Hubrecht Institute-KNAW and UMC, Utrecht, the Netherlands.
J Thromb Haemost. 2010 Mar;8(3):588-95. doi: 10.1111/j.1538-7836.2009.03721.x. Epub 2009 Dec 11.
We have used the advantages of the zebrafish model system to demonstrate which of the vertebrate myosin light chain kinase (MLCK) genes is expressed in thrombocytes and important for thrombus formation.
Here we report that Mlck1a is an essential component of thrombus formation. Phylogenetic data revealed four zebrafish orthologous for three human MLCK genes. To investigate expression of the zebrafish mlck genes in thrombocytes we compared GFP-tagged platelets with other cells by microarray analysis, and showed that mlck1a expression was 4.5-fold enriched in platelets. Furthermore, mlck1a mRNA and mRNA for the platelet-specific cd41 co-localized in thrombi. Expression of other mlck subtypes was lower in GFP-tagged platelets (mlck1b; 0.77-fold enriched) and absent in thrombi (mlck1b, -2, -3). To investigate the role of Mlck1a in thrombus formation, we knocked down mlck1a using two morpholinos. This resulted in impaired morphology changes of platelets adhering on fibrinogen. In a thrombosis model, in which thrombocytes adhere to the vessel wall damaged by laser irradiation, thrombus formation was slowed down in mlck1a-deficient embryos.
We conclude that Mlck1a is the subtype of MLCK that contributes to platelet shape change and thrombus formation.
我们利用斑马鱼模型系统的优势,证明了脊椎动物肌球蛋白轻链激酶(MLCK)基因中的哪一种在血小板中表达,并对血栓形成很重要。
在这里,我们报告 Mlck1a 是血栓形成的一个重要组成部分。系统发育数据分析揭示了四个与人类三个 MLCK 基因同源的斑马鱼基因。为了研究斑马鱼 mlck 基因在血小板中的表达,我们通过微阵列分析比较了 GFP 标记的血小板与其他细胞,结果表明 mlck1a 在血小板中的表达富集了 4.5 倍。此外,mlck1a mRNA 和血小板特异性 cd41 的 mRNA 在血栓中共同定位。其他 mlck 亚型在 GFP 标记的血小板中的表达水平较低(mlck1b 富集了 0.77 倍),在血栓中不存在(mlck1b、-2、-3)。为了研究 Mlck1a 在血栓形成中的作用,我们使用两种莫洛尼氏干扰 RNA 敲低了 mlck1a。这导致血小板在纤维蛋白原上黏附时形态变化受损。在血栓形成模型中,当血小板黏附在激光照射损伤的血管壁上时,mlck1a 缺陷型胚胎中的血栓形成速度减慢。
我们得出结论,Mlck1a 是参与血小板形态变化和血栓形成的 MLCK 亚型。