Identification of genes preferentially expressed by microglia and upregulated during cuprizone-induced inflammation

被引:79
作者
Bedard, Andreanne [1 ]
Tremblay, Pierrot [1 ]
Chernomoretz, Ariel [1 ]
Vallieres, Luc [1 ]
机构
[1] Univ Laval Hosp, Res Ctr, Dept Oncol & Mol Endocrinol, Quebec City, PQ G1V 4G2, Canada
关键词
microglia; monocytes; spleen macrophages; DNA microarray; gene profiling; cuprizone; demyelination; G protein-coupled receptor;
D O I
10.1002/glia.20477
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Microglia, monocytes, and peripheral macrophages share a common origin and many characteristics, but what distinguishes them from each other at the level of gene expression remains largely unknown. In this study, we compared the transcriptional profiles of freshly purified microglia, monocytes, and spleen macrophages using Affymetrix Mouse Genome arrays to identify genes predominantly expressed by microglia. Among tens of thousands of genes assayed, 127 potential candidates were found, including nine newly discovered genes encoding plasma membrane and extracellular proteins. In the brain, the latter were selectively expressed by microglia, as revealed by in situ hybridization. Three of them were confirmed to be exclusively (MSR2) or predominantly (GPR12, GPR34) expressed in the brain compared to the other tissues examined. Furthermore, all of these genes were upregulated in activated microglia after treatment with the demyelinating toxin cuprizone, suggesting that they play roles in neuroinflammation. In conclusion, this study reports the identification of new selective markers for microglia, which should prove useful not only to identify and isolate these cells, but also to better understand their distinctive properties. (c) 2007 Wiley-Liss, Inc.
引用
收藏
页码:777 / 789
页数:13
相关论文
共 41 条
[1]   Microarray analysis of activated mixed glial (microglia) and monocyte-derived macrophage gene expression [J].
Albright, AV ;
González-Scarano, F .
JOURNAL OF NEUROIMMUNOLOGY, 2004, 157 (1-2) :27-38
[2]   Immune function of microglia [J].
Aloisi, F .
GLIA, 2001, 36 (02) :165-179
[3]   Unique inflammatory RNA profiles of microglia in Creutzfeldt-Jakob disease [J].
Baker, CA ;
Manuelidis, L .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (02) :675-679
[4]   A distinct and unique transcriptional program expressed by tumor-associated macrophages (defective NF-κB and enhanced IRF-3/STAT1 activation) [J].
Biswas, SK ;
Gangi, L ;
Paul, S ;
Schioppa, T ;
Saccani, A ;
Sironi, M ;
Bottazzi, B ;
Doni, A ;
Vincenzo, B ;
Pasqualini, F ;
Vago, L ;
Nebuloni, M ;
Mantovani, A ;
Sica, A .
BLOOD, 2006, 107 (05) :2112-2122
[5]   Siglec-H is an IPC-specific receptor that modulates type IIFN secretion through DAP12 [J].
Blasius, AL ;
Cella, M ;
Maldonado, J ;
Takai, T ;
Colonna, M .
BLOOD, 2006, 107 (06) :2474-2476
[6]   A role for triggering receptor expressed on myeloid cells-1 in host defense during the early-induced and adaptive phases of the immune response [J].
Bleharski, JR ;
Kiessler, V ;
Buonsanti, C ;
Sieling, PA ;
Stenger, S ;
Colonna, M ;
Modlin, RL .
JOURNAL OF IMMUNOLOGY, 2003, 170 (07) :3812-3818
[7]   Cutting edge: Inflammatory responses can be triggered by TREM-1, a novel receptor expressed on neutrophils and monocytes [J].
Bouchon, A ;
Dietrich, J ;
Colonna, M .
JOURNAL OF IMMUNOLOGY, 2000, 164 (10) :4991-4995
[8]   Impaired differentiation of osteoclasts in TREM-2-deficient individuals [J].
Cella, M ;
Buonsanti, C ;
Strader, C ;
Kondo, T ;
Salmaggi, A ;
Colonna, M .
JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 198 (04) :645-651
[9]   Identification of new CNS-resident macrophage subpopulation molecular markers for the discrimination with murine systemic macrophages [J].
Donnou, S ;
Fisson, S ;
Mahe, D ;
Montoni, A ;
Couez, D .
JOURNAL OF NEUROIMMUNOLOGY, 2005, 169 (1-2) :39-49
[10]   Microglia in culture: What genes do they express? [J].
Duke, DC ;
Moran, LB ;
Turkheimer, FE ;
Banati, R ;
Graeber, MB .
DEVELOPMENTAL NEUROSCIENCE, 2004, 26 (01) :30-37