Biology, role and therapeutic potential of circulating histones in acute inflammatory disorders

J Cell Mol Med. 2018 Oct;22(10):4617-4629. doi: 10.1111/jcmm.13797. Epub 2018 Aug 7.

Abstract

Histones are positively charged nuclear proteins that facilitate packaging of DNA into nucleosomes common to all eukaryotic cells. Upon cell injury or cell signalling processes, histones are released passively through cell necrosis or actively from immune cells as part of extracellular traps. Extracellular histones function as microbicidal proteins and are pro-thrombotic, limiting spread of infection or isolating areas of injury to allow for immune cell infiltration, clearance of infection and initiation of tissue regeneration and repair. Histone toxicity, however, is not specific to microbes and contributes to tissue and end-organ injury, which in cases of systemic inflammation may lead to organ failure and death. This review details the processes of histones release in acute inflammation, the mechanisms of histone-related tissue toxicity and current and future strategies for therapy targeting histones in acute inflammatory diseases.

Keywords: extracellular histones; immunothrombosis; inflammation; innate immunity.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Alarmins / blood
  • Alarmins / genetics
  • Alarmins / immunology*
  • Anti-Inflammatory Agents / therapeutic use
  • Blood Coagulation Factors / genetics
  • Blood Coagulation Factors / immunology
  • Chemotactic Factors / blood
  • Chemotactic Factors / genetics
  • Chemotactic Factors / immunology
  • Chemotaxis / immunology
  • Communicable Diseases / genetics
  • Communicable Diseases / immunology*
  • Communicable Diseases / pathology
  • Communicable Diseases / therapy
  • Extracellular Space / chemistry
  • Extracellular Space / immunology
  • Extracellular Traps / chemistry
  • Extracellular Traps / immunology
  • Gene Expression Regulation
  • Histones / blood
  • Histones / genetics
  • Histones / immunology*
  • Humans
  • Immunity, Innate
  • Inflammation
  • Necrosis / genetics
  • Necrosis / immunology*
  • Necrosis / pathology
  • Necrosis / therapy
  • Neutrophils
  • Receptors, Pattern Recognition / genetics
  • Receptors, Pattern Recognition / immunology*
  • Signal Transduction
  • Thrombosis / genetics
  • Thrombosis / immunology*
  • Thrombosis / pathology
  • Thrombosis / therapy

Substances

  • Alarmins
  • Anti-Inflammatory Agents
  • Blood Coagulation Factors
  • Chemotactic Factors
  • Histones
  • Receptors, Pattern Recognition