Hematogenous macrophages express CD8 and distribute to regions of lesion cavitation after spinal cord injury

被引:71
作者
Popovich, PG
van Rooijen, N
Hickey, WF
Preidis, G
McGaughy, V
机构
[1] Ohio State Univ, Coll Med & Publ Hlth, Dept Mol Virol Immunol & Med Genet, Columbus, OH 43210 USA
[2] Vrije Univ Amsterdam, Dept Cell Biol & Immunol, NL-1081 BT Amsterdam, Netherlands
[3] DHMC, Dartmouth Med Sch, Dept Pathol, Lebanon, NH 03756 USA
关键词
D O I
10.1016/S0014-4886(03)00120-1
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Historically, CD4 and CD8 antigens have been used to designate functionally distinct T-lymphocyte subsets. However, these antigens also have been described on macrophages in the normal and pathologic central nervous system (CNS). Signaling through CD4 or CD8 may impart unique functions in macrophage subsets that express these antigens. In the current study, the distribution and temporal patterns of expression of CD4 and CD8 were evaluated on various cell types within the traumatically injured spinal cord. The data reveal divergent patterns of CD4 and CD8 expression on unique macrophage populations. Specifically, we show sustained elevations of CD4 expression on microglia and macrophages throughout the lesion site and spared white matter. In contrast, CD8 is predominantly associated with hematogenous macrophages that are recruited from the blood during the first week postinjury. The distribution of CD8-positive cells is restricted to areas of necrotic cavitation. Differential signaling of resident and recruited macrophages through CD4 or CD8 may explain the apparent dichotomy of CNS-macrophage-mediated injury and repair. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:275 / 287
页数:13
相关论文
共 54 条
[1]   ALTERED IMMUNOEXPRESSION OF MICROGLIA AND MACROPHAGES AFTER MILD HEAD-INJURY [J].
AIHARA, N ;
HALL, JJ ;
PITTS, LH ;
FUKUDA, K ;
NOBLE, LJ .
JOURNAL OF NEUROTRAUMA, 1995, 12 (01) :53-63
[2]  
AlberatiGiani D, 1996, J NEUROCHEM, V66, P996
[3]   TNFα promotes proliferation of oligodendrocyte progenitors and remyelination [J].
Arnett, HA ;
Mason, J ;
Marino, M ;
Suzuki, K ;
Matsushima, GK ;
Ting, JPY .
NATURE NEUROSCIENCE, 2001, 4 (11) :1116-1122
[4]   CYTOTOXICITY OF MICROGLIA [J].
BANATI, RB ;
GEHRMANN, J ;
SCHUBERT, P ;
KREUTZBERG, GW .
GLIA, 1993, 7 (01) :111-118
[5]   CXCR4-activated astrocyte glutamate release via TNFa: amplification by microglia triggers neurotoxicity [J].
Bezzi, P ;
Domercq, M ;
Brambilla, L ;
Galli, R ;
Schols, D ;
De Clercq, E ;
Vescovi, A ;
Bagetta, G ;
Kollias, G ;
Meldolesi, J ;
Volterra, A .
NATURE NEUROSCIENCE, 2001, 4 (07) :702-710
[6]   EFFECTS OF SILICA ON THE OUTCOME FROM EXPERIMENTAL SPINAL-INJURY - IMPLICATION OF MACROPHAGES IN SECONDARY TISSUE-DAMAGE [J].
BLIGHT, AR .
NEUROSCIENCE, 1994, 60 (01) :263-273
[7]   QUINOLINIC ACID ACCUMULATION AND FUNCTIONAL DEFICITS FOLLOWING EXPERIMENTAL SPINAL-CORD INJURY [J].
BLIGHT, AR ;
COHEN, TI ;
SAITO, K ;
HEYES, MP .
BRAIN, 1995, 118 :735-752
[8]   Role of IL-1α and IL-1β in ischemic brain damage [J].
Boutin, H ;
LeFeuvre, RA ;
Horai, R ;
Asano, M ;
Iwakura, Y ;
Rothwell, NJ .
JOURNAL OF NEUROSCIENCE, 2001, 21 (15) :5528-5534
[9]   Novel role of human CD4 molecule identified in neurodegeneration [J].
Buttini, M ;
Westland, CE ;
Masliah, E ;
Yafeh, AM ;
Wyss-Coray, T ;
Mucke, L .
NATURE MEDICINE, 1998, 4 (04) :441-446
[10]   SPECIES HETEROGENEITY IN MACROPHAGE EXPRESSION OF THE CD4 ANTIGEN [J].
CROCKER, PR ;
JEFFERIES, WA ;
CLARK, SJ ;
CHUNG, LP ;
GORDON, S .
JOURNAL OF EXPERIMENTAL MEDICINE, 1987, 166 (02) :613-618