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10.1038/ni.3306

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suck abstract from ncbi


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pmid26681459
      Nat+Immunol 2016 ; 17 (1 ): 26-33
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  • Molecular control of activation and priming in macrophages #MMPMID26681459
  • Glass CK ; Natoli G
  • Nat Immunol 2016[Jan]; 17 (1 ): 26-33 PMID26681459 show ga
  • In tissues, macrophages are exposed to metabolic, homeostatic and immunoregulatory signals of local or systemic origin that influence their basal functions and responses to danger signals. Signal-transduction pathways regulated by extracellular signals are coupled to distinct sets of broadly expressed stimulus-regulated transcription factors whose ability to elicit gene-expression changes is influenced by the accessibility of their binding sites in the macrophage genome. In turn, accessibility of macrophage-specific transcriptional regulatory elements (enhancers and promoters) is specified by transcription factors that determine the macrophage lineage or impose their tissue-specific properties. Here we review recent findings that advance the understanding of mechanisms underlying priming and signal-dependent activation of macrophages and discuss the effect of genetic variation on these processes.
  • |*Macrophages/cytology/immunology [MESH]
  • |Animals [MESH]
  • |Epigenesis, Genetic/*immunology [MESH]
  • |Gene Expression Regulation/immunology [MESH]
  • |Humans [MESH]
  • |Macrophage Activation/*immunology [MESH]


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