Human umbilical cord mesenchymal stem cells implantation accelerates cutaneous wound healing in diabetic rats via the Wnt signaling pathway

被引:42
|
作者
Han, Yanfu [1 ]
Sun, Tianjun [2 ]
Han, Yanqing [3 ]
Lin, Lingling [4 ]
Liu, Chang [1 ]
Liu, Jing [1 ]
Yan, Guangzhi [4 ]
Tao, Ran [5 ]
机构
[1] Capital Med Univ, Beijing Shijitan Hosp, Dept Plast Surg, 10 Tieyilu, Beijing 100038, Peoples R China
[2] Peoples Liberat Army Gen Hosp, Dept Burn & Plast Surg, Hainan Branch, Haitangwan, Sanya, Peoples R China
[3] Wuhan Inst Technol, Sch Elect & Informat Engn, 366 Huquan, Wuhan, Hubei, Peoples R China
[4] Harrison Int Peace Hosp, Dept Burn & Plast Surg, 180 Renmin East Rd, Hengshui, Hebei, Peoples R China
[5] Peoples Liberat Army Gen Hosp, Dept Plast Surg, 28 Fuxing Rd, Beijing, Peoples R China
关键词
Mesenchymal stem cell therapy; Tissue engineering skin; Diabetes mellitus; Wound healing; Wnt signaling pathway; EPIDEMIOLOGY;
D O I
10.1186/s40001-019-0366-9
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
ObjectiveDifficulty in wound healing is one common complication of diabetes mellitus. The study explored whether the therapeutic effect of human umbilical cord mesenchymal stem cells (hUCMSCs) on diabetic ulcer wound was enhanced by the activation of the Wnt signaling pathway.MethodsRat diabetic model was established by intraperitoneal injection of Streptozotocin (STZ). hUCMSCs were purified and seeded on the collagen-chitosan laser drilling acellular dermal matrix (CCLDADM) scaffold, which was subsequently implanted into the cutaneous wound of normal and diabetic rats, followed by daily injection of Wnt signaling pathway agonist (Wnt3a) or antagonist (sFRP3) at the edge of the scaffold. Wound healing was checked on days 7, 14, and 21, and the fibrous tissue deposition, capillaries, and epidermal regeneration at the wound were examined by hematoxylin-eosin staining. The hUCMSCs-CCLDADM scaffold was cultured in vitro and treated with Wnt3a or sFRP3, followed by evaluation of cell proliferation, cell proliferation rate, survival status, and altered protein levels in the Wnt signaling pathway using BrdU staining, CCK-8 assay, live/dead staining, and Western blotting, respectively.ResultsOn days 7 and 14 postoperatively, the speed of wound healing was significantly lower in diabetic rats than that in normal control rats. This phenomenon was significantly improved by the activation of the Wnt signaling pathway that also elevated the fibrous protein deposition and the abundance of capillary in the granulation tissue. Conversely, blockade of Wnt signaling slowed the healing of skin wound in diabetic rats. The activation of Wnt signaling pathway promoted the proliferation and differentiation and decreased the apoptosis of hUCMSCs, thereby elevating the number of living hUCMSCs on the CCLDADM scaffold, while the suppression exerted a contrary effect.ConclusionThe activation of the Wnt signaling pathway promotes the healing of diabetic skin wound by the regulation of proliferation and differentiation of hUCMSCs on the CCLDADM scaffold.
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页数:9
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