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First characterization of human amniotic fluid stem cell extracellular vesicles as a powerful paracrine tool endowed with regenerative potential

机译:人类羊水干细胞细胞外囊泡的首次表征为具有再生潜力的强大旁分泌工具

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摘要

Human amniotic fluid stem cells (hAFS) have shown a distinct secretory profile and significant regenerative potential in several preclinical models of disease. Nevertheless, little is known about the detailed characterization of their secretome. Herein we show for the first time that hAFS actively release extracellular vesicles (EV) endowed with significant paracrine potential and regen- erative effect. c-KIT1 hAFS were isolated from leftover samples of amniotic fluid from prenatal screening and stimulated to enhance EV release (24 hours 20% O2 versus 1% O2 preconditioning). The capacity of the c-KIT1 hAFS-derived EV (hAFS-EV) to induce proliferation, survival, immunomo- dulation, and angiogenesis were investigated in vitro and in vivo. The hAFS-EV regenerative poten- tial was also assessed in a model of skeletal muscle atrophy (HSA-Cre, SmnF7/F7 mice), in which mouse AFS transplantation was previously shown to enhance muscle strength and survival. hAFS secreted EV ranged from 50 up to 1,000 nm in size. In vitro analysis defined their role as biological mediators of regenerative, paracrine effects while their modulatory role in decreasing skeletal muscle inflammation in vivo was shown for the first time. Hypoxic preconditioning significantly induced the enrichment of exosomes endowed with regenerative microRNAs within the hAFS-EV. In conclusion, this is the first study showing that c-KIT1 hAFS dynamically release EV endowed with remarkable paracrine potential, thus representing an appealing tool for future regenerative therapy
机译:人类羊水干细胞(hAFS)在几种疾病的临床前模型中显示出独特的分泌特性和显着的再生潜力。然而,人们对其分泌蛋白的详细表征了解甚少。在本文中,我们首次证明了hAFS主动释放具有明显旁分泌潜力和再生作用的细胞外囊泡(EV)。从产前筛查的剩余羊水样本中分离出c-KIT1 hAFS,并对其刺激以增强EV释放(24小时20%O2与1%O2预处理)。在体外和体内研究了c-KIT1 hAFS衍生的EV(hAFS-EV)诱导增殖,存活,免疫调节和血管生成的能力。在骨骼肌萎缩模型(HSA-Cre,SmnF7 / F7小鼠)中也评估了hAFS-EV的再生潜能,其中先前证明了小鼠AFS移植可增强肌肉强度和存活率。 hAFS分泌的EV大小在50到1,000 nm之间。体外分析定义了它们作为再生,旁分泌作用的生物介质的作用,而首次显示了它们在体内减少骨骼肌炎症的调节作用。缺氧预处理显着诱导了hAFS-EV中具有再生microRNA的外泌体的富集。总之,这是第一项研究,表明c-KIT1 hAFS动态释放具有显着旁分泌潜力的EV,因此代表了未来再生疗法的诱人工具

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