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Detection of pro angiogenic and inflammatory biomarkers in patients with CKD

Cardiovascular disease (CVD) is the most common cause of death in patients with native and post-transplant chronic kidney disease (CKD). To identify new biomarkers of vascular injury and inflammation, we analyzed the proteome of plasma and circulating extracellular vesicles (EVs) in native and post-...

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Autores principales: Jalal, Diana, Sanford, Bridget, Renner, Brandon, Ten Eyck, Patrick, Laskowski, Jennifer, Cooper, James, Sun, Mingyao, Zakharia, Yousef, Spitz, Douglas, Dokun, Ayotunde, Attanasio, Massimo, Jones, Kenneth, Thurman, Joshua M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8062467/
https://www.ncbi.nlm.nih.gov/pubmed/33888746
http://dx.doi.org/10.1038/s41598-021-87710-0
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author Jalal, Diana
Sanford, Bridget
Renner, Brandon
Ten Eyck, Patrick
Laskowski, Jennifer
Cooper, James
Sun, Mingyao
Zakharia, Yousef
Spitz, Douglas
Dokun, Ayotunde
Attanasio, Massimo
Jones, Kenneth
Thurman, Joshua M.
author_facet Jalal, Diana
Sanford, Bridget
Renner, Brandon
Ten Eyck, Patrick
Laskowski, Jennifer
Cooper, James
Sun, Mingyao
Zakharia, Yousef
Spitz, Douglas
Dokun, Ayotunde
Attanasio, Massimo
Jones, Kenneth
Thurman, Joshua M.
author_sort Jalal, Diana
collection PubMed
description Cardiovascular disease (CVD) is the most common cause of death in patients with native and post-transplant chronic kidney disease (CKD). To identify new biomarkers of vascular injury and inflammation, we analyzed the proteome of plasma and circulating extracellular vesicles (EVs) in native and post-transplant CKD patients utilizing an aptamer-based assay. Proteins of angiogenesis were significantly higher in native and post-transplant CKD patients versus healthy controls. Ingenuity pathway analysis (IPA) indicated Ephrin receptor signaling, serine biosynthesis, and transforming growth factor-β as the top pathways activated in both CKD groups. Pro-inflammatory proteins were significantly higher only in the EVs of native CKD patients. IPA indicated acute phase response signaling, insulin-like growth factor-1, tumor necrosis factor-α, and interleukin-6 pathway activation. These data indicate that pathways of angiogenesis and inflammation are activated in CKD patients’ plasma and EVs, respectively. The pathways common in both native and post-transplant CKD may signal similar mechanisms of CVD.
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spelling pubmed-80624672021-04-23 Detection of pro angiogenic and inflammatory biomarkers in patients with CKD Jalal, Diana Sanford, Bridget Renner, Brandon Ten Eyck, Patrick Laskowski, Jennifer Cooper, James Sun, Mingyao Zakharia, Yousef Spitz, Douglas Dokun, Ayotunde Attanasio, Massimo Jones, Kenneth Thurman, Joshua M. Sci Rep Article Cardiovascular disease (CVD) is the most common cause of death in patients with native and post-transplant chronic kidney disease (CKD). To identify new biomarkers of vascular injury and inflammation, we analyzed the proteome of plasma and circulating extracellular vesicles (EVs) in native and post-transplant CKD patients utilizing an aptamer-based assay. Proteins of angiogenesis were significantly higher in native and post-transplant CKD patients versus healthy controls. Ingenuity pathway analysis (IPA) indicated Ephrin receptor signaling, serine biosynthesis, and transforming growth factor-β as the top pathways activated in both CKD groups. Pro-inflammatory proteins were significantly higher only in the EVs of native CKD patients. IPA indicated acute phase response signaling, insulin-like growth factor-1, tumor necrosis factor-α, and interleukin-6 pathway activation. These data indicate that pathways of angiogenesis and inflammation are activated in CKD patients’ plasma and EVs, respectively. The pathways common in both native and post-transplant CKD may signal similar mechanisms of CVD. Nature Publishing Group UK 2021-04-22 /pmc/articles/PMC8062467/ /pubmed/33888746 http://dx.doi.org/10.1038/s41598-021-87710-0 Text en © This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Jalal, Diana
Sanford, Bridget
Renner, Brandon
Ten Eyck, Patrick
Laskowski, Jennifer
Cooper, James
Sun, Mingyao
Zakharia, Yousef
Spitz, Douglas
Dokun, Ayotunde
Attanasio, Massimo
Jones, Kenneth
Thurman, Joshua M.
Detection of pro angiogenic and inflammatory biomarkers in patients with CKD
title Detection of pro angiogenic and inflammatory biomarkers in patients with CKD
title_full Detection of pro angiogenic and inflammatory biomarkers in patients with CKD
title_fullStr Detection of pro angiogenic and inflammatory biomarkers in patients with CKD
title_full_unstemmed Detection of pro angiogenic and inflammatory biomarkers in patients with CKD
title_short Detection of pro angiogenic and inflammatory biomarkers in patients with CKD
title_sort detection of pro angiogenic and inflammatory biomarkers in patients with ckd
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8062467/
https://www.ncbi.nlm.nih.gov/pubmed/33888746
http://dx.doi.org/10.1038/s41598-021-87710-0
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