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hESC-secreted proteins can be enriched for multiple regenerative therapies by heparin-binding

机译:hESC分泌的蛋白可以通过肝素结合而丰富用于多种再生疗法

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摘要

This work builds upon our findings that proteins secreted by hESCs exhibit pro-regenerative activity, and determines that hESC-conditioned medium robustly enhances the proliferation of both muscle and neural progenitor cells. Importantly, this work establishes that it is the proteins that bind heparin which are responsible for the pro-myogenic effects of hESC-conditioned medium, and indicates that this strategy is suitable for enriching the potentially therapeutic factors. Additionally, this work shows that hESC-secreted proteins act independently of the mitogen FGF-2, and suggests that FGF-2 is unlikely to be a pro-aging molecule in the physiological decline of old muscle repair. Moreover, hESC-secreted factors improve the viability of human cortical neurons in an Alzheimer's disease (AD) model, suggesting that these factors can enhance the maintenance and regeneration of multiple tissues in the aging body.
机译:这项工作建立在我们的发现之上,即hESC分泌的蛋白表现出前再生活性,并确定hESC条件培养基能强有力地增强肌肉和神经祖细胞的增殖。重要的是,这项工作确定了与肝素结合的蛋白质是hESC条件培养基促肌原性作用的原因,并表明该策略适合于丰富潜在的治疗因子。此外,这项工作表明,hESC分泌的蛋白质独立于有丝分裂原FGF-2起作用,并表明FGF-2不太可能是老肌肉修复的生理衰退中的衰老分子。此外,hESC分泌的因子可改善阿尔茨海默病(AD)模型中人类皮质神经元的活力,表明这些因子可增强衰老体内多个组织的维持和再生。

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