<i>Tremella fuciformis</i> polysaccharide: enhancing ischemic hypoxic adaptation of mesenchymal stem cells.

IF 1.8 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Lei Yang, Shan Chen, Gang Zhao, Wei Gou, Weiwei Wang, Zhipeng Hu
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引用次数: 0

Abstract

Human Placenta-Derived Mesenchymal Stem Cells (HP-MSCs) are recognized for their potential in treating various diseases due to their multidirectional differentiation and immunomodulatory abilities. However, the therapeutic efficacy is often compromised in ischemic and hypoxic environments. Tremella Fuciformis Polysaccharide (TFP), a natural polysaccharide known for its immunomodulatory and anti-inflammatory properties, stands a good chance of overcoming this limitation. Our study investigates whether TFP enhances the therapeutic efficacy of HP-MSCs under ischemic-hypoxic conditions by inhibiting autophagy, with a focus on the role of the ERK signaling pathway. HP-MSCs were cultured under hypoxic conditions to simulate an ischemic environment and TFP was added to investigate its effects on MSC bioactivity, apoptosis, and proliferation. Mechanistic studies were conducted to assess the activation of the ERK signaling pathway and the expression of autophagy-related markers. TFP enhanced HP-MSC bioactivity under hypoxia by reducing apoptosis and promoting proliferation. Mechanistic analysis revealed that TFP enhanced the ability of HP-MSCs to adapt to hypoxic stress by activating the ERK signaling pathway. This activation led to the inhibition of autophagy-related markers, suggesting that TFP plays a protective role in hypoxia-induced cell stress. TFP enhances the therapeutic potential of HP-MSCs in ischemic-hypoxic conditions by inhibiting autophagy through ERK signaling pathway activation. These findings provide a theoretical foundation for the use of TFP in treating lower limb ischemia and highlight its potential to improve treatment protocols and outcomes.

人胎盘源性间充质干细胞(HP-MSCs)因其多向分化和免疫调节能力而被公认为具有治疗多种疾病的潜力。然而,在缺血和缺氧环境下,治疗效果往往受到损害。银耳银耳多糖(TFP)是一种天然多糖,以其免疫调节和抗炎特性而闻名,很有可能克服这一限制。我们的研究探讨了TFP是否通过抑制自噬来增强HP-MSCs在缺血-缺氧条件下的治疗效果,并重点研究了ERK信号通路的作用。在缺氧条件下模拟缺血环境培养HP-MSCs,加入TFP观察其对MSC生物活性、细胞凋亡和增殖的影响。我们进行了机制研究,以评估ERK信号通路的激活和自噬相关标志物的表达。TFP通过减少细胞凋亡和促进细胞增殖来增强HP-MSC在缺氧条件下的生物活性。机制分析显示,TFP通过激活ERK信号通路增强HP-MSCs适应低氧应激的能力。这种激活导致自噬相关标记物的抑制,表明TFP在缺氧诱导的细胞应激中起保护作用。TFP通过激活ERK信号通路抑制自噬,从而增强HP-MSCs在缺血-缺氧条件下的治疗潜力。这些发现为使用TFP治疗下肢缺血提供了理论基础,并强调了其改善治疗方案和结果的潜力。
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来源期刊
European Journal of Translational Myology
European Journal of Translational Myology MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
3.30
自引率
27.30%
发文量
74
审稿时长
10 weeks
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