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磷脂酰丝氨酸阳性微粒可改善血友病 A 血浆模型的体外止血功能。

Phosphatidylserine positive microparticles improve hemostasis in in-vitro hemophilia A plasma models.

机构信息

Department of Molecular Medicine & Surgery, Karolinska Institutet, Stockholm, Sweden.

Department of Medicine, Division of Rheumatology, Karolinska Institutet, Stockholm, Sweden.

出版信息

Sci Rep. 2020 May 12;10(1):7871. doi: 10.1038/s41598-020-64686-x.

Abstract

Circulating microparticles (MPs) are procoagulant due to the surface containing phosphatidylserine (PS), which facilitates coagulation. We investigated if MPs improve hemostasis in HA plasma models. MPs isolated from pooled normal human plasma were added to severe, moderate and mild HA plasma models (0%, 2.5%, 20% FVIII). The MPs' effect on hemostasis was evaluated by calibrated automated thrombogram (CAT) and overall hemostasis potential (OHP) assays, while fibrin structure was imaged by standard confocal, stimulated emission depletion (STED) microscopy and scanning electron microscopy (SEM). MPs partially restored thrombin generation and fibrin formation in all HA plasma models. The procoagulant effect of MPs requires PS exposure, to a less extent of contact pathway activation, but not tissue factor exposure or in vitro stimulation of MPs. MPs partially normalized the fibrin structure, and using super-resolution STED, MPs attached to fibrin were clearly resolved. In summary, our results demonstrate that PS positive MPs could improve hemostasis in HA plasma models.

摘要

循环微颗粒(MPs)由于表面含有磷脂酰丝氨酸(PS)而具有促凝作用,这有助于凝血。我们研究了 MPs 是否能改善 HA 血浆模型中的止血功能。从混合正常人体血浆中分离出的 MPs 添加到严重、中度和轻度 HA 血浆模型(0%、2.5%、20%VIII 因子)中。通过校准自动血栓图(CAT)和整体止血潜力(OHP)测定来评估 MPs 对止血的影响,同时通过标准共焦、受激发射损耗(STED)显微镜和扫描电子显微镜(SEM)来成像纤维蛋白结构。 MPs 部分恢复了所有 HA 血浆模型中的凝血酶生成和纤维蛋白形成。 MPs 的促凝作用需要 PS 暴露,在一定程度上需要接触途径激活,但不需要组织因子暴露或 MPs 的体外刺激。 MPs 部分使纤维蛋白结构正常化,并且使用超分辨率 STED,附着在纤维蛋白上的 MPs 可以被清晰地分辨出来。总之,我们的结果表明,PS 阳性 MPs 可以改善 HA 血浆模型中的止血功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ca6/7217932/7f7b61fa7023/41598_2020_64686_Fig1_HTML.jpg

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