Granulocyte-Macrophage Colony-Stimulating Factor Induces an Expression Program in Neonatal Microglia That Primes Them for Antigen Presentation
Author(s) -
Fabio Re,
Svetlana Belyanskaya,
Richiard J. Riese,
Barbara Cipriani,
Falko R. Fischer,
Francesca Granucci,
Paola RicciardiCastagnoli,
Celia F. Brosnan,
Lawrence J. Stern,
Jack L. Strominger,
Laura Santambrogio
Publication year - 2002
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.169.5.2264
Subject(s) - microglia , antigen presentation , granulocyte macrophage colony stimulating factor , biology , priming (agriculture) , reprogramming , immunology , macrophage , function (biology) , colony stimulating factor , gene expression , innate immune system , microbiology and biotechnology , phenotype , immune system , gene , t cell , cytokine , in vitro , inflammation , haematopoiesis , genetics , stem cell , botany , germination
Neonatal microglial cells respond to GM-CSF and M-CSF by acquiring different morphologies and phenotypes. To investigate the extent and consequences of this process, a global gene expression analysis was performed, with significant changes in transcript levels confirmed by biochemical analyses. Primary murine microglial cells underwent substantial expression reprogramming after treatment with GM-CSF or M-CSF with many differentially expressed transcripts important in innate and adaptive immunity. In particular, many gene products involved in Ag presentation were induced by GM-CSF, but not M-CSF, thus potentially priming relatively quiescent microglia cells for Ag presentation. This function of GM-CSF is distinct from its primary function in cell proliferation and survival.
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