Laboratory of Cell Function Regulation, Department of Biotechnology, College of Life Sciences and Biotechnology, Korea University, Anam-dong, Seongbuk-go, Seoul, 02841, Republic of Korea.
StemLab, Venture Incubation Center Korea University, Seoul, 136-701, Republic of Korea.
Stem Cell Res Ther. 2018 Nov 8;9(1):293. doi: 10.1186/s13287-018-1058-z.
Mesenchymal stem cell-derived conditioned medium (MSC-CM) has emerged as a promising cell-free tool for restoring degenerative diseases and treating traumatic injuries. The present study describes the effect of selenium as a reactive oxygen species (ROS) scavenger and its additive effect with basic fibroblast growth factor (bFGF) on in vitro expansion of amniotic fluid (AF)-MSCs and the paracrine actions of AF-MSC-CM as well as the associated cellular and molecular mechanisms.
In this study, we obtained CM from human AF-MSCs cultured with selenium. The stemness of selenium-treated AF-MSCs was evaluated by cell growth and differentiation potential. Human fibroblasts were treated with AF-MSC-CM and analyzed for cell signaling changes. For in vivo wound healing assay, ICR mice with a full-thickness skin wound were used.
Selenium played a critical role in in vitro expansion of AF-MSCs through activation of the AKT-ERK1/2, Smad2, and Stat3 signaling pathways along with inactivation of GSK3β. When administered together with bFGF, it showed remarkable effect in inhibiting ROS accumulation and preserving their multipotency. Proliferation and migration of human dermal fibroblasts and in vivo wound healing were improved in the CMs derived from AF-MSCs exposed to selenium and bFGF, which was caused by the Smad2, AKT-MEK1/2-ERK, and NFκB signaling triggered by the paracrine factors of AF-MSCs, such as TGF-β, VEGF, and IL-6. Our results suggest the following: (a) supplementation of selenium in AF-MSC culture contributes to in vitro expansion and preservation of multipotency, (b) ROS accumulation causes progressive losses in proliferative and differentiation potential, (c) the separate activities of bFGF and selenium in MSCs exert an additive effect when used together, and (d) the additive combination improves the therapeutic effects of AF-MSC-derived CMs on tissue repair and regeneration.
Antioxidants, such as selenium, should be considered as an essential supplement for eliciting the paracrine effects of MSC-CMs.
间充质干细胞衍生的条件培养基(MSC-CM)作为一种有前途的无细胞工具,已被用于治疗退行性疾病和创伤性损伤。本研究描述了硒作为活性氧(ROS)清除剂的作用及其与碱性成纤维细胞生长因子(bFGF)联合应用对羊膜间充质干细胞(AF-MSCs)体外扩增的影响以及 AF-MSC-CM 的旁分泌作用及其相关的细胞和分子机制。
在这项研究中,我们从培养硒的人羊膜间充质干细胞中获得 CM。通过细胞生长和分化潜能评估硒处理的 AF-MSCs 的干性。用人成纤维细胞处理 AF-MSC-CM,并分析细胞信号变化。为了进行体内伤口愈合实验,我们使用了全层皮肤伤口的 ICR 小鼠。
硒通过激活 AKT-ERK1/2、Smad2 和 Stat3 信号通路以及抑制 GSK3β,在 AF-MSCs 的体外扩增中发挥了关键作用。当与 bFGF 一起使用时,它在抑制 ROS 积累和保持其多能性方面表现出显著效果。暴露于硒和 bFGF 的 AF-MSCs 衍生的 CM 可促进人真皮成纤维细胞的增殖和迁移以及体内伤口愈合,这是由 AF-MSCs 的旁分泌因子(如 TGF-β、VEGF 和 IL-6)触发的 Smad2、AKT-MEK1/2-ERK 和 NFκB 信号引起的。我们的结果表明:(a)在 AF-MSC 培养中补充硒有助于体外扩增和保持多能性;(b)ROS 积累导致增殖和分化潜能逐渐丧失;(c)bFGF 和硒在 MSC 中的单独作用在联合使用时具有相加效应;(d)这种添加剂组合可提高 AF-MSC 衍生的 CM 对组织修复和再生的治疗效果。
抗氧化剂,如硒,应被视为引发 MSC-CM 旁分泌作用的必要补充剂。