Zhang Yiyao, Zhang Peng, Gao Xiuqiu, Chang Linna, Chen Zhenhua, Mei Xifan
Jinzhou Medical University, Jinzhou 121001, People's Republic of China.
Jinzhou Medical University, Jinzhou 121001, People's Republic of China.
Mater Sci Eng C Mater Biol Appl. 2021 Jan;120:111671. doi: 10.1016/j.msec.2020.111671. Epub 2020 Oct 22.
Exosomes derived from human umbilical cord mesenchymal stem cells (HUCMSCs) were helpful for injury repair, but whether HUCMSCs-derived exosomes could be encapsulated in a novel nanohydrogel to regulate diabetic wound healing was unclear. Here, HUCMSCs-derived exosomes encapsulated in a bioactive scaffold composed of polyvinyl alcohol (PVA)/alginate (Alg) nanohydrogel (exo@H) was applied to wound healing of diabetic rats. Results found that exo@H could facilitate the proliferation, migration and angiogenesis of HUVECs and sped up the process of diabetic wound healing. We confirmed that exo@H contributed to the expression of the molecules related to wound healing, including SMA, SR-B1 and CD31. Besides, we also found that exo@H up-regulated VEGF level via regulating ERK1/2 pathway. These data demonstrated that exo@H significantly accelerated healing of diabetic wounds in rats by promoting angiogenesis.
源自人脐带间充质干细胞(HUCMSCs)的外泌体有助于损伤修复,但HUCMSCs衍生的外泌体是否可以封装在新型纳米水凝胶中以调节糖尿病伤口愈合尚不清楚。在此,将封装在由聚乙烯醇(PVA)/藻酸盐(Alg)纳米水凝胶组成的生物活性支架(exo@H)中的HUCMSCs衍生的外泌体应用于糖尿病大鼠的伤口愈合。结果发现,exo@H可促进人脐静脉内皮细胞(HUVECs)的增殖、迁移和血管生成,并加速糖尿病伤口愈合过程。我们证实,exo@H有助于与伤口愈合相关分子的表达,包括平滑肌肌动蛋白(SMA)、清道夫受体B1(SR-B1)和血小板内皮细胞黏附分子-1(CD31)。此外,我们还发现exo@H通过调节细胞外信号调节激酶1/2(ERK1/2)通路上调血管内皮生长因子(VEGF)水平。这些数据表明,exo@H通过促进血管生成显著加速了大鼠糖尿病伤口的愈合。