Italiano Joseph E, Bergmeier Wolfgang, Tiwari Sanjay, Falet Hervé, Hartwig John H, Hoffmeister Karin M, André Patrick, Wagner Denisa D, Shivdasani Ramesh A
Division of Hematology and Department of Medicine, Brigham & Women's Hospital and Harvard Medical School, Boston, MA, USA.
Blood. 2003 Jun 15;101(12):4789-96. doi: 10.1182/blood-2002-11-3491. Epub 2003 Feb 13.
The platelet marginal band consists of a single peripheral microtubule (MT) that is wound in 8 to 12 coils and maintains discoid cell shape. About 90% of beta-tubulin in the marginal band is of the divergent, megakaryocyte (MK)/platelet-restricted beta1 isoform. beta1-tubulin-null mice show reduced proplatelet formation, thrombocytopenia, and platelet spherocytosis. Here, we show that structural abnormalities in resting beta1-tubulin-/- platelets include frequent kinks and breaks in the marginal band. Platelets derived from mice lacking the transcription factor GATA1 show similar defects, probably as a direct consequence of absent beta1-tubulin. beta1-tubulin+/- platelets have normal ratios of beta-tubulin isotypes but the marginal band is half the normal thickness, which is sufficient to maintain elliptical cell shape. Thus, a threshold 50% or less of the normal amount of beta1-tubulin is required to preserve marginal band integrity and cell shape. beta1-tubulin-/- platelets have normal size and contents and show no defects in serotonin release or aggregation. Accordingly, the apparently isolated spherocytosis allows investigation of the role of discoid platelet shape in hemostasis. On agonist stimulation, the disorganized MTs in beta1-tubulin-/- platelets fail to condense into central rings and instead are dispersed in short bundles and linear arrays. Nevertheless, intravital microscopy and flow chamber studies demonstrate full functionality of these spherocytic platelets under physiologic shear conditions. Together, these findings highlight the essential requirements of the MK/platelet-restricted beta1-tubulin isoform in platelet structure and suggest that spherocytosis does not impair many aspects of platelet function.
血小板边缘带由一条外周微管组成,该微管呈8至12个盘绕,维持盘状细胞形态。边缘带中约90%的β-微管蛋白是分化型、巨核细胞(MK)/血小板特异性的β1亚型。β1-微管蛋白基因敲除小鼠的前血小板形成减少、血小板减少和血小板球形化。在此,我们发现静息状态下β1-微管蛋白基因敲除血小板的结构异常包括边缘带频繁出现扭结和断裂。缺乏转录因子GATA1的小鼠来源的血小板也有类似缺陷,可能是β1-微管蛋白缺失的直接后果。β1-微管蛋白杂合子血小板的β-微管蛋白同工型比例正常,但边缘带厚度只有正常的一半,这足以维持椭圆形细胞形态。因此,维持边缘带完整性和细胞形态所需的β1-微管蛋白阈值为正常量的50%或更低。β1-微管蛋白基因敲除血小板大小和内容物正常,在5-羟色胺释放或聚集方面无缺陷。因此,明显孤立的球形化现象有助于研究盘状血小板形态在止血中的作用。在激动剂刺激下,β1-微管蛋白基因敲除血小板中紊乱的微管无法浓缩成中央环,而是分散成短束和线性阵列。然而,活体显微镜和流动腔室研究表明,这些球形血小板在生理剪切条件下具有完全功能。总之,这些发现突出了MK/血小板特异性β1-微管蛋白同工型在血小板结构中的基本需求,并表明球形化并不损害血小板功能的许多方面。