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FASEB J. 2017 Aug;31(8):3689-3694. doi: 10.1096/fj.201700149. Epub 2017 May 5.

Altered cargo proteins of human plasma endothelial cell-derived exosomes in atherosclerotic cerebrovascular disease.

Author information

1
Department of Medicine, University of California, San Francisco, San Francisco, California, USA; edward.goetzl@ucsf.edu.
2
Jewish Home of San Francisco, San Francisco, California, USA.
3
Department of Bioengineering, University of California, San Francisco, San Francisco, California, USA.
4
Laboratory of Neurosciences, National Institute on Aging, Baltimore, Maryland, USA.
5
Clinical Translational Science Institute, University of California, San Francisco, San Francisco, California, USA.
6
Department of Neuroscience, University of California, San Diego, La Jolla, California, USA.
7
Department of Pharmacology, University of California, San Diego, La Jolla, California, USA.
8
Sanders-Brown Center on Aging, University of Kentucky, Lexington, Kentucky, USA.

Abstract

Plasma endothelial cell-derived exosomes (EDEs) and platelet-derived exosomes (PDEs) were precipitated and enriched separately by immunospecific absorption procedures for analyses of cargo proteins relevant to atherosclerosis. EDEs had usual exosome size and marker protein content, and significantly higher levels than PDEs of the endothelial proteins vascular cell adhesion molecule-1 (VCAM-1) and endothelial nitric oxide synthase, whereas PDEs had significantly higher levels of platelet glycoprotein VI. EDE levels of VCAM-1, von Willebrand factor, platelet-derived growth factor (PDGF)-BB, angiopoietin-1, and lysyl oxidase-2 and the cerebrovascular-selective proteins glucose transporter 1, permeability-glycoprotein, and large neutral amino acid transporter 1 were significantly higher for 18 patients with cerebrovascular disease (CeVD) than for 18 age- and gender-matched control subjects. PDE levels of PDGF-AA, platelet glycoprotein VI, integrin-linked kinase-1, high mobility group box-1 protein, chemokine CXCL4, and thrombospondin-1 were significantly higher in patients with CeVD than in control subjects, but differences were less with greater overlaps than for EDE proteins. EDE levels of Yes-associated protein (YAP) were higher and of P(S127)-YAP lower in patients with CeVD than in control subjects, consistent with heightened activity of this mechanical force-sensitive system in atherosclerosis. Elevated EDE and PDE levels of atherosclerosis-promoting proteins in CeVD justify clinical studies of their potential value as biomarkers.-Goetzl, E. J., Schwartz, J. B., Mustapic, M., Lobach, I. V., Daneman, R., Abner, E. L., Jicha, G. A. Altered cargo proteins of human plasma endothelial cell-derived exosomes in atherosclerotic cerebrovascular disease.

KEYWORDS:

angiogenesis; blood biomarkers; cellular adhesion; platelets; stroke

PMID:
28476896
PMCID:
PMC5503715
DOI:
10.1096/fj.201700149
[Indexed for MEDLINE]
Free PMC Article

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