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.
Abstract
AbstractCardiovascular 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.
Funder
American Heart Association
National Institutes of Health
Publisher
Springer Science and Business Media LLC
Cited by
19 articles.
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