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A statin-based inhibitor of lymphocyte function antigen-1 protects against ischemia/reperfusion-induced leukocyte adhesion in the colon.一种基于他汀类药物的淋巴细胞功能相关抗原-1抑制剂可预防结肠缺血/再灌注诱导的白细胞黏附。
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2
Fundamental and distinct roles of P-selectin and LFA-1 in ischemia/reperfusion-induced leukocyte-endothelium interactions in the mouse colon.P-选择素和淋巴细胞功能相关抗原-1在小鼠结肠缺血/再灌注诱导的白细胞-内皮细胞相互作用中的基本且独特作用
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Role of angiotensin II in ischemia/reperfusion-induced leukocyte-endothelium interactions in the colon.血管紧张素II在结肠缺血/再灌注诱导的白细胞与内皮细胞相互作用中的作用。
FASEB J. 2004 May;18(7):881-3. doi: 10.1096/fj.03-0502fje. Epub 2004 Mar 4.
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P-selectin glycoprotein ligand-1 regulates chemokine-dependent leukocyte recruitment in colonic ischemia-reperfusion.P-选择素糖蛋白配体-1调节结肠缺血再灌注中趋化因子依赖性白细胞募集。
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Rho-kinase signalling regulates CXC chemokine formation and leukocyte recruitment in colonic ischemia-reperfusion.Rho-kinase 信号通路调节结肠缺血再灌注中的 CXC 趋化因子形成和白细胞募集。
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Mast-cell-dependent secretion of CXC chemokines regulates ischemia-reperfusion-induced leukocyte recruitment in the colon.肥大细胞依赖性CXC趋化因子的分泌调节结肠缺血再灌注诱导的白细胞募集。
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Statins inhibit lymphocyte homing to peripheral lymph nodes.他汀类药物可抑制淋巴细胞归巢至外周淋巴结。
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Statins inhibit lymphocyte homing to peripheral lymph nodes.他汀类药物可抑制淋巴细胞归巢至外周淋巴结。
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Lymphocyte function antigen-1 mediates leukocyte adhesion and subsequent liver damage in endotoxemic mice.淋巴细胞功能抗原-1介导内毒素血症小鼠的白细胞黏附及随后的肝损伤。
Br J Pharmacol. 2004 Feb;141(4):709-16. doi: 10.1038/sj.bjp.0705634. Epub 2004 Jan 26.

本文引用的文献

1
Fundamental and distinct roles of P-selectin and LFA-1 in ischemia/reperfusion-induced leukocyte-endothelium interactions in the mouse colon.P-选择素和淋巴细胞功能相关抗原-1在小鼠结肠缺血/再灌注诱导的白细胞-内皮细胞相互作用中的基本且独特作用
Ann Surg. 2002 Dec;236(6):777-84; discussion 784. doi: 10.1097/00000658-200212000-00010.
2
Allopurinol and superoxide dismutase protect against leucocyte-endothelium interactions in a novel model of colonic ischaemia-reperfusion.在一种新的结肠缺血再灌注模型中,别嘌呤醇和超氧化物歧化酶可防止白细胞与内皮细胞相互作用。
Br J Surg. 2002 Dec;89(12):1572-80. doi: 10.1046/j.1365-2168.2002.02279.x.
3
Transition from rolling to firm adhesion is regulated by the conformation of the I domain of the integrin lymphocyte function-associated antigen-1.从滚动到牢固黏附的转变受整合素淋巴细胞功能相关抗原-1的I结构域构象调控。
J Biol Chem. 2002 Dec 27;277(52):50255-62. doi: 10.1074/jbc.M209822200. Epub 2002 Oct 3.
4
Statins as anti-inflammatory agents.他汀类药物作为抗炎剂。
Trends Pharmacol Sci. 2002 Oct;23(10):482-6. doi: 10.1016/s0165-6147(02)02077-1.
5
Integrins: bidirectional, allosteric signaling machines.整合素:双向变构信号传导机器
Cell. 2002 Sep 20;110(6):673-87. doi: 10.1016/s0092-8674(02)00971-6.
6
Chemokines, their receptors, and transplant outcome.趋化因子、其受体与移植结果。
Transplantation. 2002 Jul 27;74(2):149-55. doi: 10.1097/00007890-200207270-00001.
7
Leukocyte recruitment in hepatic injury: selectin-mediated leukocyte rolling is a prerequisite for CD18-dependent firm adhesion.肝损伤中的白细胞募集:选择素介导的白细胞滚动是CD18依赖性牢固黏附的前提条件。
J Hepatol. 2002 Jan;36(1):53-9. doi: 10.1016/s0168-8278(01)00226-4.
8
Small molecule inhibitors induce conformational changes in the I domain and the I-like domain of lymphocyte function-associated antigen-1. Molecular insights into integrin inhibition.小分子抑制剂可诱导淋巴细胞功能相关抗原-1的I结构域和类I结构域发生构象变化。整合素抑制的分子见解。
J Biol Chem. 2002 Mar 22;277(12):10590-8. doi: 10.1074/jbc.M110521200. Epub 2002 Jan 7.
9
Control of leukocyte rolling velocity in TNF-alpha-induced inflammation by LFA-1 and Mac-1.通过淋巴细胞功能相关抗原-1(LFA-1)和巨噬细胞抗原-1(Mac-1)对肿瘤坏死因子-α(TNF-α)诱导炎症中白细胞滚动速度的调控
Blood. 2002 Jan 1;99(1):336-41. doi: 10.1182/blood.v99.1.336.
10
Statins selectively inhibit leukocyte function antigen-1 by binding to a novel regulatory integrin site.他汀类药物通过与一个新的调节性整合素位点结合,选择性抑制白细胞功能抗原-1。
Nat Med. 2001 Jun;7(6):687-92. doi: 10.1038/89058.

一种基于他汀类药物的淋巴细胞功能相关抗原-1抑制剂可预防结肠缺血/再灌注诱导的白细胞黏附。

A statin-based inhibitor of lymphocyte function antigen-1 protects against ischemia/reperfusion-induced leukocyte adhesion in the colon.

作者信息

Wan Min Xiu, Schramm Rene, Klintman Daniel, Welzenbach Karl, Weitz-Schmidt Gabriele, Thorlacius Henrik

机构信息

Department of Surgery, Malmö University Hospital, Lund University, Malmö S- 205 02, Sweden.

出版信息

Br J Pharmacol. 2003 Sep;140(2):395-401. doi: 10.1038/sj.bjp.0705432. Epub 2003 Aug 26.

DOI:10.1038/sj.bjp.0705432
PMID:12970101
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1574028/
Abstract
  1. Statins are mainly used to control hypercholesterolemia; however, recent studies have also ascribed anti-inflammatory effects to the statins. LFA703 is a novel statin-derived compound, which potently inhibits lymphocyte function antigen-1 (LFA-1, CD11a/CD18) but does not affect HMG-CoA reductase activity. 2. The objective of this study was to examine the anti-inflammatory mechanisms of LFA703 in ischemia/reperfusion (I/R)-induced leukocyte-endothelium interactions in the colon. For this purpose, the superior mesenteric artery was occluded for 30 min and leukocyte responses were analyzed in colonic venules after 120 min of reperfusion in mice using inverted intravital fluorescence microscopy. 3. First, the inhibitory mechanisms of LFA703 on leukocyte adhesion were investigated in vitro using a mouse CD4+8+ thymocyte cell line. Immunoneutralization of LFA-1 and ICAM-1 abolished leukocyte adhesion, whereas inhibition of VLA-4 had no effect in this in vitro assay. Indeed, it was found that LFA703 dose-dependently reduced LFA-1-dependent leukocyte adhesion to mouse endothelial cells in vitro with an IC50 of 3.2 microm. 4. I/R caused an increase in leukocyte rolling and adhesion in colonic venules. Immunoneutralization of LFA-1 significantly reduced I/R-induced leukocyte adhesion by 89% in colonic venules. In contrast, I/R-provoked leukocyte rolling was insensitive to inhibition of LFA-1 function. 5. Administration of 30 mg kg-1 of LFA703 decreased reperfusion-induced leukocyte adhesion by more than 91%, while the level of leukocyte rolling was unchanged, suggesting that LFA703 effectively blocked LFA-1-dependent firm adhesion of leukocyte in the colon. However, LFA703 did not decrease the expression of LFA-1 on circulating leukocytes. 6. This study demonstrates that LFA-1 is indeed a critical adhesion molecule in mediating postischemic leukocyte adhesion in the colon. Moreover, this is the first study showing that a statin-based synthetic compound has the capacity to abolish LFA-1-dependent leukocyte adhesion in I/R. These novel findings may have great implications in the clinical treatment of conditions associated with I/R-induced tissue injury, such as organ transplantation, trauma and major surgery.
摘要
  1. 他汀类药物主要用于控制高胆固醇血症;然而,最近的研究也认为他汀类药物具有抗炎作用。LFA703是一种新型的他汀类衍生化合物,它能有效抑制淋巴细胞功能抗原-1(LFA-1,CD11a/CD18),但不影响HMG-CoA还原酶活性。2. 本研究的目的是探讨LFA703在缺血/再灌注(I/R)诱导的结肠白细胞-内皮细胞相互作用中的抗炎机制。为此,将小鼠肠系膜上动脉闭塞30分钟,并在再灌注120分钟后,使用倒置活体荧光显微镜分析结肠小静脉中的白细胞反应。3. 首先,使用小鼠CD4+8+胸腺细胞系在体外研究LFA703对白细胞黏附的抑制机制。LFA-1和ICAM-1的免疫中和消除了白细胞黏附,而在该体外试验中,抑制VLA-4没有效果。事实上,发现LFA703在体外剂量依赖性地降低了依赖LFA-1的白细胞与小鼠内皮细胞的黏附,IC50为3.2微米。4. I/R导致结肠小静脉中白细胞滚动和黏附增加。LFA-1的免疫中和显著降低了I/R诱导的结肠小静脉中白细胞黏附89%。相反,I/R引起的白细胞滚动对LFA-1功能抑制不敏感。5. 给予30mg/kg的LFA703可使再灌注诱导的白细胞黏附减少91%以上,而白细胞滚动水平未改变,这表明LFA703有效地阻断了结肠中依赖LFA-1的白细胞牢固黏附。然而,LFA703并没有降低循环白细胞上LFA-1的表达。6. 本研究表明,LFA-1确实是介导结肠缺血后白细胞黏附的关键黏附分子。此外,这是第一项表明基于他汀类的合成化合物有能力消除I/R中依赖LFA-1的白细胞黏附的研究。这些新发现可能对与I/R诱导的组织损伤相关疾病的临床治疗有重大意义,如器官移植、创伤和大手术。