Proliferating resident microglia after focal cerebral ischaemia in mice
Denes, Adam; Vidyasagar, Rishma; Feng, Jianghua; Narvainen, Johanna; McColl, Barry W.; Kauppinen, Risto A.; Allan, Stuart M.
刊名JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM
2007-12-01
卷号27期号:12页码:1941-1953
关键词cell labelling inflammation MRI macrophages neurodegeneration
英文摘要Cerebral ischaemia usually results in the rapid death of neurons within the immediate territory of the affected artery. Neuronal loss is accompanied by a sequence of events, including brain oedema, blood-brain barrier (BBB) breakdown, and neuroinflammation, all of which contribute to further neuronal death. Although the role of macrophages and mononuclear phagocytes in the expansion of ischaemic injury has been widely studied, the relative contribution of these cells, either of exogenous or intrinsic central nervous system (CNS) origin is still not entirely clear. The purpose of this study, therefore, was to use different durations of transient middle cerebral artery occlusion (tMCAo) in the mouse to investigate fully post-occlusion BBB permeability and cellular changes in the brain during the 72 h post-MCAo period. This was achieved using in vivo magnetic resonance imaging (MRI) and cell labelling techniques. Our results show that BBB breakdown and formation of the primary ischaemic damage after tMCAo is not associated with significant infiltration of neutrophils, although more are observed with longer periods of MCAo. In addition, we observe very few infiltrating exogenous macrophages over a 72 h period after 30 or 60 mins of occlusion, instead a profound increase in proliferating resident microglia cells was observed. Interestingly, the more severe injury associated with 60 mins of MCAo leads to a markedly reduced proliferation of resident microglial cells, suggesting that these cells may play a protective function, possibly through phagocytosis of infiltrating neutrophils. These data further support possible beneficial actions of microglial cells in the injured brain.
WOS标题词Science & Technology ; Life Sciences & Biomedicine
类目[WOS]Endocrinology & Metabolism ; Hematology ; Neurosciences
研究领域[WOS]Endocrinology & Metabolism ; Hematology ; Neurosciences & Neurology
关键词[WOS]MARROW CHIMERIC MICE ; BONE-MARROW ; RAT-BRAIN ; ARTERY OCCLUSION ; HEMATOGENOUS MACROPHAGES ; INFLAMMATORY RESPONSE ; GENE-EXPRESSION ; TISSUE-DAMAGE ; STROKE ; CELLS
收录类别SCI
语种英语
WOS记录号WOS:000250957800006
公开日期2015-10-13
内容类型期刊论文
源URL[http://ir.wipm.ac.cn/handle/112942/7916]  
专题武汉物理与数学研究所_2011年以前论文发表(包括2011年)
作者单位1.Hungarian Acad Sci, Inst Expt Med, Lab Mol Neuroendocrinol, H-1083 Budapest, Hungary
2.Univ Birmingham, Sch Sport & Exercise Sci, Birmingham, W Midlands, England
3.Univ Manchester, Fac Life Sci, Michael Smith Bldg, Manchester, Lancs, England
4.Chinese Acad Sci, Wuhan Inst Phys & Math, State Key Lab Magnet Resonance & Atom & Mol Phys, Wuhan, Peoples R China
推荐引用方式
GB/T 7714
Denes, Adam,Vidyasagar, Rishma,Feng, Jianghua,et al. Proliferating resident microglia after focal cerebral ischaemia in mice[J]. JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM,2007,27(12):1941-1953.
APA Denes, Adam.,Vidyasagar, Rishma.,Feng, Jianghua.,Narvainen, Johanna.,McColl, Barry W..,...&Allan, Stuart M..(2007).Proliferating resident microglia after focal cerebral ischaemia in mice.JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM,27(12),1941-1953.
MLA Denes, Adam,et al."Proliferating resident microglia after focal cerebral ischaemia in mice".JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM 27.12(2007):1941-1953.
个性服务
查看访问统计
相关权益政策
暂无数据
收藏/分享
所有评论 (0)
暂无评论
 

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。


©版权所有 ©2017 CSpace - Powered by CSpace