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Exosomes released from human induced pluripotent stem cells-derived MSCs facilitate cutaneous wound healing by promoting collagen synthesis and angiogenesis.

作者信息

Zhang Jieyuan, Guan Junjie, Niu Xin, Hu Guowen, Guo Shangchun, Li Qing, Xie Zongping, Zhang Changqing, Wang Yang

机构信息

Department of Orthopedic Surgery, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai, China.

Institute of Microsurgery on Extremities, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai, China.

出版信息

J Transl Med. 2015 Feb 1;13:49. doi: 10.1186/s12967-015-0417-0.


DOI:10.1186/s12967-015-0417-0
PMID:25638205
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4371881/
Abstract

BACKGROUND: Human induced pluripotent stem cell-derived mesenchymal stem cells (hiPSC-MSCs) have emerged as a promising alternative for stem cell transplantation therapy. Exosomes derived from mesenchymal stem cells (MSC-Exos) can play important roles in repairing injured tissues. However, to date, no reports have demonstrated the use of hiPSC-MSC-Exos in cutaneous wound healing, and little is known regarding their underlying mechanisms in tissue repair. METHODS: hiPSC-MSC-Exos were injected subcutaneously around wound sites in a rat model and the efficacy of hiPSC-MSC-Exos was assessed by measuring wound closure areas, by histological and immunofluorescence examinations. We also evaluated the in vitro effects of hiPSC-MSC-Exos on both the proliferation and migration of human dermal fibroblasts and human umbilical vein endothelial cells (HUVECs) by cell-counting and scratch assays, respectively. The effects of exosomes on fibroblast collagen and elastin secretion were studied in enzyme-linked immunosorbent assays and quantitative reverse-transcriptase-polymerase chain reaction (qRT-PCR). In vitro capillary network formation was determined in tube-formation assays. RESULTS: Transplanting hiPSC-MSC-Exos to wound sites resulted in accelerated re-epithelialization, reduced scar widths, and the promotion of collagen maturity. Moreover, hiPSC-MSC-Exos not only promoted the generation of newly formed vessels, but also accelerated their maturation in wound sites. We found that hiPSC-MSC-Exos stimulated the proliferation and migration of human dermal fibroblasts and HUVECs in a dose-dependent manner in vitro. Similarly, Type I, III collagen and elastin secretion and mRNA expression by fibroblasts and tube formation by HUVECs were also increased with increasing hiPSC-MSC-Exos concentrations. CONCLUSIONS: Our findings suggest that hiPSC-MSC-Exos can facilitate cutaneous wound healing by promoting collagen synthesis and angiogenesis. These data provide the first evidence for the potential of hiPSC-MSC-Exos in treating cutaneous wounds.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3fd/4371881/d88a7529bffa/12967_2015_417_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3fd/4371881/e3204b09ecc1/12967_2015_417_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3fd/4371881/d5a6362fe12c/12967_2015_417_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3fd/4371881/b1d87ea69794/12967_2015_417_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3fd/4371881/3c07c9d6b510/12967_2015_417_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3fd/4371881/8da7e70f1352/12967_2015_417_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3fd/4371881/b59a655de10b/12967_2015_417_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3fd/4371881/d88a7529bffa/12967_2015_417_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3fd/4371881/e3204b09ecc1/12967_2015_417_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3fd/4371881/d5a6362fe12c/12967_2015_417_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3fd/4371881/b1d87ea69794/12967_2015_417_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3fd/4371881/3c07c9d6b510/12967_2015_417_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3fd/4371881/8da7e70f1352/12967_2015_417_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3fd/4371881/b59a655de10b/12967_2015_417_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3fd/4371881/d88a7529bffa/12967_2015_417_Fig7_HTML.jpg

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[9]
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[10]
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本文引用的文献

[1]
Conditioned medium from hypoxic bone marrow-derived mesenchymal stem cells enhances wound healing in mice.

PLoS One. 2014-4-29

[2]
Extracellular vesicles derived from human bone marrow mesenchymal stem cells promote angiogenesis in a rat myocardial infarction model.

J Mol Med (Berl). 2013-12-14

[3]
Mesenchymal stem cell-like cells derived from mouse induced pluripotent stem cells ameliorate diabetic polyneuropathy in mice.

Biomed Res Int. 2013-11-11

[4]
The paracrine effects of mesenchymal stem cells stimulate the regeneration capacity of endogenous stem cells in the repair of a bladder-outlet-obstruction-induced overactive bladder.

Stem Cells Dev. 2014-3-15

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Enhanced wound healing by topical administration of mesenchymal stem cells transfected with stromal cell-derived factor-1.

Biomaterials. 2013-9-17

[6]
The healing effect of stem cells loaded in nanofibrous scaffolds on full thickness skin defects.

J Biomed Nanotechnol. 2013-9

[7]
Reprogramming of mesenchymal stem cells derived from iPSCs seeded on biofunctionalized calcium phosphate scaffold for bone engineering.

Biomaterials. 2013-7-24

[8]
A simple method for deriving functional MSCs and applied for osteogenesis in 3D scaffolds.

Sci Rep. 2013

[9]
Methods of analysis of dendritic cell-derived exosome-shuttle microRNA and its horizontal propagation between dendritic cells.

Methods Mol Biol. 2013

[10]
Functional analysis of exosomal microRNA in cell-cell communication research.

Methods Mol Biol. 2013

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