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骨髓嵌合体在实验性中风研究中的应用。

Bone marrow chimeras in the study of experimental stroke.

机构信息

Department of Neurology, University of California, San Francisco, San Francisco, CA, USA.

出版信息

Transl Stroke Res. 2012 Sep;3(3):341-7. doi: 10.1007/s12975-012-0169-6. Epub 2012 May 5.

DOI:10.1007/s12975-012-0169-6
PMID:24323809
Abstract

Inflammation is known to contribute to stroke evolution, and poststroke immune responses have been documented to emanate from the brain via microglia. However, circulating immune cells are increasingly recognized to play a significant role as well. Recent work has demonstrated the importance of the peripheral circulation and stroke pathogenesis. Understanding how the peripheral circulation contributes to ischemic brain injury may reveal important therapeutic targets and strategies. The use of bone marrow chimeras can be a useful tool in understanding the relative contributions of brain resident and peripheral inflammatory responses.

摘要

炎症被认为是中风演变的一个促成因素,并且已经有文献记录表明中风后的免疫反应是由小胶质细胞从大脑中发出的。然而,循环免疫细胞的作用也越来越受到重视。最近的研究表明,外周循环在中风发病机制中起着重要作用。了解外周循环如何导致缺血性脑损伤可能揭示重要的治疗靶点和策略。使用骨髓嵌合体可以成为理解大脑固有和外周炎症反应相对贡献的有用工具。

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Bone marrow chimeras in the study of experimental stroke.骨髓嵌合体在实验性中风研究中的应用。
Transl Stroke Res. 2012 Sep;3(3):341-7. doi: 10.1007/s12975-012-0169-6. Epub 2012 May 5.
2
Aging alters the immunological response to ischemic stroke.衰老改变了对缺血性中风的免疫反应。
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Ann Neurol. 2011 Oct;70(4):606-15. doi: 10.1002/ana.22476.
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FGF21 alleviates neuroinflammation following ischemic stroke by modulating the temporal and spatial dynamics of microglia/macrophages.成纤维细胞生长因子 21 通过调节小胶质细胞/巨噬细胞的时空动力学缓解缺血性脑卒中后的神经炎症。
J Neuroinflammation. 2020 Aug 31;17(1):257. doi: 10.1186/s12974-020-01921-2.
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Immune cell trafficking across the barriers of the central nervous system in multiple sclerosis and stroke.免疫细胞在多发性硬化症和中风中穿越中枢神经系统屏障的过程。
Biochim Biophys Acta. 2016 Mar;1862(3):461-71. doi: 10.1016/j.bbadis.2015.10.018. Epub 2015 Oct 23.
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[Immune responses and neuroimmune modulation in the pathogenesis of acute ischemic stroke and poststroke infections].[急性缺血性卒中发病机制及卒中后感染中的免疫反应与神经免疫调节]
Ideggyogy Sz. 2010 Jul 30;63(7-8):232-46.
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引用本文的文献

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Triggering receptor expressed on myeloid cells-2 expression in the brain is required for maximal phagocytic activity and improved neurological outcomes following experimental stroke.触发受体表达在髓样细胞-2 在大脑中的表达是实验性中风后最大吞噬活性和改善神经功能结局所必需的。
J Cereb Blood Flow Metab. 2019 Oct;39(10):1906-1918. doi: 10.1177/0271678X18817282. Epub 2018 Dec 7.
2
ST2/IL-33-Dependent Microglial Response Limits Acute Ischemic Brain Injury.ST2/白细胞介素-33依赖性小胶质细胞反应限制急性缺血性脑损伤。
J Neurosci. 2017 May 3;37(18):4692-4704. doi: 10.1523/JNEUROSCI.3233-16.2017. Epub 2017 Apr 7.
3
Functional differences between microglia and monocytes after ischemic stroke.

本文引用的文献

1
NADPH oxidase in stroke and cerebrovascular disease.中风和脑血管疾病中的NADPH氧化酶
Neurol Res. 2012 May;34(4):338-45. doi: 10.1179/1743132812Y.0000000021.
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Significance of marrow-derived nicotinamide adenine dinucleotide phosphate oxidase in experimental ischemic stroke.骨髓衍生烟酰胺腺嘌呤二核苷酸磷酸氧化酶在实验性缺血性卒中中的意义。
Ann Neurol. 2011 Oct;70(4):606-15. doi: 10.1002/ana.22476.
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Hyperglycemia promotes tissue plasminogen activator-induced hemorrhage by Increasing superoxide production.高血糖通过增加超氧化物的产生促进组织型纤溶酶原激活物诱导的出血。
缺血性中风后小胶质细胞与单核细胞的功能差异
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Targeting the peripheral inflammatory response to stroke: role of the spleen.针对中风的外周炎症反应:脾脏的作用。
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Brain arteriovenous malformation modeling, pathogenesis, and novel therapeutic targets.脑动静脉畸形建模、发病机制及新型治疗靶点
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The role of the microglia in acute CNS injury.小胶质细胞在急性中枢神经系统损伤中的作用。
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Microglia and ischemic stroke: a double-edged sword.小胶质细胞与缺血性中风:一把双刃剑。
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Ann Neurol. 2011 Oct;70(4):583-90. doi: 10.1002/ana.22538. Epub 2011 Oct 14.
4
Bone marrow-derived cells are the major source of MMP-9 contributing to blood-brain barrier dysfunction and infarct formation after ischemic stroke in mice.骨髓来源的细胞是 MMP-9 的主要来源,有助于缺血性中风后小鼠的血脑屏障功能障碍和梗死形成。
Brain Res. 2009 Oct 19;1294:183-92. doi: 10.1016/j.brainres.2009.07.070. Epub 2009 Jul 29.
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Inhibition of NADPH oxidase is neuroprotective after ischemia-reperfusion.抑制NADPH氧化酶在缺血再灌注后具有神经保护作用。
J Cereb Blood Flow Metab. 2009 Jul;29(7):1262-72. doi: 10.1038/jcbfm.2009.47. Epub 2009 May 6.
6
Effects of monocyte chemoattractant protein 1 on blood-borne cell recruitment after transient focal cerebral ischemia in mice.单核细胞趋化蛋白1对小鼠短暂性局灶性脑缺血后血源性细胞募集的影响。
Neuroscience. 2009 Jul 7;161(3):806-12. doi: 10.1016/j.neuroscience.2009.04.025. Epub 2009 Apr 15.
7
The HMGB1 receptor RAGE mediates ischemic brain damage.高迁移率族蛋白B1(HMGB1)受体晚期糖基化终末产物受体(RAGE)介导缺血性脑损伤。
J Neurosci. 2008 Nov 12;28(46):12023-12031. doi: 10.1523/JNEUROSCI.2435-08.2008.
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Apocynin improves outcome in experimental stroke with a narrow dose range.白杨素在狭窄剂量范围内可改善实验性中风的预后。
Neuroscience. 2008 Jun 23;154(2):556-62. doi: 10.1016/j.neuroscience.2008.03.090. Epub 2008 Apr 23.
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The spleen contributes to stroke-induced neurodegeneration.脾脏会导致中风引起的神经退行性变。
J Neurosci Res. 2008 Aug 1;86(10):2227-34. doi: 10.1002/jnr.21661.
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Apocynin attenuates cerebral infarction after transient focal ischaemia in rats.白杨素可减轻大鼠短暂局灶性缺血后的脑梗死。
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