Expression patterns of group III metabotropic glutamate receptors mGluR4 and mGluR8 in multiple sclerosis lesions

被引:56
作者
Geurts, JJG
Wolswijk, G
Bö, L
Redeker, S
Ramkema, M
Troost, D
Aronica, E
机构
[1] Univ Amsterdam, Acad Med Ctr, Dept Neuropathol, NL-1105 AZ Amsterdam, Netherlands
[2] Vrije Univ Amsterdam Med Ctr, MS Res Ctr, Amsterdam, Netherlands
[3] Vrije Univ Amsterdam Med Ctr, Dept Radiol, Amsterdam, Netherlands
[4] Netherlands Inst Brain Res, Amsterdam, Netherlands
[5] Vrije Univ Amsterdam Med Ctr, Dept Pathol, Amsterdam, Netherlands
关键词
metabotropic glutamate receptors; multiple sclerosis; microglia; macrophages; reactive astrocytes;
D O I
10.1016/j.jneuroim.2004.08.012
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Recent evidence supports a role for metabotropic glutamate receptors (mGluRs) in neuroinflammatory diseases. In the present study, we have investigated whether the group III mGluR subtypes mGluR4 and mGluR8 are expressed in MS lesions at various stages of evolution. In control patient tissue and in normal-appearing MS white matter (NAWM), no microglial or astrocyte staining was detected. In contrast, in active lesions, mGluR8 immunoreactivity (IR) was detected in cells of the microglia/macrophage lineage. Fewer macrophage-like cells were positive for mGluR8 in chronic active and inactive lesions. No mGluR4 IR was detected in cells of the microglia/macrophage lineage in the MS lesions studied. In chronic active lesions, however, a population of reactive astrocytes localized in the rim of the lesions expressed both mGluR4 and mGluR8. Our results suggest a role for these receptor subtypes in the inflammatory response in MS that involves both astrocytes and cells of the microglia/macrophage lineage. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:182 / 190
页数:9
相关论文
共 60 条
[31]   Glutamate receptor-mediated toxicity in optic nerve oligodendrocytes [J].
Matute, C ;
SanchezGomez, MV ;
MartinezMillan, L ;
Miledi, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (16) :8830-8835
[32]  
Matute C, 1999, ADV EXP MED BIOL, V468, P97
[33]   Glutamate on demand: Astrocytes as a ready source [J].
Mazzanti, M ;
Sul, JY ;
Haydon, PG .
NEUROSCIENTIST, 2001, 7 (05) :396-405
[34]   Oligodendrocytes from forebrain are highly vulnerable to AMPA/kainate receptor-mediated excitotoxicity [J].
McDonald, JW ;
Althomsons, SP ;
Hyrc, KL ;
Choi, DW ;
Goldberg, MP .
NATURE MEDICINE, 1998, 4 (03) :291-297
[35]   Concepts of viral pathogenesis of multiple sclerosis [J].
Meinl, E .
CURRENT OPINION IN NEUROLOGY, 1999, 12 (03) :303-307
[36]   ROLES OF METABOTROPIC GLUTAMATE RECEPTORS IN BRAIN PLASTICITY AND PATHOLOGY [J].
MILLER, S ;
KESSLAK, JP ;
ROMANO, C ;
COTMAN, CW .
DIVERSITY OF INTERACTING RECEPTORS, 1995, 757 :460-474
[37]   Structural organization of the mouse metabotropic glutamate receptor subtype 3 gene and its regulation by growth factors in cultured cortical astrocytes [J].
Minoshima, T ;
Nakanishi, S .
JOURNAL OF BIOCHEMISTRY, 1999, 126 (05) :889-896
[38]   Glutamate receptors: brain function and signal transduction [J].
Nakanishi, S ;
Nakajima, Y ;
Masu, M ;
Ueda, Y ;
Nakahara, K ;
Watanabe, D ;
Yamaguchi, S ;
Kawabata, S ;
Okada, M .
BRAIN RESEARCH REVIEWS, 1998, 26 (2-3) :230-235
[39]   Medical progress: Multiple sclerosis. [J].
Noseworthy, JH ;
Lucchinetti, C ;
Rodriguez, M ;
Weinshenker, BG .
NEW ENGLAND JOURNAL OF MEDICINE, 2000, 343 (13) :938-952
[40]   Progress in determining the causes and treatment of multiple sclerosis [J].
Noseworthy, JH .
NATURE, 1999, 399 (6738) :A40-A47