Abnormal neutrophil traps and impaired efferocytosis contribute to liver injury and sepsis severity after binge alcohol use
Author(s): ,
Gyongyi Szabo
Affiliations:
Department of Medicine, University of Massachusetts Medical School, Worcester, MA 01605, USA
Corresponding author. Address: Department of Medicine, University of Massachusetts Medical School LRB208, 364 Plantation Street, Worcester, MA 01605, USA. Tel.: +1-508-856-5275; fax: +1-508-856-4770.
,
Karen Kodys
Affiliations:
Department of Medicine, University of Massachusetts Medical School, Worcester, MA 01605, USA
,
Donna Catalano
Affiliations:
Department of Medicine, University of Massachusetts Medical School, Worcester, MA 01605, USA
,
Benedek Gyongyosi
Affiliations:
Department of Medicine, University of Massachusetts Medical School, Worcester, MA 01605, USA
,
Aditya Ambade
Affiliations:
Department of Medicine, University of Massachusetts Medical School, Worcester, MA 01605, USA
,
Istvan Furi
Affiliations:
Department of Medicine, University of Massachusetts Medical School, Worcester, MA 01605, USA
,
Adeyinka Adejumo
Affiliations:
Department of Medicine, University of Massachusetts Medical School, Worcester, MA 01605, USA
,
Patrick Lowe
Affiliations:
Department of Medicine, University of Massachusetts Medical School, Worcester, MA 01605, USA
,
Banishree Saha
Affiliations:
Department of Medicine, University of Massachusetts Medical School, Worcester, MA 01605, USA
,
Arvin Iracheta-Vellve
Affiliations:
Department of Medicine, University of Massachusetts Medical School, Worcester, MA 01605, USA
,
Yeonhee Cho
Affiliations:
Department of Medicine, University of Massachusetts Medical School, Worcester, MA 01605, USA
Terence Ndonyi Bukong
Affiliations:
INRS-Institut Armand-Frappier, Institut National de la Recherche Scientifique, Laval, Québec, Canada
EASL LiverTree™. Szabo G. Nov 1, 2018; 256712
Dr. Gyongyi Szabo
Dr. Gyongyi Szabo

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Graphical abstract

Graphical abstract

Alcohol treatment induces spontaneous neutrophil extracellular trap (NET) formation. Alcohol impairs further NET release by the same neutrophils upon subsequent activation. Alcohol reduces efferocytosis by macrophages, leading to less clearance of NETotic neutrophils. Depletion of neutrophils in vivo alleviates hepatic injury after binge-drinking.

Background & Aims

Neutrophil extracellular traps (NETs) are an important strategy utilized by neutrophils to immobilize and kill invading microorganisms. Herein, we studied NET formation and the process of neutrophil cell death (NETosis), as well as the clearance of NETs by macrophages (MΦ) (efferocytosis) in acute sepsis following binge drinking.

Methods

Healthy volunteers consumed 2 ml of vodka/kg body weight, before blood endotoxin and 16 s rDNA were measured. Peripheral neutrophils were isolated and exposed to alcohol followed by phorbol 12-myristate 13-acetate (PMA) stimulation. Mice were treated with three alcohol binges and intraperitoneal lipopolysaccharide (LPS) to assess the dynamics of NET formation and efferocytosis. In vivo, anti-Ly6G antibody (IA8) was used for neutrophil depletion.

Results

Inducers of NETs (endotoxin and bacterial DNA) significantly increased in the circulation after binge alcohol drinking in humans. Ex vivo, alcohol alone increased NET formation, but upon PMA stimulation alcohol attenuated NET formation. Binge alcohol in mice resulted in a biphasic response to LPS. Initially, binge alcohol reduced LPS-induced NET formation and resulted in a diffuse distribution of neutrophils in the liver compared to alcohol-naïve mice. Moreover, indicators of NET formation including citrullinated histone H3, neutrophil elastase, and neutrophil myeloperoxidase were decreased at an early time point after LPS challenge in mice receiving binge alcohol, suggesting decreased NET formation. However, in the efferocytosis phase (15 h after LPS) citrullinated histone-H3 was increased in the liver in alcohol binge mice, suggesting decreased clearance of NETs. In vitro alcohol treatment reduced efferocytosis and phagocytosis of NETotic neutrophils and promoted expression of CD206 on MΦ. Finally, depletion of neutrophils prior to binge alcohol ameliorated LPS-induced systemic inflammation and liver injury in mice.

Conclusions

Dysfunctional NETosis and efferocytosis following binge drinking exacerbate liver injury associated with sepsis.

Lay summary

Disease severity in alcoholic liver disease (ALD) is associated with a significant presence of neutrophils (a type of immune cell) in the liver. It remains unknown how alcohol affects the capacity of neutrophils to control infection, a major hallmark of ALD. We found that binge alcohol drinking impaired important strategies used by neutrophils to contain and resolve infection, resulting in increased liver injury during ALD.

Keyword(s)
Sepsis, Binge drinking, Alcoholic hepatitis, Neutrophil elastase, Neutrophil depletion
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