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颗粒胞吐对于血小板铺展是必需的:表达 VAMP-7 的α 颗粒的差异分拣。

Granule exocytosis is required for platelet spreading: differential sorting of α-granules expressing VAMP-7.

机构信息

Division of Hemostasis and Thrombosis, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215, USA.

出版信息

Blood. 2012 Jul 5;120(1):199-206. doi: 10.1182/blood-2011-10-389247. Epub 2012 May 15.

Abstract

There has been recent controversy as to whether platelet α-granules represent a single granule population or are composed of different subpopulations that serve discrete functions. To address this question, we evaluated the localization of vesicle-associated membrane proteins (VAMPs) in spread platelets to determine whether platelets actively sort a specific subpopulation of α-granules to the periphery during spreading. Immunofluorescence microscopy demonstrated that granules expressing VAMP-3 and VAMP-8 localized to the central granulomere of spread platelets along with the granule cargos von Willebrand factor and serotonin. In contrast, α-granules expressing VAMP-7 translocated to the periphery of spread platelets along with the granule cargos TIMP2 and VEFG. Time-lapse microscopy demonstrated that α-granules expressing VAMP-7 actively moved from the granulomere to the periphery during spreading. Platelets from a patient with gray platelet syndrome lacked α-granules and demonstrated only minimal spreading. Similarly, spreading was impaired in platelets obtained from Unc13d(Jinx) mice, which are deficient in Munc13-4 and have an exocytosis defect. These studies identify a new α-granule subtype expressing VAMP-7 that moves to the periphery during spreading, supporting the premise that α-granules are heterogeneous and demonstrating that granule exocytosis is required for platelet spreading.

摘要

最近有争议认为血小板α颗粒是单一颗粒群体还是由不同的亚群组成,这些亚群具有不同的功能。为了解决这个问题,我们评估了扩展血小板中囊泡相关膜蛋白(VAMPs)的定位,以确定在扩展过程中血小板是否主动将特定的α颗粒亚群分拣到外周。免疫荧光显微镜显示,表达 VAMP-3 和 VAMP-8 的颗粒与血小板颗粒载体 von Willebrand 因子和 5-羟色胺一起定位于扩展血小板的中央颗粒区。相比之下,表达 VAMP-7 的α颗粒与血小板颗粒载体 TIMP2 和 VEFG 一起向扩展血小板的外周转移。延时显微镜显示,表达 VAMP-7 的α颗粒在扩展过程中主动从颗粒区向外周移动。灰色血小板综合征患者的血小板缺乏α颗粒,仅显示最小程度的扩展。同样,UNC13D(Jinx)小鼠来源的血小板(UNC13D 基因敲除)的扩散受到损害,UNC13D 基因敲除会导致 Munc13-4 缺乏,从而导致胞吐作用缺陷。这些研究确定了一种新的表达 VAMP-7 的α颗粒亚型,该亚型在扩展过程中向外周移动,支持了α颗粒具有异质性的前提,并证明了颗粒胞吐作用是血小板扩展所必需的。

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