Neutrophil CD14 is a driver and a therapeutic target for deep vein thrombosis
Neutrophil-mediated persistent inflammation and neutrophil extracellular trap formation (NETosis) are critical in the pathogenesis of deep vein thrombosis (DVT). Identifying the mechanisms controlling these proinflammatory and prothrombotic functions is critical for designing and developing new therapeutics for DVT. However, how neutrophils acquire these phenotypes during the early stages of DVT remains poorly understood. Here, multiomic analyses (RNA sequencing, proteomics, and flow cytometry) of bone-marrow neutrophils 3 hours after DVT, revealed consistent overexpression of CD14. Concurrently, mice with DVT exhibited significantly elevated plasma granulocyte colony-stimulating factor (G-CSF) and neutrophil hyperactivation. Mechanistic studies using a geometric deep learning model (DeepPBS) and chromatin immunoprecipitation revealed that elevated G-CSF drives CD14 overexpression by upregulating the transcription factor C/EBPα (leucine zipper CCAAT-enhancer binding protein α). Importantly, neutrophil-specific CD14 knockdown using a novel lentiviral short hairpin RNA approach significantly improved DVT outcomes by lowering thrombus burden, thrombosis incidence, and intrathrombus neutrophil and citrullinated histone H3 accumulation. Studies in G-CSF stimulated primary human neutrophils revealed that CD14 inhibition reduces markers of inflammation and NETosis (activated gasdermin D, citrullinated histone H3, and S100A8/A9), while increasing apoptosis, thus demonstrating translational relevance. Collectively, our study uncovers an essential role of neutrophil CD14 in DVT pathogenesis and establishes it as a promising therapeutic target for DVT.
Authors
- Gurranna Male (ORCID: https://orcid.org/0000-0003-2544-6626)
- Tarek Magdy (ORCID: https://orcid.org/0000-0002-4790-490X)
- Sumit Kumar Anand (ORCID: https://orcid.org/0000-0003-3719-0744)
- Sumati Rohilla (ORCID: https://orcid.org/0000-0002-0860-0188)
- Raktim Mitra (ORCID: https://orcid.org/0000-0003-1182-3742)
- Nirvana Shaaban (ORCID: https://orcid.org/0009-0004-7463-4089)
- Arif Yurdagul (ORCID: https://orcid.org/0000-0002-7613-6313)
- Rajan Pandit (ORCID: https://orcid.org/0000-0001-9744-1248)
- X H Zhang
- Karen Y. Stokes (ORCID: https://orcid.org/0000-0002-7612-3467)
- Harpreet Kaur (ORCID: https://orcid.org/0000-0001-7800-0076)
- Sandeep Das (ORCID: https://orcid.org/0000-0002-6722-3909)
- Alexa Martinez (ORCID: https://orcid.org/0000-0001-9376-5368)
- Dhiraj Kumar (ORCID: https://orcid.org/0000-0001-7578-2930)
- Nirav Dhanesha (ORCID: https://orcid.org/0000-0001-9268-4363)
- Evan J Kidder
- Lakshmi Chandaluri
- Amdadul Huque (ORCID: https://orcid.org/0000-0002-3895-9378)
- Oren Rom
- David S Gross
- Dweipayan Goswami
- Amr R Salem
- A. Wayne Orr
- Louise Frausto
- Sultan Tousif
- Nilesh Pandey
- Megan Butler
- Suman Mohajan
Institutions
- Gujarat University (IN)
- University of Washington (US)
- Protein Research Foundation (JP)
- Louisiana State University Health Sciences Center Shreveport (US)
Publication Details
- Journal
- Blood Advances
- Published
- 2026-01-09
- DOI
- https://doi.org/10.1182/bloodadvances.2025017224
- Citations
- 1
- Primary Topic
- Neutrophil, Myeloperoxidase and Oxidative Mechanisms
- Type
- article
- Field-Weighted Citation Impact
- 24.43
Funders
- National Science Foundation
- American Heart Association
- National Institutes of Health
- National Heart, Lung, and Blood Institute
- National Institute of General Medical Sciences