TY - JOUR
T1 - A nuclear receptor atlas
T2 - Macrophage activation
AU - Barish, Grant D.
AU - Downes, Michael
AU - Alaynick, William A.
AU - Yu, Ruth T.
AU - Ocampo, Corinne B.
AU - Bookout, Angie L.
AU - Mangelsdorf, David J.
AU - Evans, Ronald M.
PY - 2005/10
Y1 - 2005/10
N2 - Macrophage activation is an essential cellular process underlying innate immunity, enabling the body to combat bacteria and other pathogens. In addition to host defense, activated macrophages play a central role in atherogenesis, autoimmunity, and a variety of inflammatory diseases. As members of the Nuclear Receptor Signaling Atlas (NURSA) program, we employed quantitative real-time PCR (qPCR) to provide a comprehensive assessment of changes in expression of the 49 members of the murine nuclear receptor superfamily. In this study, we have identified a network of 28 nuclear receptors associated with the activation of bone marrow-derived macrophages by lipopolysaccharide or the prototypic cytokine interferon γ. More than half of this network is deployed in three intricate and highly scripted temporal phases that are unique for each activator. Thus, early receptors whose expression peaks within 4 h after lipopolysaccharide exposure, such as glucocorticoid receptor, peroxisome proliferator-activated receptor γ, and neuronal growth factor 1B, are found as late rising markers of the interferon γ cascade, occurring 16 h or later. The discovery of precise serial expression patterns reveals that macrophage activation is the product of an underlying process that impacts the genome within minutes and identifies a collection of new therapeutic targets for controlling inflammation by disruption of presumptive regulatory cascades.
AB - Macrophage activation is an essential cellular process underlying innate immunity, enabling the body to combat bacteria and other pathogens. In addition to host defense, activated macrophages play a central role in atherogenesis, autoimmunity, and a variety of inflammatory diseases. As members of the Nuclear Receptor Signaling Atlas (NURSA) program, we employed quantitative real-time PCR (qPCR) to provide a comprehensive assessment of changes in expression of the 49 members of the murine nuclear receptor superfamily. In this study, we have identified a network of 28 nuclear receptors associated with the activation of bone marrow-derived macrophages by lipopolysaccharide or the prototypic cytokine interferon γ. More than half of this network is deployed in three intricate and highly scripted temporal phases that are unique for each activator. Thus, early receptors whose expression peaks within 4 h after lipopolysaccharide exposure, such as glucocorticoid receptor, peroxisome proliferator-activated receptor γ, and neuronal growth factor 1B, are found as late rising markers of the interferon γ cascade, occurring 16 h or later. The discovery of precise serial expression patterns reveals that macrophage activation is the product of an underlying process that impacts the genome within minutes and identifies a collection of new therapeutic targets for controlling inflammation by disruption of presumptive regulatory cascades.
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U2 - 10.1210/me.2004-0529
DO - 10.1210/me.2004-0529
M3 - Article
C2 - 16051664
AN - SCOPUS:25444448223
SN - 0888-8809
VL - 19
SP - 2466
EP - 2477
JO - Molecular Endocrinology
JF - Molecular Endocrinology
IS - 10
ER -