Enhanced expression of chemotactic receptors in multiple sclerosis lesions

被引:78
作者
MullerLadner, U
Jones, JL
Wetsel, RA
Gay, S
Raine, CS
Barnum, SR
机构
[1] UNIV ALABAMA, DEPT MED, DIV CLIN IMMUNOL & RHEUMATOL, BIRMINGHAM, AL 35294 USA
[2] UNIV ALABAMA, DEPT MICROBIOL, BIRMINGHAM, AL 35294 USA
[3] WASHINGTON UNIV, SCH MED, DEPT PEDIAT, ST LOUIS, MO 63110 USA
[4] WASHINGTON UNIV, SCH MED, DEPT MOL MICROBIOL, ST LOUIS, MO 63110 USA
[5] YESHIVA UNIV ALBERT EINSTEIN COLL MED, DEPT PATHOL NEUROPATHOL, BRONX, NY 10461 USA
[6] YESHIVA UNIV ALBERT EINSTEIN COLL MED, DEPT NEUROL & NEUROSCI, BRONX, NY 10461 USA
关键词
receptor; multiple sclerosis; complement; chemokine; astrocyte; microglia;
D O I
10.1016/S0022-510X(96)00217-1
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We have previously shown that astrocytes and microglia express the receptors for C5a, interleukin-8 (IL-8) and N-formyl-Met-Leu-Phe (FMLP) in vitro. The expression and function of chemotactic receptors in the central nervous system (CNS) is, however, largely unexplored. In this study, we examined tissue sections from normal human brain and active, chronic active and chronic silent multiple sclerosis (MS) lesions for the expression of the receptors for C5a, IL-8 and FMLP by immunohistochemistry. In normal brain tissue, the expression of all three receptors was seen at low levels on astrocytes and microglia. In contrast, expression for all three receptors was markedly elevated on foamy macrophages in the acute and chronic active MS lesions. In addition, fibrous astrocytes stained intensely for the C5a receptor in the chronic active disease. Receptor expression in the chronic silent lesion was low and similar to that seen in normal brain, with staining confined to a few hypertrophic astrocytes and foamy macrophages. These are the first studies to demonstrate expression of these receptors in the CNS and elevated receptor expression in inflammatory MS lesions. The data suggest that these chemotactic receptors may play a role in inflammatory responses in MS and possibly in other CNS diseases.
引用
收藏
页码:135 / 141
页数:7
相关论文
共 43 条
[1]   TYPE-1 ASTROCYTES AND OLIGODENDROCYTE-TYPE-2 ASTROCYTE GLIAL PROGENITORS MIGRATE TOWARD DISTINCT MOLECULES [J].
ARMSTRONG, RC ;
HARVATH, L ;
DUBOISDALCQ, ME .
JOURNAL OF NEUROSCIENCE RESEARCH, 1990, 27 (03) :400-407
[2]   THE CHEMOATTRACTANT DES-ARG74-C5A REGULATES THE EXPRESSION OF ITS OWN RECEPTOR ON A MONOCYTE-LIKE CELL-LINE [J].
BARKER, MD ;
JOSE, PJ ;
WILLIAMS, TJ ;
BURTON, DR .
BIOCHEMICAL JOURNAL, 1986, 236 (02) :621-624
[3]  
BRANDES ME, 1991, J IMMUNOL, V147, P1600
[4]   CYTOKINE LOCALIZATION IN MULTIPLE-SCLEROSIS LESIONS - CORRELATION WITH ADHESION MOLECULE EXPRESSION AND REACTIVE NITROGEN SPECIES [J].
BROSNAN, CF ;
CANNELLA, B ;
BATTISTINI, L ;
RAINE, CS .
NEUROLOGY, 1995, 45 (06) :S16-S21
[5]  
BURG M, 1995, J IMMUNOL, V155, P4419
[6]   THE ADHESION MOLECULE AND CYTOKINE PROFILE OF MULTIPLE-SCLEROSIS LESIONS [J].
CANNELLA, B ;
RAINE, CS .
ANNALS OF NEUROLOGY, 1995, 37 (04) :424-435
[7]  
CARLOS TM, 1994, BLOOD, V84, P2068
[8]   MITOCHONDRIAL N-FORMYLMETHIONYL PROTEINS AS CHEMOATTRACTANTS FOR NEUTROPHILS [J].
CARP, H .
JOURNAL OF EXPERIMENTAL MEDICINE, 1982, 155 (01) :264-275
[9]  
COLLINS SJ, 1987, BLOOD, V70, P1233
[10]  
CROSS AH, 1992, SEMIN NEUROSCI, V4, P213