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DHP-Derivative and Low Oxygen Tension Effectively Induces Human Adipose Stromal Cell Reprogramming

机译:DHP衍生物和低氧张力有效诱导人类脂肪基质细胞重编程

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摘要

Background and MethodsIn this study, we utilized a combination of low oxygen tension and a novel anti-oxidant, 4-(3,4-dihydroxy-phenyl)-derivative (DHP-d) to directly induce adipose tissue stromal cells (ATSC) to de-differentiate into more primitive stem cells. De-differentiated ATSCs was overexpress stemness genes, Rex-1, Oct-4, Sox-2, and Nanog. Additionally, demethylation of the regulatory regions of Rex-1, stemnesses, and HIF1α and scavenging of reactive oxygen species were finally resulted in an improved stem cell behavior of de-differentiate ATSC (de-ATSC). Proliferation activity of ATSCs after dedifferentiation was induced by REX1, Oct4, and JAK/STAT3 directly or indirectly. De-ATSCs showed increased migration activity that mediated by P38/JUNK and ERK phosphorylation. Moreover, regenerative efficacy of de-ATSC engrafted spinal cord-injured rats and chemical-induced diabetes animals were significantly restored their functions.
机译:背景与方法在这项研究中,我们利用低氧张力和新型抗氧化剂4-(3,4-二羟基-苯基)-衍生物(DHP-d)的组合直接诱导脂肪组织基质细胞(ATSC)去分化成更多原始干细胞。去分化的ATSCs是过表达茎基因,Rex-1,Oct-4,Sox-2和Nanog。此外,Rex-1,茎和HIF1α调控区的去甲基化以及对活性氧的清除最终改善了去分化ATSC(de-ATSC)的干细胞行为。 REX1,Oct4和JAK / STAT3直接或间接诱导去分化后ATSC的增殖活性。 De-ATSCs显示出由P38 / JUNK和ERK磷酸化介导的迁移活性增加。而且,去ATSC移植的脊髓损伤大鼠和化学诱导的糖尿病动物的再生功效显着恢复了其功能。

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