Nanovesicles engineered from ES cells for enhanced cell proliferation

被引:84
作者
Jeong, Dayeong [1 ]
Jo, Wonju [2 ]
Yoon, Jaewoong [2 ]
Kim, Junho [1 ]
Gianchandani, Sachi [3 ]
Gho, Yong Song [4 ]
Park, Jaesung [1 ,2 ]
机构
[1] POSTECH, Sch Interdisciplinary Biosci & Bioengn, Pohang 790784, Gyeongbuk, South Korea
[2] POSTECH, Dept Mech Engn, Pohang 790784, Gyeongbuk, South Korea
[3] Univ Michigan, Sch Kinesiol, Ann Arbor, MI 48109 USA
[4] POSTECH, Dept Life Sci, Pohang 790784, Gyeongbuk, South Korea
基金
新加坡国家研究基金会;
关键词
Nanoparticles; Cell proliferation; ECM; Fibroblasts; Growth factor; Stem cell; STEM-CELLS; IN-VITRO; ENDOTHELIAL-CELLS; HORIZONTAL TRANSFER; MESSENGER-RNAS; MICROVESICLES; MIGRATION; DELIVERY; GROWTH; TISSUE;
D O I
10.1016/j.biomaterials.2014.07.047
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
Extracellular vesicles (Exosomes and microvesicles) have drawn wide attentions in both diagnostic and therapeutic applications, since they are considered to shuttle biological signals intercellularly. However, further research on exosomes is limited by their rarity and heterogeneity even after lengthy isolation processes. In particular, these limitations are challenging in therapeutic applications. To meet these demands, cell-derived nanovesicles that mimic exosomes were generated by extruding living embryonic stem cells through micro-filters. These nanovesicles have an enclosed lipid bilayer and contain cellular contents. The present study investigated the ability of these nanovesicles to improve proliferation by treating primary murine skin fibroblasts with the nanovesicles. The treated skin fibroblasts showed higher expression levels of mRNA, VEGF-alpha, protein levels of TGF-beta collagen I, PCNA, and Ki-67, as well as enhanced cell proliferation rate and number, compared to non-treated cells. The results indicate that treatment with the nanovesicles could potentially contribute to recovery or wound healing process of tissues. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:9302 / 9310
页数:9
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