312 Neutrophil Extracellular Trap (NET) Proteins Enriched in Emboli Retrieved from Stroke Patients with Atrial Fibrillation. (April 2023)
- Record Type:
- Journal Article
- Title:
- 312 Neutrophil Extracellular Trap (NET) Proteins Enriched in Emboli Retrieved from Stroke Patients with Atrial Fibrillation. (April 2023)
- Main Title:
- 312 Neutrophil Extracellular Trap (NET) Proteins Enriched in Emboli Retrieved from Stroke Patients with Atrial Fibrillation
- Authors:
- Akkipeddi, Sajal Medha
Rahmani, Redi
Schartz, Derrek
Chittaranjan, Siddharth
Gunturi, Aditya
Bhalla, Tarun
Mattingly, Thomas
Morrell, Craig
Bender, Matthew T. - Abstract:
- Abstract : INTRODUCTION: Recent literature has demonstrated remarkable heterogeneity in the composition of acute ischemic stroke (AIS) emboli from different etiologies, which may directly impact their susceptibility to current standard-of-care therapies. METHODS: The full proteomic composition of retrieved thromboembolic material from 24 patients with AIS was evaluated by mass spectrometry. Of the 1797 total proteins identified, 88 known marker proteins were sorted into groups representing broad classes of embolus components: RBCs, PLTs, PMNs, histones, complement proteins, and other clotting-associated proteins (e.g., fibrinogen). The abundance of individual proteins in patients with AF was compared to that of patients without AF using Mann-Whitney U-tests, with significant differences described by the fold change (FC) in abundance. Functional implications of identified differences were explored using the Gene Ontology (GO) enRIchment anaLysis and visuaLizAtion tool (GOrilla). RESULTS: There were no significant differences in protein abundance in the RBC, complement, or clotting-associated protein groups. One out of the 11 PLT group proteins (p = 0.042, FC = 2.46), eight out of the 15 PMN group proteins (p < 0.05, FC > 2), and four out of the 14 histone proteins were significantly enriched in emboli from patients with AF (p < 0.05, FC > 2). The most significantly represented functional GO pathways in patients with AF involved PMN activation and degranulation (p < 10-7).Abstract : INTRODUCTION: Recent literature has demonstrated remarkable heterogeneity in the composition of acute ischemic stroke (AIS) emboli from different etiologies, which may directly impact their susceptibility to current standard-of-care therapies. METHODS: The full proteomic composition of retrieved thromboembolic material from 24 patients with AIS was evaluated by mass spectrometry. Of the 1797 total proteins identified, 88 known marker proteins were sorted into groups representing broad classes of embolus components: RBCs, PLTs, PMNs, histones, complement proteins, and other clotting-associated proteins (e.g., fibrinogen). The abundance of individual proteins in patients with AF was compared to that of patients without AF using Mann-Whitney U-tests, with significant differences described by the fold change (FC) in abundance. Functional implications of identified differences were explored using the Gene Ontology (GO) enRIchment anaLysis and visuaLizAtion tool (GOrilla). RESULTS: There were no significant differences in protein abundance in the RBC, complement, or clotting-associated protein groups. One out of the 11 PLT group proteins (p = 0.042, FC = 2.46), eight out of the 15 PMN group proteins (p < 0.05, FC > 2), and four out of the 14 histone proteins were significantly enriched in emboli from patients with AF (p < 0.05, FC > 2). The most significantly represented functional GO pathways in patients with AF involved PMN activation and degranulation (p < 10-7). CONCLUSIONS: The enrichment of PMN proteins and histones, as well as pathways culminating in PMN activation and degranulation, suggests the presence of neutrophil extracellular traps (NETs) in emboli of stroke patients with AF. NETs are a significant though understudied structural component of clots, and so this work hints at not only significant pathological immunothrombosis in patients with AF, but also at potential therapeutic targets for AIS in this population. … (more)
- Is Part Of:
- Neurosurgery. Volume 69(2023)Supplement 1
- Journal:
- Neurosurgery
- Issue:
- Volume 69(2023)Supplement 1
- Issue Display:
- Volume 69, Issue 1 (2023)
- Year:
- 2023
- Volume:
- 69
- Issue:
- 1
- Issue Sort Value:
- 2023-0069-0001-0000
- Page Start:
- 43
- Page End:
- 43
- Publication Date:
- 2023-04
- Subjects:
- Nervous system -- Surgery -- Periodicals
617.48005 - Journal URLs:
- https://academic.oup.com/neurosurgery ↗
http://www.neurosurgery-online.com ↗
https://journals.lww.com/neurosurgery/pages/default.aspx ↗
http://journals.lww.com ↗ - DOI:
- 10.1227/neu.0000000000002375_312 ↗
- Languages:
- English
- ISSNs:
- 0148-396X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6081.582000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 26179.xml