Enolase‐1 Is a Key Regulator of Neutrophil Recruitment During Acute Inflammation

Enolase-1 (ENO1) is a moonlighting protein with multiple functions. When expressed on the cell surface, ENO1 binds plasminogen (PLG) and promotes cell migration by facilitating plasmin (PLM)-mediated extracellular matrix degradation. Here, we observed that inflammatory stimulation significantly upregulated ENO1 expression on the neutrophil surface, both in vitro and in vivo. An anti-ENO1 monoclonal antibody (mAb), 7E5, which blocks the ENO1-PLG interaction, effectively suppressed neutrophil invasion in vitro. In mouse models of acute inflammation, including lipopolysaccharide (LPS)-induced lung injury and necrotic cell challenge, 7E5 treatment markedly reduced neutrophil recruitment and neutrophil extracellular trap (NET) formation. Similarly, the PLG inhibitor tranexamic acid (TXA) attenuated neutrophil recruitment, confirming the critical role of the PLG/PLM system in neutrophil migration. These findings highlight ENO1 as a key regulator of inflammation and neutrophil infiltration. Targeting ENO1 with antibodies could be a promising strategy to mitigate tissue damage caused by excessive neutrophilic inflammation.

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Journal
Immunology
Published
2025-09-09
DOI
https://doi.org/10.1111/imm.70034
Primary Topic
S100 Proteins and Annexins
Type
article
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article

Enolase‐1 Is a Key Regulator of Neutrophil Recruitment During Acute Inflammation

Yu‐Jing Zhuang, Chun‐Jen Chen, Nai‐Yu Chen, Hui‐Wen Chang et al.
Immunology
S100 Proteins and Annexins
article

Enolase‐1 Is a Key Regulator of Neutrophil Recruitment During Acute Inflammation

Yu‐Jing Zhuang, Chun‐Jen Chen, Nai‐Yu Chen, Hui‐Wen Chang, Ting Yuan, Ting‐Wei Lee, P. Huang, Hao Lu
article en

Abstract

Enolase-1 (ENO1) is a moonlighting protein with multiple functions. When expressed on the cell surface, ENO1 binds plasminogen (PLG) and promotes cell migration by facilitating plasmin (PLM)-mediated extracellular matrix degradation. Here, we observed that inflammatory stimulation significantly upregulated ENO1 expression on the neutrophil surface, both in vitro and in vivo. An anti-ENO1 monoclonal antibody (mAb), 7E5, which blocks the ENO1-PLG interaction, effectively suppressed neutrophil invasion in vitro. In mouse models of acute inflammation, including lipopolysaccharide (LPS)-induced lung injury and necrotic cell challenge, 7E5 treatment markedly reduced neutrophil recruitment and neutrophil extracellular trap (NET) formation. Similarly, the PLG inhibitor tranexamic acid (TXA) attenuated neutrophil recruitment, confirming the critical role of the PLG/PLM system in neutrophil migration. These findings highlight ENO1 as a key regulator of inflammation and neutrophil infiltration. Targeting ENO1 with antibodies could be a promising strategy to mitigate tissue damage caused by excessive neutrophilic inflammation.

ImmunologyVol. 177(1)
National Taipei University of Technology (TW), National Taiwan University of Science and Technology (TW), National Taiwan University (TW), Development Center for Biotechnology (TW)
Openalex Percentile: Top 79%
S100 Proteins and Annexins
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