Projects per year
Abstract
Background: Vascular cell adhesion molecule-1 (VCAM-1+) endothelial cell-derived extracellular vesicles (EC-EVs) are augmented in cardiovascular disease, where they can signal the deployment of immune cells from the splenic reserve. Endothelial cells in culture activated with pro-inflammatory tumor necrosis factor-α (TNF-a) also release VCAM-1+ EC-EVs. However, isolating VCAM-1+ EC-EVs from conditioned cell culture media for subsequent in-depth analysis remains challenging. Aim: We utilized the extracellular vesicles (EV) microfluidics herringbone chip (EVHB-Chip), coated with anti-VCAM-1 antibodies, for selective capture of VCAM-1+ cells and EC-EVs. Methods and Results: Engineered EA.hy926 endothelial cells overexpressing VCAM-1 (P < 0.001 versus control) showed increased binding to the VCAM-1-EV HB-Chip versus an IgG device. TNF-α-stimulated human umbilical cord vein endothelial cells (HUVECs) exhibited elevated VCAM-1 protein levels (P < 0.001) and preferential binding to the VCAM-1-EV HB-Chip versus the IgG device. HUVECs stimulated with TNF-α showed differential gene expression of intercellular adhesion molecule-1 (ICAM-1) (P < 0.001) and VCAM-1 (P < 0.001) by digital droplet PCR versus control cells. HUVEC-derived EC-EVs were positive for CD9, CD63, HSP70, and ALIX and had a modal size of 83.5 nm. Control and TNF-α-stimulated HUVEC-derived EC-EV cultures were captured on the VCAM-1-EV HB-Chip, demonstrating selective capture. VCAM-1+ EC-EV were significantly enriched for ICAM-1 (P < 0.001) mRNA transcripts. Conclusion: This study presents a novel approach using theEV HB-Chip, coated with anti-VCAM-1 antibodies and digital droplet PCR for the study of VCAM-1+ EC-EVs. Isolation of VCAM-1+ EC-EV from heterogeneous sources such as conditioned cell culture media holds promise for subsequent detailed characterization, and may facilitate the study of VCAM-1+ EC-EVs in cardiovascular and metabolic diseases, for disease monitoring and therapeutic insights.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 83-94 |
| Number of pages | 12 |
| Journal | Extracellular Vesicles and Circulating Nucleic Acids |
| Volume | 5 |
| Issue number | 1 |
| DOIs | |
| State | Published - 2024 |
Bibliographical note
Publisher Copyright:© The Author(s) 2024.
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
-
SDG 3 Good Health and Well-being
Keywords
- atherosclerosis
- biomarker
- Cardiovascular
- endothelium
- inflammation
- vascular
PubMed: MeSH publication types
- Journal Article
Fingerprint
Dive into the research topics of 'The isolation of VCAM-1+ endothelial cell-derived extracellular vesicles using microfluidics'. Together they form a unique fingerprint.Projects
- 1 Active
-
ATP-Bio: NSF Engineering Research Center for Advanced Technologies for the Preservation of Biological Systems (ATP-Bio)
Bischof, J. C. (PI), Toner, M. (CoPI), Aguilar, G. (CoPI), Healy, K. E. (CoPI), Uygun, K. (Key Personnel), Burger, A. A. (Project Manager), Wolf, S. M. (Key Personnel), Roehrig, G. H. (Key Personnel), Heremans, C. (Coordinator), McAlpine, M. (Key Personnel), Mangolini, L. (Key Personnel), Uygun, B. E. (Key Personnel), Finger, E. B. (Key Personnel), Garwood, M. (Key Personnel), Dames, C. (Key Personnel), Powell-Palm, M. J. (Key Personnel), Franklin, R. R. (Key Personnel), Singh, B. N. (Key Personnel), Yin, Y. (Key Personnel), Usta, O. B. (Key Personnel), Rubinsky, B. (Key Personnel), Tessier, S. N. (Key Personnel), Sandlin, R. D. (Key Personnel), Kangas, J. R. (Key Personnel), Iaizzo, P. A. (Key Personnel), Irimia, D. (Key Personnel), Ogle, B. M. (Key Personnel), Stadler, B. J. (Key Personnel), Bangalore Kodandaramaiah, S. (Key Personnel), Aksan, A. (Key Personnel) & Rabin, Y. (Key Personnel)
9/1/20 → 8/31/30
Project: Research and Outreach Center
Cite this
- APA
- Standard
- Harvard
- Vancouver
- Author
- BIBTEX
- RIS