Mesenchymal stromal cells of human umbilical cord Wharton's jelly accelerate wound healing by paracrine mechanisms

被引:88
|
作者
Shohara, Ryutaro
Yamamoto, Akihito [1 ]
Takikawa, Sachiko [2 ]
Iwase, Akira [2 ]
Hibi, Hideharu
Kikkawa, Fumitaka [2 ]
Ueda, Minoru
机构
[1] Nagoya Univ, Grad Sch Med, Dept Oral & Maxillofacial Surg, Showa Ku, Nagoya, Aichi 4668550, Japan
[2] Nagoya Univ, Dept Obstet & Gynecol, Nagoya, Aichi 4668550, Japan
关键词
human umbilical cord perivascular cells; wound healing; mesenchymal stromal cells; anti-inflammatory M2 macrophage; STEM-CELLS; BONE-MARROW; ACTIVATED MACROPHAGES; M2; MACROPHAGES; DIFFERENTIATION; ANGIOGENESIS; PHENOTYPE; MURINE; REPAIR; REGENERATION;
D O I
10.3109/14653249.2012.706705
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Background aims. Mesenchymal stromal cells (MSC) can be isolated from the perivascular connective tissue of umbilical cords, called Wharton's jelly. These human umbilical cord perivascular cells (HUCPVC) might provide therapeutic benefits when treating skeletal or cutaneous malformations in neonatal patients. Methods. HUCPVC were isolated, and their proliferation rate, marker expression and multilineage differentiation potential determined. HUCPVC or their conditioned medium (HUCPVC-CM) was injected into the excisional wound of a mouse splinted-wound model. The effects of the treatment on wound closure were examined by morphohistochemical and gene expression analyses. Results. HUCPVC expressed typical MSC markers and could differentiate into osteoblastic and adipogenic lineages. HUCPVC transplanted into the mouse wound accelerated wound closure. Immunohistologic analysis showed that the HUCPVC accelerated wound healing by enhancing collagen deposition and angiogenesis via paracrine mechanisms. Furthermore, treatment with HUCPVC-CM alone significantly enhanced wound closure. HUCPVC-CM increased the number of anti-inflammatory M2 macrophages expressing resistin-like molecule (RELM)-alpha/CD11b and promoted neovessel maturation. Quantitative polymerase chain reaction (PCR) analysis showed that HUCPVC-CM increased the expression of tissue-repairing cytokines interleukin (IL)-10, transforming growth factor (TGF)-beta 1, vascular endothelial growth factor (VEGF)-1 and angiopoietin-1 at the healing wound. Conclusions. Our results show that HUCPVC promotes wound healing via multifaceted paracrine mechanisms. Together with their ability to differentiate into the osteogenic linage, HUCPVC may provide significant therapeutic benefits for treating wounds in neonatal patients.
引用
收藏
页码:1171 / 1181
页数:11
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