A nuclear receptor atlas: Macrophage activation

Grant D. Barish, Michael Downes, William A. Alaynick, Ruth T. Yu, Corinne B. Ocampo, Angie L. Bookout, David J. Mangelsdorf, Ronald M. Evans

Research output: Contribution to journalArticlepeer-review

118 Scopus citations


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.

Original languageEnglish (US)
Pages (from-to)2466-2477
Number of pages12
JournalMolecular Endocrinology
Issue number10
StatePublished - Oct 2005

ASJC Scopus subject areas

  • Molecular Biology
  • Endocrinology


Dive into the research topics of 'A nuclear receptor atlas: Macrophage activation'. Together they form a unique fingerprint.

Cite this