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J Clin Invest. 2017 Jun 1;127(6):2040-2043. doi: 10.1172/JCI94494. Epub 2017 May 15.
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Thrombocytosis in an infant with high thrombopoietin concentrations.血小板生成素浓度高的婴儿出现血小板增多症。
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本文引用的文献

1
Neutrophil-derived S100 calcium-binding proteins A8/A9 promote reticulated thrombocytosis and atherogenesis in diabetes.中性粒细胞衍生的S100钙结合蛋白A8/A9促进糖尿病中的网状血小板增多和动脉粥样硬化。
J Clin Invest. 2017 Jun 1;127(6):2133-2147. doi: 10.1172/JCI92450. Epub 2017 May 15.
2
Newly Formed Reticulated Platelets Undermine Pharmacokinetically Short-Lived Antiplatelet Therapies.新形成的网状血小板会削弱药代动力学半衰期短的抗血小板疗法。
Arterioscler Thromb Vasc Biol. 2017 May;37(5):949-956. doi: 10.1161/ATVBAHA.116.308763. Epub 2017 Mar 9.
3
Heart Disease and Stroke Statistics-2017 Update: A Report From the American Heart Association.《2017年心脏病和中风统计数据更新:美国心脏协会报告》
Circulation. 2017 Mar 7;135(10):e146-e603. doi: 10.1161/CIR.0000000000000485. Epub 2017 Jan 25.
4
S100A8/A9: From basic science to clinical application.S100A8/A9:从基础科学到临床应用。
Pharmacol Ther. 2016 Nov;167:120-131. doi: 10.1016/j.pharmthera.2016.07.015. Epub 2016 Aug 1.
5
Impact of reticulated platelets on antiplatelet response to thienopyridines is independent of platelet turnover.网织血小板对噻吩吡啶类抗血小板反应的影响与血小板更新无关。
Thromb Haemost. 2016 Oct 28;116(5):941-948. doi: 10.1160/TH16-03-0191. Epub 2016 Aug 4.
6
Impact of diabetes on immature platelets fraction and its relationship with platelet reactivity in patients receiving dual antiplatelet therapy.糖尿病对接受双联抗血小板治疗患者未成熟血小板分数的影响及其与血小板反应性的关系。
J Thromb Thrombolysis. 2016 Aug;42(2):245-53. doi: 10.1007/s11239-016-1348-1.
7
Novel mechanisms of platelet clearance and thrombopoietin regulation.血小板清除和血小板生成素调节的新机制。
Curr Opin Hematol. 2015 Sep;22(5):445-51. doi: 10.1097/MOH.0000000000000170.
8
Altered platelets' morphological parameters in children with type 1 diabetes – a case-control study.1型糖尿病患儿血小板形态学参数的改变——一项病例对照研究。
BMC Endocr Disord. 2015 Apr 3;15:17. doi: 10.1186/s12902-015-0011-8.
9
Adipose tissue macrophages promote myelopoiesis and monocytosis in obesity.脂肪组织巨噬细胞促进肥胖症中的骨髓细胞生成和单核细胞增多。
Cell Metab. 2014 May 6;19(5):821-35. doi: 10.1016/j.cmet.2014.03.029.
10
Hyperglycemia promotes myelopoiesis and impairs the resolution of atherosclerosis.高血糖促进骨髓生成,并损害动脉粥样硬化的消退。
Cell Metab. 2013 May 7;17(5):695-708. doi: 10.1016/j.cmet.2013.04.001.

糖使中性粒细胞产生晚期糖基化终末产物:将糖尿病相关的高血糖与血小板增多症和血小板反应性联系起来。

Sugar makes neutrophils RAGE: linking diabetes-associated hyperglycemia to thrombocytosis and platelet reactivity.

作者信息

Lee Robert H, Bergmeier Wolfgang

机构信息

McAllister Heart Institute and.

Department of Biochemistry and Biophysics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.

出版信息

J Clin Invest. 2017 Jun 1;127(6):2040-2043. doi: 10.1172/JCI94494. Epub 2017 May 15.

DOI:10.1172/JCI94494
PMID:28504654
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5451221/
Abstract

Diabetes mellitus is associated with an increased risk for cardiovascular disease, but the link between hyperglycemia and atherothrombotic disease is not completely understood. Patients with diabetes often show hyporesponsiveness to antiplatelet therapies, and it has been suggested that hyperreactive reticulated platelets underlie this altered therapeutic response. In this issue of the JCI, Kraakman et al. uncover a previously unknown link between hyperglycemia and enhanced platelet production and reactivity. The authors demonstrate that high blood glucose levels trigger neutrophil release of S100 calcium-binding protein A8/A9 (S100A8/A9), which binds to the receptor for advanced glycation end products (RAGE) on Kupffer cells, ultimately leading to increased thrombopoietin (TPO) production in the liver. TPO causes megakaryocyte proliferation and increased platelet production. This study demonstrates the importance of glycemic control and identifies potential therapeutic targets in the normalization of platelet numbers and function in diabetes.

摘要

糖尿病与心血管疾病风险增加相关,但高血糖与动脉粥样硬化血栓形成性疾病之间的联系尚未完全明确。糖尿病患者对抗血小板治疗往往反应低下,有人提出高反应性网织血小板是这种治疗反应改变的基础。在本期《临床研究杂志》中,克拉阿克曼等人发现了高血糖与血小板生成增加及反应性增强之间此前未知的联系。作者证明,高血糖水平会触发中性粒细胞释放S100钙结合蛋白A8/A9(S100A8/A9),该蛋白与库普弗细胞上的晚期糖基化终产物受体(RAGE)结合,最终导致肝脏中血小板生成素(TPO)产生增加。TPO会引起巨核细胞增殖并增加血小板生成。这项研究证明了血糖控制的重要性,并确定了使糖尿病患者血小板数量和功能恢复正常的潜在治疗靶点。