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Platelets release matrix metalloproteinase-2 in the coronary circulation of patients with acute coronary syndromes: possible role in sustained platelet activation.血小板在急性冠脉综合征患者的冠状动脉循环中释放基质金属蛋白酶-2:在持续血小板激活中的可能作用。
Eur Heart J. 2011 Feb;32(3):316-25. doi: 10.1093/eurheartj/ehq390. Epub 2010 Oct 28.
2
Platelet transcriptional profile and protein expression in patients with systemic lupus erythematosus: up-regulation of the type I interferon system is strongly associated with vascular disease.系统性红斑狼疮患者的血小板转录谱和蛋白表达:I 型干扰素系统的上调与血管疾病强烈相关。
Blood. 2010 Sep 16;116(11):1951-7. doi: 10.1182/blood-2010-03-274605. Epub 2010 Jun 10.
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The platelet interior revisited: electron tomography reveals tubular alpha-granule subtypes.血小板内部再探:电子断层成像揭示管状α-颗粒亚型。
Blood. 2010 Aug 19;116(7):1147-56. doi: 10.1182/blood-2010-02-268680. Epub 2010 May 3.
4
De novo protein synthesis in mature platelets: a consideration for transfusion medicine.成熟血小板中的从头蛋白质合成:对输血医学的考虑。
Vox Sang. 2010 Aug 1;99(2):112-22. doi: 10.1111/j.1423-0410.2010.01333.x. Epub 2010 Mar 21.
5
Loss of matrix metalloproteinase 2 in platelets reduces arterial thrombosis in vivo.血小板中基质金属蛋白酶2的缺失可减少体内动脉血栓形成。
J Exp Med. 2009 Oct 26;206(11):2365-79. doi: 10.1084/jem.20090687. Epub 2009 Oct 5.
6
Existence of a microRNA pathway in anucleate platelets.无核血小板中微小RNA通路的存在。
Nat Struct Mol Biol. 2009 Sep;16(9):961-6. doi: 10.1038/nsmb.1651. Epub 2009 Aug 9.
7
Selective sorting of alpha-granule proteins.α-颗粒蛋白的选择性分选
J Thromb Haemost. 2009 Jul;7 Suppl 1(Suppl 1):173-6. doi: 10.1111/j.1538-7836.2009.03387.x.
8
Tissue inhibitors of matrix metalloproteinases in platelets and megakaryocytes: a novel organization for these secreted proteins.血小板和巨核细胞中的基质金属蛋白酶组织抑制剂:这些分泌蛋白的一种新组织形式。
Exp Hematol. 2009 Jul;37(7):849-56. doi: 10.1016/j.exphem.2009.03.009. Epub 2009 May 3.
9
PAF-acetylhydrolase expressed during megakaryocyte differentiation inactivates PAF-like lipids.在巨核细胞分化过程中表达的血小板活化因子乙酰水解酶可使类血小板活化因子脂质失活。
Blood. 2009 Jun 25;113(26):6699-706. doi: 10.1182/blood-2008-11-186312. Epub 2009 Apr 24.
10
Platelet matrix metalloprotease-1 mediates thrombogenesis by activating PAR1 at a cryptic ligand site.血小板基质金属蛋白酶-1通过在隐蔽配体位点激活PAR1来介导血栓形成。
Cell. 2009 Apr 17;137(2):332-43. doi: 10.1016/j.cell.2009.02.018.

巨核细胞将基质金属蛋白酶及其抑制剂的 mRNA 有差异地分拣到血小板中:一种调节合成事件的机制。

Megakaryocytes differentially sort mRNAs for matrix metalloproteinases and their inhibitors into platelets: a mechanism for regulating synthetic events.

机构信息

Division of Internal and Cardiovascular Medicine, Department of Internal Medicine, University of Perugia, Perugia, Italy.

出版信息

Blood. 2011 Aug 18;118(7):1903-11. doi: 10.1182/blood-2010-12-324517. Epub 2011 May 31.

DOI:10.1182/blood-2010-12-324517
PMID:21628401
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3158719/
Abstract

Megakaryocytes transfer a diverse and functional transcriptome to platelets during the final stages of thrombopoiesis. In platelets, these transcripts reflect the expression of their corresponding proteins and, in some cases, serve as a template for translation. It is not known, however, if megakaryocytes differentially sort mRNAs into platelets. Given their critical role in vascular remodeling and inflammation, we determined whether megakaryocytes selectively dispense transcripts for matrix metalloproteinases (MMPs) and their tissue inhibitors (TIMPs) into platelets. Next-generation sequencing (RNA-Seq) revealed that megakaryocytes express mRNA for 10 of the 24 human MMP family members. mRNA for all of these MMPs are present in platelets with the exception of MMP-2, 14, and 15. Megakaryocytes and platelets also express mRNA for TIMPs 1-3, but not TIMP-4. mRNA expression patterns predicted the presence and, in most cases, the abundance of each corresponding protein. Nonetheless, exceptions were observed: MMP-2 protein is present in platelets but not its transcript. In contrast, quiescent platelets express TIMP-2 mRNA but only traces of TIMP-2 protein. In response to activating signals, however, platelets synthesize significant amounts of TIMP-2 protein. These results demonstrate that megakaryocytes differentially express mRNAs for MMPs and TIMPs and selectively transfer a subset of these into platelets. Among the platelet messages, TIMP-2 serves as a template for signal-dependent translation.

摘要

巨核细胞在血小板生成的最后阶段将多样化且功能齐全的转录组转移到血小板中。在血小板中,这些转录本反映了其相应蛋白质的表达,在某些情况下,还可以作为翻译的模板。然而,巨核细胞是否会将 mRNAs 有差异地分拣到血小板中尚不清楚。鉴于它们在血管重塑和炎症中的关键作用,我们确定巨核细胞是否会选择性地将基质金属蛋白酶(MMPs)及其组织抑制剂(TIMPs)的转录本分配到血小板中。下一代测序(RNA-Seq)显示,巨核细胞表达 24 个人类 MMP 家族成员中的 10 种 mRNA。除 MMP-2、14 和 15 外,所有这些 MMP 的 mRNA 均存在于血小板中。巨核细胞和血小板还表达 TIMP-1-3 的 mRNA,但不表达 TIMP-4。mRNA 表达模式预测了每种相应蛋白质的存在和在大多数情况下的丰度。尽管如此,还是观察到了例外情况:MMP-2 蛋白存在于血小板中,但不存在其转录本。相比之下,静止的血小板表达 TIMP-2 mRNA,但仅存在痕量的 TIMP-2 蛋白。然而,在受到激活信号刺激后,血小板会合成大量的 TIMP-2 蛋白。这些结果表明,巨核细胞会有差异地表达 MMPs 和 TIMPs 的 mRNAs,并将其中一部分有选择地转移到血小板中。在血小板的信息中,TIMP-2 可作为信号依赖性翻译的模板。