Comprehensive Proteomic Analysis of Mesenchymal Stem Cell Exosomes Reveals Modulation of Angiogenesis via Nuclear Factor-KappaB Signaling

Johnathon D. Anderson(University of California, Davis), Henrik J. Johansson(Karolinska Institutet), Calvin S. Graham(University of California, Davis), Mattias Vesterlund(Karolinska Institutet), Missy T. Pham(University of California, Davis), Charles Bramlett(University of California, Davis), Elizabeth N. Montgomery(University of California, Davis), Matt Mellema(University of California, Davis), Renee L. Bardini(University of California, Davis), Zelenia Contreras(University of California, Davis), Madeline Hoon(University of California, Davis), Gerhard Bauer(University of California, Davis), Kyle D. Fink(University of California, Davis), Brian Fury(University of California, Davis), Kyle Hendrix(University of California, Davis), Frédéric Chédin(University of California, Davis), Samir EL Andaloussi(Karolinska Institutet), Billie Hwang(University of Washington), Michael S. Mulligan(University of Washington), Janne Lehtiö(Karolinska Institutet), Jan A. Nolta(University of California, Davis)
Stem Cells
January 19, 2016
Cited by 539Open Access
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Abstract

Mesenchymal stem cells (MSC) are known to facilitate healing of ischemic tissue related diseases through proangiogenic secretory proteins. Recent studies further show that MSC derived exosomes function as paracrine effectors of angiogenesis, however, the identity of which components of the exosome proteome responsible for this effect remains elusive. To address this we used high-resolution isoelectric focusing coupled liquid chromatography tandem mass spectrometry, an unbiased high throughput proteomics approach to comprehensively characterize the proteinaceous contents of MSCs and MSC derived exosomes. We probed the proteome of MSCs and MSC derived exosomes from cells cultured under expansion conditions and under ischemic tissue simulated conditions to elucidate key angiogenic paracrine effectors present and potentially differentially expressed in these conditions. In total, 6,342 proteins were identified in MSCs and 1,927 proteins in MSC derived exosomes, representing to our knowledge the first time these proteomes have been probed comprehensively. Multilayered analyses identified several putative paracrine effectors of angiogenesis present in MSC exosomes and increased in expression in MSCs exposed to ischemic tissue-simulated conditions; these include platelet derived growth factor, epidermal growth factor, fibroblast growth factor, and most notably nuclear factor-kappaB (NFkB) signaling pathway proteins. NFkB signaling was identified as a key mediator of MSC exosome induced angiogenesis in endothelial cells by functional in vitro validation using a specific inhibitor. Collectively, the results of our proteomic analysis show that MSC derived exosomes contain a robust profile of angiogenic paracrine effectors, which have potential for the treatment of ischemic tissue-related diseases.


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