D. Mahe et al., Identification and IFN gamma-regulation of differentially expressed mRNAs in murine microglial and CNS-associated macrophage subpopulations, MOL CELL NE, 18(4), 2001, pp. 363-380
CNS-resident macrophages (microglia and CNS-associated macrophages) are the
main immunocompetent cells of the central nervous system (CNS) and respond
by rapid activation to brain injury. Molecular events occurring during IFN
gamma -activation and identification of potential markers of the CNS-resid
ent macrophage subsets were investigated using microglial-derived clones (E
OC) differing in their morphology and their antigen presenting activities f
or CD4(+) and CD8(+) T-cells. By applying the subtractive process of cDNA r
epresentational difference analysis (cRDA), 16 differentially expressed mRN
As were isolated and sequenced, revealing 8 known and 8 novel molecules; 15
of these messages were unpreviously reported in microglia. Two markers of
all activated microglial EOC cells were identified (iNOS; IRG-1) and specif
ic subpopulation markers were highlighted, including molecules known to be
closely expressed in perivascular spaces. Moreover, some messages could sup
port the distinct morphology, adhesive characteristics, and potential funct
ions of the different clones.