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Background <p>Gut-liver crosstalk exacerbates hepatic injury in gut ischemia/reperfusion (I/R), but its mechanism and therapeutic intervention remain elusive. Given the important roles of neutrophils and gut-resident intraepithelial lymphocytes (IELs) during acute inflammation, we hypothesized that the interaction between these two cell types worsens liver injury during gut I/R.</p> Methods <p>Gut I/R was induced in mice by occluding superior mesenteric artery (SMA) for 60&#xa0;min, followed by 4&#xa0;h resuscitation. Blood, intestine and liver tissues were collected for various analysis. Neutrophil extracellular traps (NETs) were determined by microscopy. Gut I/R mice were injected (i.p.) with DPX2 (1&#xa0;µg/g BW) at the time of reperfusion. After 4&#xa0;h, blood and liver tissues were collected for various analysis.</p> Results <p>We discovered that neutrophils in contact with IELs in gut I/R mice had increased ability to form NETs. As such, NETs<sup>+</sup> neutrophils were increased in the portal vein blood of gut I/R mice compared to sham mice and the systemic blood, accompanied by increased NETs in the liver, indicating the migration of the activated neutrophils from the gut to the liver. Adoptive transfer of IEL-primed neutrophils into gut I/R mice exacerbated liver inflammation as indicated by increased liver tissue levels of inducible nitric oxide synthase (iNOS), interleukin-6 (IL-6), interleukin-1 beta (IL-1β), keratinocyte-derived chemokine (KC), and C-X-C motif chemokine ligand 2 (CXCL2). The interaction of neutrophils and IELs is known to be mediated via neutrophil CD112. Increased numbers of CD112<sup>+</sup> neutrophils were observed in the gut epithelium after gut I/R. We have discovered a CD112-derived peptide, named DPX2, which inhibits the interaction between CD112 on neutrophils and its proinflammatory ligand CD226 on IELs. In vitro, DPX2 attenuated IEL-induced NETosis under inflammatory conditions. In vivo, the administration of DPX2 significantly decreased NET-forming neutrophils in the portal vein of gut I/R mice. In parallel to NETs inhibition, DPX2 administration significantly mitigated the gene expression of iNOS, IL-6, IL-1β, KC, and CXCL2 in the liver. Furthermore, the administration of DPX2 significantly attenuated liver injury as indicated by decreased serum aspartate aminotransferase (AST) and alanine aminotransferase (ALT), tissue injury score, and liver cell death.</p> Conclusions <p>Neutrophil-gut IEL interaction mediates proinflammatory gut-liver crosstalk and the novel CD112-derived peptide DPX2 targeting this interaction has the potential to mitigate hepatic injury.</p>

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A novel CD112-derived peptide targeting gut-primed neutrophils to attenuate deadly hepatic injury

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2026年2月17日

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  • Takayuki Kato,
  • Atsushi Murao,
  • Alok Jha,
  • Gaifeng Ma,
  • Monowar Aziz,
  • Ping Wang

摘要

Background

Gut-liver crosstalk exacerbates hepatic injury in gut ischemia/reperfusion (I/R), but its mechanism and therapeutic intervention remain elusive. Given the important roles of neutrophils and gut-resident intraepithelial lymphocytes (IELs) during acute inflammation, we hypothesized that the interaction between these two cell types worsens liver injury during gut I/R.

Methods

Gut I/R was induced in mice by occluding superior mesenteric artery (SMA) for 60 min, followed by 4 h resuscitation. Blood, intestine and liver tissues were collected for various analysis. Neutrophil extracellular traps (NETs) were determined by microscopy. Gut I/R mice were injected (i.p.) with DPX2 (1 µg/g BW) at the time of reperfusion. After 4 h, blood and liver tissues were collected for various analysis.

Results

We discovered that neutrophils in contact with IELs in gut I/R mice had increased ability to form NETs. As such, NETs+ neutrophils were increased in the portal vein blood of gut I/R mice compared to sham mice and the systemic blood, accompanied by increased NETs in the liver, indicating the migration of the activated neutrophils from the gut to the liver. Adoptive transfer of IEL-primed neutrophils into gut I/R mice exacerbated liver inflammation as indicated by increased liver tissue levels of inducible nitric oxide synthase (iNOS), interleukin-6 (IL-6), interleukin-1 beta (IL-1β), keratinocyte-derived chemokine (KC), and C-X-C motif chemokine ligand 2 (CXCL2). The interaction of neutrophils and IELs is known to be mediated via neutrophil CD112. Increased numbers of CD112+ neutrophils were observed in the gut epithelium after gut I/R. We have discovered a CD112-derived peptide, named DPX2, which inhibits the interaction between CD112 on neutrophils and its proinflammatory ligand CD226 on IELs. In vitro, DPX2 attenuated IEL-induced NETosis under inflammatory conditions. In vivo, the administration of DPX2 significantly decreased NET-forming neutrophils in the portal vein of gut I/R mice. In parallel to NETs inhibition, DPX2 administration significantly mitigated the gene expression of iNOS, IL-6, IL-1β, KC, and CXCL2 in the liver. Furthermore, the administration of DPX2 significantly attenuated liver injury as indicated by decreased serum aspartate aminotransferase (AST) and alanine aminotransferase (ALT), tissue injury score, and liver cell death.

Conclusions

Neutrophil-gut IEL interaction mediates proinflammatory gut-liver crosstalk and the novel CD112-derived peptide DPX2 targeting this interaction has the potential to mitigate hepatic injury.