Rapid isolation of highly enriched and quiescent microglia from adult rat hippocampus: Immunophenotypic and functional characteristics

被引:137
作者
Frank, MG
Wieseler-Frank, JL
Watkins, LR
Maier, SF
机构
[1] Univ Colorado, Dept Psychol, Boulder, CO 80309 USA
[2] Univ Colorado, Ctr Neurosci, Boulder, CO 80309 USA
关键词
microglia; isolation; density gradient; Percoll; immunophenotype; in situ; CD11b; MHC II;
D O I
10.1016/j.jneumeth.2005.06.026
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Isolation of microglia from CNS tissue provides a powerful too] to study basic microglia biology and examine the effects of in vivo treatments on microglia immunophenotype and function. Previous microglia isolation methodologies utilized whole brain. However, microglia immunophenotype varies across CNS anatomical loci, thus isolation of microglia from whole brain may obscure regional brain variations in microglia immunophenotype and function. In addition, it is unknown to what extent microglia isolation procedures alter the ill situ immunophenotype and function of microglia. The present report details a procedure for the rapid isolation of microglia from discrete CNS anatomical loci and addresses the issue of whether the in situ microglia immunophenotype is significantly altered by the isolation procedure. The present microglia isolation method yielded highly enriched hippocampal microglia, which were devoid of other CNS macrophage subtypes and exhibited attributes reflecting a quiescent phenotype characteristic of microglia observed in situ under non-pathological conditions. Further, isolated microglia exhibited functional responsiveness to immunogenic stimuli ex vivo. The immunophenotypic and functional attributes of isolated microglia suggest that the isolation procedure preserves the in vivo phenotype of microglia, thus providing an experimental method with minimal procedural confounds for examining in vivo treatments on microglia ex vivo. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:121 / 130
页数:10
相关论文
共 20 条
[1]   Gapped BLAST and PSI-BLAST: a new generation of protein database search programs [J].
Altschul, SF ;
Madden, TL ;
Schaffer, AA ;
Zhang, JH ;
Zhang, Z ;
Miller, W ;
Lipman, DJ .
NUCLEIC ACIDS RESEARCH, 1997, 25 (17) :3389-3402
[2]   CNS microvascular pericytes express macrophage-like function, cell surface integrin alpha M, and macrophage marker ED-2 [J].
Balabanov, R ;
Washington, R ;
Wagnerova, J ;
DoreDuffy, P .
MICROVASCULAR RESEARCH, 1996, 52 (02) :127-142
[3]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[4]   Tissue digestion with dispase substantially reduces lymphocyte and macrophage cell-surface antigen expression [J].
Ford, AL ;
Foulcher, E ;
Goodsall, AL ;
Sedgwick, JD .
JOURNAL OF IMMUNOLOGICAL METHODS, 1996, 194 (01) :71-75
[5]  
FORD AL, 1995, J IMMUNOL, V154, P4309
[6]   IDENTITY OF ED2-POSITIVE PERIVASCULAR CELLS IN RAT-BRAIN [J].
GRAEBER, MB ;
STREIT, WJ ;
KREUTZBERG, GW .
JOURNAL OF NEUROSCIENCE RESEARCH, 1989, 22 (01) :103-106
[7]   Microglia, macrophages, perivascular macrophages, and pericytes: a review of function and identification [J].
Guillemin, GJ ;
Brew, BJ .
JOURNAL OF LEUKOCYTE BIOLOGY, 2004, 75 (03) :388-397
[8]  
Havenith CEG, 1998, GLIA, V22, P348, DOI 10.1002/(SICI)1098-1136(199804)22:4<348::AID-GLIA4>3.3.CO
[9]  
2-X
[10]   Microglia: A sensor for pathological events in the CNS [J].
Kreutzberg, GW .
TRENDS IN NEUROSCIENCES, 1996, 19 (08) :312-318