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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.

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。

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