Wu Shu-Yan, Wang Zhao-Yue, Dai Lan, Huang Rui, Wang Xiang-Ying, Li Su-An, Mao Di-Hua, Ruan Chang-Geng
Jiangsu Institute of Hematology, The First Affiliated Hospital of Suzhou University, Suzhou 215006, China.
Zhonghua Xue Ye Xue Za Zhi. 2006 Sep;27(9):584-7.
To study the platelet morphology and function of an inherited macrothrombocytopenia disorder with abnormal large granules.
Platelet size and structure were investigated by both light microscopy and electron microscopy. The platelet membrane expression of GP I b, GP II b, GPIII a, P-selectin and CD63 were analyzed by using respective monoclonal antibodies. Platelet 5-hydroxy-tryptamine was measured with spectrophotofluorometer.
Both the patient and her father had large granules in their platelets, with exocytosis being easily observed. The expressions of GP I b, GP II b and GP II a on the platelets were in normal range, while P-selectin and CD63 were somewhat increased. The abnormal large granules were not the alpha granules, lysosomes or dense bodies.
Both morphological and functional abnormalities of the platelets from the patient are clearly distinguishable from other hereditary giant platelet disorders. It would probably represent a novel platelet disorder.
研究一种伴有异常大颗粒的遗传性巨血小板减少症的血小板形态和功能。
通过光学显微镜和电子显微镜研究血小板大小和结构。使用各自的单克隆抗体分析血小板膜上糖蛋白I b、糖蛋白II b、糖蛋白III a、P-选择素和CD63的表达。用分光荧光计测量血小板5-羟色胺。
患者及其父亲的血小板均有大颗粒,且易观察到胞吐作用。血小板上糖蛋白I b、糖蛋白II b和糖蛋白II a的表达在正常范围内,而P-选择素和CD63有所增加。异常大颗粒不是α颗粒、溶酶体或致密体。
患者血小板的形态和功能异常与其他遗传性巨血小板疾病明显不同。它可能代表一种新型血小板疾病。