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Paracrine effects of adipose-derived stem cells in cutaneous wound healing in streptozotocin-induced diabetic rats

伤口愈合 旁分泌信号 医学 脂肪组织 免疫印迹 血管内皮生长因子 免疫组织化学 染色 病理 男科 链脲佐菌素 糖尿病 内分泌学 内科学 外科 化学 血管内皮生长因子受体 受体 基因 生物化学
作者
Hua Luo,Yongjian Wang,Yongwei Su,Danping Liu,Haijun Xiao,Ming Wu,Yong Zhao,Feng Xue
出处
期刊:Journal of Wound Care [Mark Allen Group]
卷期号:31 (Sup3): S29-S38 被引量:6
标识
DOI:10.12968/jowc.2022.31.sup3.s29
摘要

The purpose of this study was to explore the paracrine effects of adipose-derived stem cells (ASCs) on cutaneous wound healing in diabetic rats.The ASCs were isolated and identified by immunofluorescent staining. The ASCs-conditioned medium (ASCs-CM) was harvested. Cell counting kit (CCK)-8 assay, scratch experiments, western blot and quantitative polymerase chain reaction (qPCR) were performed to observe the effects of ASCs-CM on fibroblasts. A full-thickness skin wound diabetic rat model was prepared, using 34 male, Sprague Dawley rats. ASCs-CM or negative-control medium (N-CM) was injected around the wound surface. The existing wound area was measured on days 4, 8, 12 and 16 after the postoperative day, and the wound tissues were collected for immunohistochemical staining and qPCR quantitative study.In this experiment, the isolated cells were characterised as ASCs. The results of CCK-8 assay, cell scratch test, western blot and qPCR showed ASCs-CM could significantly promote the proliferation, migration and differentiation of fibroblasts. Simultaneously, the healing rate of full-thickness skin wounds in diabetic rats was significantly higher in the ASCs-CM group than the N-CM group on days 4, 8, 12 and 16. Immunohistochemical staining and qPCR results showed that the expression of vascular endothelial growth factor (VEGF, days 4 and 8), α-smooth muscle actin (SMA) (days 4 and 16), transforming growth factor (TGF)-β1 (days 4, 8 and 12) were higher in the ASCs-CM group than that of the N-CM group (p<0.05).This experiment demonstrated that ASCs-CM may accelerate wound healing in diabetic rats by promoting the secretion of TGF-β1, VEGF and the proliferation, migration and differentiation of fibroblasts.

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