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血浆血管性血友病因子未掺入猪血小板α-颗粒。

Absence of incorporation of plasma von Willebrand factor into porcine platelet alpha-granules.

作者信息

Roussi J, Drouet L, Sigman J, Vaiman M, Pignaud G, Bonneau M, Masse J M, Cramer E M

机构信息

Laboratoire d'Hématologie, Hôpital Raymond Poincare, Garches, France.

出版信息

Br J Haematol. 1995 Jul;90(3):661-8. doi: 10.1111/j.1365-2141.1995.tb05598.x.

Abstract

In order to study the relationship between plasma and platelet von Willebrand factor (vWF), we used an experimental model of crossed bone marrow transplantation (BMT) between SLA immunocompatible normal and homozygous von Willebrand (vWD) pigs. A normal pig received bone marrow from a vWD pig and a second pig with vWD was engrafted with marrow from a normal pig. Each recipient, after total irradiation of 10 Grays, received by a central catheter 10(10) monocellular bone marrow cells without immunosuppression. The animals were followed for 50 d and no graft rejection or graft-versus-host disease was observed. After aplasia occurring 3 weeks after BMT, white blood cells and platelets returned to normal. Before transplantation, in the vWD pig, vWFAg and vWF activity were not detected in plasma and in platelet and megakaryocyte alpha-granules. After transplantation with normal marrow, platelet vWFAg and platelet vWF activity wer normal and high molecular weight multimers and numerous tubular structures were present in alpha-granules. Before transplantation, the normal pig had normal plasma and platelet vWFAg-vWF activity, normal multimeric pattern, and the platelet and megakaryocyte alpha-granules displayed many tubular structures, eccentrically located in one of their poles, coinciding with immunogold staining vWFAg. After transplantation with homozygous vWD marrow, platelet and megakaryocyte alpha-granules lacked tubular structures. Alpha-granule immunogold staining for vWF was consistently negative, although plasma vWF was at a normal level. In conclusion, this study shows that, unlike other plasma proteins such as fibrinogen. vWF endocytosis does not occur from plasma to the platelet alpha-granules. Platelet and megakaryocyte vWF solely originates from megakaryocyte endogenous synthesis and is independent of plasma vWF.

摘要

为了研究血浆与血小板血管性血友病因子(vWF)之间的关系,我们使用了SLA免疫相容的正常猪与纯合血管性血友病(vWD)猪之间的交叉骨髓移植(BMT)实验模型。一只正常猪接受了来自vWD猪的骨髓,另一只患有vWD的猪则移植了来自正常猪的骨髓。每只受体在接受10格雷的全身照射后,通过中心静脉导管接受10(10)个单细胞骨髓细胞,且未进行免疫抑制。对这些动物进行了50天的随访,未观察到移植物排斥或移植物抗宿主病。骨髓移植3周后出现再生障碍,之后白细胞和血小板恢复正常。移植前,vWD猪的血浆、血小板及巨核细胞α颗粒中均未检测到vWFAg和vWF活性。移植正常骨髓后,血小板vWFAg和血小板vWF活性正常,α颗粒中存在高分子量多聚体和大量管状结构。移植前,正常猪的血浆和血小板vWFAg-vWF活性正常,多聚体模式正常,血小板和巨核细胞α颗粒显示出许多管状结构,偏心位于其一个极,与免疫金染色的vWFAg一致。移植纯合vWD骨髓后,血小板和巨核细胞α颗粒缺乏管状结构。尽管血浆vWF水平正常,但vWF的α颗粒免疫金染色始终为阴性。总之,本研究表明,与纤维蛋白原等其他血浆蛋白不同,vWF不会从血浆内吞至血小板α颗粒。血小板和巨核细胞vWF仅起源于巨核细胞内源性合成,且独立于血浆vWF。

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