Tandem ssDNA in neutrophil extracellular traps binds thrombin and regulates immunothrombosis

• 成果类型: Article
• 署名作者: Guo, Weijie; Huang, Sihao; Shao, Xiangli; Wu, Yuting; Ma, Yuan; Lu, Shuya; Ren, Hanlin; Zhou, Xuening; Yang, Zhenglin; Lyu, Mingkuan; Liu, Yiwei; Gordon, Vernita; Brodbelt, Jennifer S.; Pan, Tao; Lu, Yi
• 署名单位: University of Texas System; University of Texas Austin; University of Texas System; University of Texas Austin; University of Chicago; University of Texas System; University of Texas Austin; University of Texas System; University of Texas Austin
• 刊物名称: PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
• ISSN/ISSBN: 0027-8456
• DOI: 10.1073/pnas.2418191122
• 发表日期: 2025-07-03
• 关键词: mobility shift assay; single-stranded-dna; i-motif dna; cathepsin-g; procoagulant activity; satellite-iii; coagulation; activation; inflammation; inhibitors

摘要

Neutrophils release neutrophil extracellular traps (NETs) to neutralize infections, a process that also contributes to immunothrombosis. While beneficial in localized infections, excessive NET formation can lead to widespread coagulopathy and organ failure. While the roles of NET-associated proteins such as histones in immunothrombosis are well characterized, NET-derived DNAs are much less known. To address this issue, we report herein the direct interaction between thrombin and DNA scaffolds and further, the identification of short tandem repeats of single-stranded (ATTCC)n in NETs that selectively bind thrombin, a crucial enzyme involved in both blood clot formation and immune response. We have also developed a strategy of selective targeting ss(ATTCC)n using antisense locked nucleic acids (LNAs), effectively disrupting NET-thrombin interactions. This finding reveals an unexplored role of single strand DNA (ssDNA) within NETs and provides a broad avenue for developing targeted therapeutic interventions for immunothrombosis-related disorders.