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伯纳德-索利尔综合征和赫尔曼斯基-普德拉克综合征中,米帕林标记的致密体数量、血小板积累14C-5-羟色胺的能力与血小板密度之间的关系。

Relationship between mepacrine-labelled dense body number, platelet capacity to accumulate 14C-5-HT and platelet density in the Bernard-Soulier and Hermansky-Pudlak syndromes.

作者信息

Rendu F, Nurden A T, Lebret M, Caen J P

出版信息

Thromb Haemost. 1979 Aug 31;42(2):694-704.

PMID:505374
Abstract

We have used the mepacrine-labelling procedure to measure the dense body (serotonin storage organelle) content of the platelets of 2 hereditary disorders where abnormalities in dense body number were suspected. The platelets were incubated with mepacrine and examined by fluorescence microscopy. A mean number of 5.4 +/- 0.8 (SD) dense bodies per platelet was calculated from the data obtained using platelets isolated from 40 normal human subjects. In contrast the platelets of 2 patients with the Bernard-Soulier syndrome contained an average of 14 and 17 labelled granules. This increase was associated with a much greater capacity of the platelets to accumulate 14C-5-HT. The opposite result was obtained using the platelets from 2 patients with the Hermansky-Pudlak syndrome which contained few granules labelled by mepacrine and took up less 14C-5-HT than normal human platelets. Centrifugation of the patients' platelets on discontinuous sucrose gradients showed that the platelets of the 2 Bernard-Soulier patients were much denser than normal whereas a high proportion of low density platelets was observed in the Hermansky-Pudlak syndrome. These results further define the platelet abnormalities in the two syndromes and suggest that dense body number may be one of the factors governing platelet density.

摘要

我们已使用吖啶黄标记程序来测量2种遗传性疾病患者血小板的致密体(5-羟色胺储存细胞器)含量,这2种疾病被怀疑存在致密体数量异常。将血小板与吖啶黄一起孵育,然后通过荧光显微镜检查。从40名正常人类受试者分离的血小板所获数据计算得出,每个血小板的致密体平均数为5.4±0.8(标准差)。相比之下,2名伯纳德-苏利耶综合征患者的血小板平均含有14个和17个标记颗粒。这种增加与血小板积累14C-5-羟色胺的能力大大增强有关。使用2名赫尔曼斯基-普德拉克综合征患者的血小板得出了相反的结果,这些血小板中被吖啶黄标记的颗粒很少,并且比正常人类血小板摄取的14C-5-羟色胺更少。对患者的血小板进行不连续蔗糖梯度离心显示,2名伯纳德-苏利耶患者的血小板比正常血小板密度大得多,而在赫尔曼斯基-普德拉克综合征中观察到高比例的低密度血小板。这些结果进一步明确了这两种综合征中的血小板异常情况,并表明致密体数量可能是决定血小板密度的因素之一。

相似文献

1
Relationship between mepacrine-labelled dense body number, platelet capacity to accumulate 14C-5-HT and platelet density in the Bernard-Soulier and Hermansky-Pudlak syndromes.伯纳德-索利尔综合征和赫尔曼斯基-普德拉克综合征中,米帕林标记的致密体数量、血小板积累14C-5-羟色胺的能力与血小板密度之间的关系。
Thromb Haemost. 1979 Aug 31;42(2):694-704.
2
Mepacrine labelling test and uranaffin cytochemical reaction in human megakaryocytes.人巨核细胞中的阿的平标记试验及铀番红细胞化学反应
Thromb Haemost. 1982 Jun 28;47(3):232-5.
3
Further investigations on Bernard-Soulier platelet abnormalities.关于伯纳德-苏利耶血小板异常的进一步研究。
J Lab Clin Med. 1981 May;97(5):689-99.
4
Platelets in myeloproliferative disorders. II. Serotonin uptake and storage: correlations with mepacrine labelled dense bodies and with platelet density.骨髓增殖性疾病中的血小板。II. 5-羟色胺摄取与储存:与米帕林标记的致密体及血小板密度的相关性
Scand J Haematol. 1980 Oct;25(4):289-95.
5
Membrane defects in inherited disorders of platelet function.遗传性血小板功能障碍中的膜缺陷。
Am J Pediatr Hematol Oncol. 1982 Spring;4(1):83-94.
6
A flow cytometric assay using mepacrine for study of uptake and release of platelet dense granule contents.一种使用米帕林的流式细胞术检测法,用于研究血小板致密颗粒内容物的摄取和释放。
Br J Haematol. 1995 Feb;89(2):380-5. doi: 10.1111/j.1365-2141.1995.tb03315.x.
7
Mepacrine, a tool for investigating the 5-hydroxytryptamine organelles of blood platelets by fluorescence microscopy.米帕林,一种通过荧光显微镜研究血小板5-羟色胺细胞器的工具。
J Lab Clin Med. 1977 Jan;89(1):200-6.
8
Initial characterization of human platelet mepacrine-labelled granules isolated using a short metrizamide gradient.使用短的甲泛葡胺梯度分离的人血小板米帕林标记颗粒的初步表征。
Br J Haematol. 1982 Oct;52(2):241-51. doi: 10.1111/j.1365-2141.1982.tb03886.x.
9
Platelet dense bodies loaded with mepacrine. Study in chronic idiopathic thrombocytopenic purpura (ITP).装载有米帕林的血小板致密体。慢性特发性血小板减少性紫癜(ITP)的研究。
Thromb Haemost. 1980 Jul 15;43(3):208-10.
10
Evidence that abnormal platelet functions in human Chédiak-Higashi syndrome are the result of a lack of dense bodies.人类切-东综合征中血小板功能异常是由于致密体缺乏所致的证据。
Am J Pathol. 1983 Jun;111(3):307-14.

引用本文的文献

1
Platelet dense granules begin to selectively accumulate mepacrine during proplatelet formation.在血小板生成过程中,血小板致密颗粒开始选择性地积累米帕林。
Blood Adv. 2017 Aug 22;1(19):1478-1490. doi: 10.1182/bloodadvances.2017006726.
2
Analysis of the glycoprotein and protein composition of Bernard-Soulier platelets by single and two-dimensional sodium dodecyl sulfate-polyacrylamide gel electrophoresis.通过一维和二维十二烷基硫酸钠-聚丙烯酰胺凝胶电泳分析伯纳德-索利尔血小板的糖蛋白和蛋白质组成。
J Clin Invest. 1981 May;67(5):1431-40. doi: 10.1172/jci110172.
3
Evidence that abnormal platelet functions in human Chédiak-Higashi syndrome are the result of a lack of dense bodies.
人类切-东综合征中血小板功能异常是由于致密体缺乏所致的证据。
Am J Pathol. 1983 Jun;111(3):307-14.
4
Gray platelet syndrome: selective alpha-granule deficiency and thrombocytopenia due to increased platelet turnover.灰色血小板综合征:由于血小板周转率增加导致的选择性α颗粒缺乏和血小板减少症。
Blut. 1985 Jun;50(6):331-40. doi: 10.1007/BF00320926.