryos with vWF MO also caused an increase in time to occlusion within arteries in larvae upon laser induced injury. We then used vWF-specific Vivo-morpholinos (VMO) to induce vWF knockdown in adult zebrafish by targeting the exon homologous to the human exon 28 of the vWF gene. The reduced ristocetin-mediated agglutination of thrombocytes in a plate tilting assay, using blood from adult zebrafish injected with VMO, provided evidence that vWF is involved in the hemostatic process. We also administered desmopressin acetate to larvae and adults which resulted in enhanced aggregation/agglutination of thrombocytes. Zebrafish genome database analysis revealed the presence of GPIbβ gene. It also revealed the exon of zebrafish vWF gene corresponding to exon 28 of human vWF gene is highly similar to the exon 28 of human vWF gene, except that it has an insertion that leads to a translated peptide sequence that separates the two A domains coded by this exon. This exon is also conserved in other fishes. In summary, we established that zebrafish vWF has a role similar to that of vWF found in humans, thus, making zebrafish a useful model for studying the cell biology of vWF in vivo.
血管性血友病因子(vWF)是一种参与初级止血的大型蛋白。该蛋白功能障碍或其蛋白产生不足会导致血小板黏附/聚集不当,导致一种称为血管性血友病(vWD)的出血表型。为了更好地了解 vWF 在体内的相互作用,使用斑马鱼作为模型是理想的,因为斑马鱼胚胎和幼鱼具有透明性。在本文中,我们利用各种分子方法检查了 vWF 在斑马鱼止血中的存在和功能。通过 RT-PCR 和抗体染色,我们已经证明 vWF mRNA 存在于血小板中。通过抗体染色,我们证明 vWF 在血管中合成。通过使用 vWF 形态发生素(vWF MO)反义寡核苷酸进行基因敲低方法,确立了斑马鱼 vWF 在止血中的作用。在一至四个细胞阶段注射 vWF MO 的胚胎导致出血表型。注射 vWF MO 的胚胎也导致在激光诱导损伤后幼鱼的动脉闭塞时间增加。然后,我们使用针对与 vWF 基因人外显子 28 同源的外显子的 vWF 特异性 Vivo-morpholinos(VMO),通过靶向成年斑马鱼中的 vWF 基因,在成年斑马鱼中诱导 vWF 基因敲低。在使用来自注射 VMO 的成年斑马鱼的血液进行的平板倾斜测定中,血小板的瑞斯托菌素介导的聚集减少提供了 vWF 参与止血过程的证据。我们还向幼虫和成年斑马鱼施用醋酸去氨加压素,导致血小板聚集/聚集增强。斑马鱼基因组数据库分析显示存在 GPIbβ 基因。它还揭示了斑马鱼 vWF 基因的外显子与人类 vWF 基因的外显子 28 高度相似,除了它有一个插入导致翻译的肽序列,将该外显子编码的两个 A 结构域分开。这个外显子在其他鱼类中也被保守。总之,我们确立了斑马鱼 vWF 具有与人类 vWF 相似的作用,因此,使斑马鱼成为研究体内 vWF 细胞生物学的有用模型。