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血小板因子XI:血小板激活后的细胞内定位及mRNA剪接

Platelet factor XI: intracellular localization and mRNA splicing following platelet activation.

作者信息

Zucker M, Hauschner H, Seligsohn U, Rosenberg N

机构信息

The Amalia Biron Research Institute of Thrombosis and Hemostasis, Chaim Sheba Medical Center, Tel-Hashomer and Sackler Faculty of Medicine, Tel Aviv University, Israel.

The Amalia Biron Research Institute of Thrombosis and Hemostasis, Chaim Sheba Medical Center, Tel-Hashomer and Sackler Faculty of Medicine, Tel Aviv University, Israel.

出版信息

Blood Cells Mol Dis. 2018 Mar;69:30-37. doi: 10.1016/j.bcmd.2017.04.006. Epub 2017 Apr 21.

Abstract

BACKGROUND

The structure and function of platelet factor XI (FXI) protein and the presence of F11 mRNA in platelets are controversial. Although platelets are anucleated cells they contain spliceosome components and pre-mRNAs. Three platelet proteins have been demonstrated to be spliced upon platelet activation.

OBJECTIVE

To determine whether FXI is also spliced upon activation and to discern the localization of FXI in platelets.

METHODS

Localization of FXI in platelets was assessed by confocal immunofluorescence staining. ELISA, chromogenic assay and western blot analyses were used to measure antigen levels, activity levels and size of FXI in platelets, respectively. Splicing patterns of F11 mRNA were assessed in three states of platelet activation: activated platelets, resting platelets and αIIbβ3-integrin activated platelets.

RESULTS

Platelet FXI was exhibited in platelet granules. Activated platelets exhibited higher levels of mature F11 mRNA and protein and lower levels of F11 pre-mRNA compared to resting or αIIbβ3-integrin activated platelets.

CONCLUSIONS

We confirmed the presence of FXI in platelets and showed that it is localized in granules but is not restricted to the same α-granule subtype as von-Willebrand factor and p-selectin. Our study also shows that F11 is present in platelets as pre-mRNA and is spliced upon platelet activation.

摘要

背景

血小板因子 XI(FXI)蛋白的结构与功能以及血小板中 F11 mRNA 的存在情况存在争议。尽管血小板是无核细胞,但它们含有剪接体成分和前体 mRNA。已有三种血小板蛋白被证明在血小板激活时会发生剪接。

目的

确定 FXI 在激活时是否也会发生剪接,并辨别 FXI 在血小板中的定位。

方法

通过共聚焦免疫荧光染色评估 FXI 在血小板中的定位。分别使用 ELISA、显色测定法和蛋白质印迹分析来测量血小板中 FXI 的抗原水平、活性水平和大小。在血小板激活的三种状态下评估 F11 mRNA 的剪接模式:激活的血小板、静息血小板和 αIIbβ3 整合素激活的血小板。

结果

血小板 FXI 存在于血小板颗粒中。与静息或 αIIbβ3 整合素激活的血小板相比,激活的血小板中成熟 F11 mRNA 和蛋白水平更高,而 F11 前体 mRNA 水平更低。

结论

我们证实了血小板中存在 FXI,并表明它定位于颗粒中,但不限于与血管性血友病因子和 p-选择素相同的 α 颗粒亚型。我们的研究还表明,F11 在血小板中以前体 mRNA 的形式存在,并在血小板激活时发生剪接。

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