The spleen contributes to stroke-induced neurodegeneration

被引:223
作者
Ajmo, Craig T., Jr. [2 ]
Vernon, Dionne O. L. [2 ]
Collier, Lisa [2 ]
Hall, Aaron A. [2 ]
Garbuzova-Davis, Svitlana [1 ,3 ]
Willing, Alison [1 ,3 ]
Pennypacker, Keith R. [2 ]
机构
[1] Univ S Florida, Dept Neurosurg, Tampa, FL 33216 USA
[2] Univ S Florida, Dept Mol Pharmacol & Physiol, Tampa, FL 33216 USA
[3] Univ S Florida, Ctr Excellence Aging & Brain Repair, Tampa, FL 33216 USA
关键词
stroke; spleen; neurodegeneration; inflammation; ischemia;
D O I
10.1002/jnr.21661
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Stroke, a cerebrovascular injury, is the leading cause of disability and third leading cause of death in the world. Recent reports indicate that inhibiting the inflammatory response to stroke enhances neurosurvival and limits expansion of the infarction. The immune response that is initiated in the spleen has been linked to the systemic inflammatory response to stroke, contributing to neurodegeneration. Here we show that removal of the spleen significantly reduces neurodegeneration after ischemic insult. Rats splenectomized 2 weeks before permanent middle cerebral artery occlusion had a > 80% decrease in infarction volume in the brain compared with those rats that were Subjected to the stroke surgery alone. Splenectomy also resulted in decreased numbers of activated microglia, macrophages, and neutrophils present in the brain tissue. Our results demonstrate that the peripheral immune response as mediated by the spleen is a major contributor to the inflammation that enhances neurodegeneration after stroke. (c) 2008 Wiley-Liss, Inc.
引用
收藏
页码:2227 / 2234
页数:8
相关论文
共 45 条
[1]   Inflammatory mediators and modulation of blood-brain barrier permeability [J].
Abbott, NJ .
CELLULAR AND MOLECULAR NEUROBIOLOGY, 2000, 20 (02) :131-147
[2]   Transient forebrain ischemia increases the blood-brain barrier permeability for albumin in stroke-prone spontaneously hypertensive rats [J].
Abrahám, CS ;
Harada, N ;
Deli, MA ;
Niwa, M .
CELLULAR AND MOLECULAR NEUROBIOLOGY, 2002, 22 (04) :455-462
[3]   Dynamics of polymorphonuclear leukocyte accumulation in acute cerebral infarction and their correlation with brain tissue damage [J].
Akopov, SE ;
Simonian, NA ;
Grigorian, GS .
STROKE, 1996, 27 (10) :1739-1743
[4]   Inflammation in central nervous system injury [J].
Allan, SM ;
Rothwell, NJ .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 2003, 358 (1438) :1669-1677
[5]   TIME-RELATED CHANGES IN MYELOPEROXIDASE ACTIVITY AND LEUKOTRIENE B-4 RECEPTOR-BINDING REFLECT LEUKOCYTE INFLUX IN CEREBRAL FOCAL STROKE [J].
BARONE, FC ;
HILLEGASS, LM ;
TZIMAS, MN ;
SCHMIDT, DB ;
FOLEY, JJ ;
WHITE, RF ;
PRICE, WJ ;
FEUERSTEIN, GZ ;
CLARK, RK ;
GRISWOLD, DE ;
SARAU, HM .
MOLECULAR AND CHEMICAL NEUROPATHOLOGY, 1995, 24 (01) :13-30
[6]   Inflammatory mediators and stroke: New opportunities for novel therapeutics [J].
Barone, FC ;
Feuerstein, GZ .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1999, 19 (08) :819-834
[7]   Therapeutic immunization protects dopaminergic neurons in a mouse model of Parkinson's disease [J].
Benner, EJ ;
Mosley, RL ;
Destache, CJ ;
Lewis, TB ;
Jackson-Lewis, V ;
Gorantla, S ;
Nemachek, C ;
Green, SR ;
Przedborski, S ;
Gendelman, HE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (25) :9435-9440
[8]   ANTI-CD11B MONOCLONAL-ANTIBODY REDUCES ISCHEMIC CELL-DAMAGE AFTER TRANSIENT FOCAL CEREBRAL-ISCHEMIA IN RAT [J].
CHEN, H ;
CHOPP, M ;
ZHANG, RL ;
BODZIN, G ;
CHEN, Q ;
RUSCHE, JR ;
TODD, RF .
ANNALS OF NEUROLOGY, 1994, 35 (04) :458-463
[9]   POSTISCHEMIC ADMINISTRATION OF AN ANTI-MAC-1 ANTIBODY REDUCES ISCHEMIC CELL-DAMAGE AFTER TRANSIENT MIDDLE CEREBRAL-ARTERY OCCLUSION IN RATS [J].
CHOPP, M ;
ZHANG, RL ;
CHEN, H ;
LI, Y ;
JIANG, N ;
RUSCHE, JR .
STROKE, 1994, 25 (04) :869-875
[10]   Pathobiology of ischaemic stroke: an integrated view [J].
Dirnagl, U ;
Iadecola, C ;
Moskowitz, MA .
TRENDS IN NEUROSCIENCES, 1999, 22 (09) :391-397