共 41 条
Evidence of CCR2-independent transmigration of Ly6Chi monocytes into the brain after permanent cerebral ischemia in mice
被引:16
作者:

Chu, Hannah X.
论文数: 0 引用数: 0
h-index: 0
机构: Monash Univ, Vasc Biol & Immunopharmacol Grp, Cardiovasc Dis Program, Biomed Discovery Inst, Wellington Rd, Clayton, Vic 3800, Australia

Kim, Hyun Ah
论文数: 0 引用数: 0
h-index: 0
机构: Monash Univ, Vasc Biol & Immunopharmacol Grp, Cardiovasc Dis Program, Biomed Discovery Inst, Wellington Rd, Clayton, Vic 3800, Australia

Lee, Seyoung
论文数: 0 引用数: 0
h-index: 0
机构: Monash Univ, Vasc Biol & Immunopharmacol Grp, Cardiovasc Dis Program, Biomed Discovery Inst, Wellington Rd, Clayton, Vic 3800, Australia

Broughton, Brad R. S.
论文数: 0 引用数: 0
h-index: 0
机构: Monash Univ, Vasc Biol & Immunopharmacol Grp, Cardiovasc Dis Program, Biomed Discovery Inst, Wellington Rd, Clayton, Vic 3800, Australia

Drummond, Grant R.
论文数: 0 引用数: 0
h-index: 0
机构: Monash Univ, Vasc Biol & Immunopharmacol Grp, Cardiovasc Dis Program, Biomed Discovery Inst, Wellington Rd, Clayton, Vic 3800, Australia

Sobey, Christopher G.
论文数: 0 引用数: 0
h-index: 0
机构:
Monash Univ, Vasc Biol & Immunopharmacol Grp, Cardiovasc Dis Program, Biomed Discovery Inst, Wellington Rd, Clayton, Vic 3800, Australia Monash Univ, Vasc Biol & Immunopharmacol Grp, Cardiovasc Dis Program, Biomed Discovery Inst, Wellington Rd, Clayton, Vic 3800, Australia
机构:
[1] Monash Univ, Vasc Biol & Immunopharmacol Grp, Cardiovasc Dis Program, Biomed Discovery Inst, Wellington Rd, Clayton, Vic 3800, Australia
来源:
基金:
澳大利亚国家健康与医学研究理事会;
英国医学研究理事会;
关键词:
CCR2;
antagonist;
Inflammation;
Ly6C(hi) monocytes;
Permanent cerebral ischemia;
Stroke;
ARTERY OCCLUSION;
BONE-MARROW;
CCR2;
STROKE;
MECHANISMS;
EXPRESSION;
TRANSIENT;
SUBSETS;
INJURY;
INFILTRATION;
D O I:
10.1016/j.brainres.2016.02.030
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
Previously we showed that INCB3344, a CCR2 antagonist, inhibits transmigration of Ly6C(hi) monocytes into the brain after ischemia-reperfusion. Here we tested the effect of CCR2 inhibition during permanent cerebral ischemia. Mice were administered either vehicle (dimethyl sulfoxide/carboxymethylcellulose) or INCB3344 (30 or 100 mg/kg IP) 1 h before middle cerebral artery occlusion and at 2 and 6 h after the initiation of ischemia. After 24 h, we assessed functional outcome, infarct volume and quantified immune cells in blood and brain. The increase in circulating bone marrow-derived Ly6Chi monocytes, but not the infiltration of those cells into the brain, was blocked by the CCR2 antagonist. INCB3344 had no effect on either neurological deficit or infarct volume. Our data confirm that cerebral ischemia triggers a CCR2-dependent increase in circulating Ly6Chi monocytes, but suggest that in the absence of reperfusion these cells may transmigrate into the ischemic brain in a CCR2-independent manner. (C) 2016 Elsevier B.V. All rights reserved.
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页码:118 / 127
页数:10
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