Lung inflammation and damage induced by extracellular histones

Despite decades of research, acute respiratory distress syndrome (ARDS) remains an important clinical challenge due to an incomplete understanding of the pathophysiological mechanisms. No FDA-approved drug therapy currently exists for treatment of humans with ARDS. There is accumulating evidence in rodents and humans suggesting that extracellular histones are strong drivers of inflammation and tissue damage. We recently described an important role for extracellular histones during acute lung injury (ALI) in mice (Bosmann et al., FASEB J. 27:50105021 (2013)). Extracellular histones were detected in bronchoalveolar lavage fluids (BALF) from patients with ARDS but not in BALF from non-ARDS patients in intensive care units. Extracellular histones were also detected in BALF from mice during experimental ALI. The presence of extracellular histones was dependent on the two C5a receptors (C5aR and C5L2) and availability of neutrophils. Extracellular histones were highly pro-inflammatory, and caused severe damage to respiratory function. Intratracheal instillation of histones resulted in pro-inflammatory mediator production, epithelial cell damage, disturbances in alveolar-capillary gas exchange, lung consolidation, activation of the coagulation cascade, and in some cases, death. Antibody-mediated neutralization of extracellular histones attenuated C5a-induced ALI. Together, these data suggested a prominent role for extracellular histones in the pathophysiology of ALI. The predominant source of histones in ALI may be neutrophils that have been activated by C5a to form neutrophil extracellular traps (NETs). Therapeutic targeting of extracellular histones may provide a novel approach to combat ARDS in humans.

Copyright: © 2014 The Authors.Licensed under a Creative Commons Attribution 4.0 International License which allows users including authors of articles to copy and redistribute the material in any medium or format, in addition to remix, transform, and build upon the material for any purpose, even commercially, as long as the author and original source are properly cited or credited.
Acute respiratory distress syndrome (ARDS) remain significant clinical problems involving >200,000 cases in the United States annually, with mortality rates from 25-60% [1,2] .Acute lung injury (ALI) and ARDS are characterized by the production of pro-inflammatory mediators such as cytokines and chemokines, and

RESEARCH HIGHLIGHT
complement activation products, and the accumulation of neutrophils in the lung.Disruption of the epithelial/endothelial barrier, along with reduced ability to clear alveolar fluid, results in persistent pulmonary edema and lung consolidation, intrapulmonary hemorrhage, and severely impaired gas exchange (reviewed, [3] ).However, the molecular mechanisms of ALI/ARDS pathology remain unclear, and there is no specific FDA-approved drug therapy to improve clinical outcomes.
Evidence has accumulated suggesting that extracellular histones contribute to the pathogenesis of inflammatory diseases.Plasma levels of extracellular histones are elevated during trauma and/or sepsis in humans, baboons, and mice [4][5][6] .Antibody-mediated neutralization of histones provides protection during experimental sepsis in mice and baboons [4] .In our recent report, "Extracellular histones are essential effectors of C5aR-and C5L2-mediated tissue damage and inflammation in acute lung injury" [7] , we investigated the role of extracellular histones during ALI.

Presence of extracellular histones during ARDS/ALI in humans and mice
We detected the presence of extracellular histones in bronchoalveolar lavage fluid (BALF) samples from humans with ARDS.The presence of histones in BALF appeared to peak early (up to 10 days after initial diagnosis of ARDS), and reduced levels were observed at later time points.No extracellular histones were observed in BALF samples from non-ARDS intensive care patients.In mice, extracellular histone levels were elevated in BALF from three different models of ALI (LPS, IgG immune complex, and C5a-induced).Extracellular histone presence was dependent on an intact neutrophil population as well as the two C5a receptors (C5aR and C5L2).Even though neutrophils were required for full histone release during ALI, the exact cellular source of the extracellular histones was not clear.Histones are known to be released by neutrophils associated with neutrophil extracellular traps (NETs), and NETs have been shown to be present during ALI [8] .Conversely, neutrophils may contribute to lung tissue damage and parenchymal cell death, and histones are also known to be released from apoptotic/necrotic cells [9] .

Extracellular histone-induced tissue damage and ALI
The treatment of alveolar type II epithelial cell lines in vitro with purified histones induced elevations of intracellular calcium and cell death.When exogenous histones (20 μg/g body weight) were administered to mice i.t., BALF levels of lactate dehydrogenase (LDH) were elevated after 1 hour indicating extensive tissue damage in lung.Histologic and electron microscopic analysis revealed classical signs of ALI including intra-alveolar hemorrhage, fibrin deposits, and epithelial cell injury after i.t.histone instillation.Exogenous histone instillation into rats (i.t., 50 μg/g body weight) resulted in very rapid disturbances in lung air-gas exchange, cyanosis, and occasional death.Whole-body plethysmography revealed increased respiratory rate, while analysis of blood showed arterial acidification, elevated pCO2, and reduced oxyhemoglobin saturation as early as 15 minutes after histone instillation.Together, these data indicate that extracellular histones resulted in lung tissue damage, and severe and immediate ALI.

Role of extracellular histones in ALI
Figure 1 outlines our current thoughts about the role of extracellular histones during ALI.Histone presence was dependent on both C5a receptors, indicating a significant role for complement activation.Histone presence was also dependent on neutrophils, either through the release of histones associated with NETs, or through neutrophilmediated cell damage and death.Once present, extracellular histones were highly inflammatory and damaging in the lung, and led to intense ALI.

Future directions
Targeting of histone-mediated inflammation and cell damage may be a promising avenue for the development of novel therapeutics for the treatment of ARDS.We have shown that 1) extracellular histones are important for tissue damage and inflammation during rodent ALI; and 2) extracellular histones are present during human ARDS.However, several important questions remain.More investigation is needed to determine the relative contributions of individual histones (H1, H2A, H2B, H3, and H4) during ARDS.In addition, whether all of the individual histones are present in the extracellular space during human ARDS is not known.These are active areas of investigation in our group.Clarification of these important questions is required prior to the development of histone-targeted therapeutics.

Figure 1 .
Figure 1.Role of extracellular histones during ALI.Extracellular histone presence during ALI was dependent on C5a receptors and neutrophils.Extracellular histones are known to be released by activated neutrophils (left pathway) or by dead/dying cells (right pathway).Once formed, extracellular histones lead to inflammation and tissue damage, resulting in ALI.