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抑制核因子κB可改善从自然衰老小鼠分离出的间充质干细胞的应激抗性和成肌分化。

Inhibition of NF-κB improves the stress resistance and myogenic differentiation of MDSPCs isolated from naturally aged mice.

作者信息

Proto Jonathan D, Lu Aiping, Dorronsoro Akaitz, Scibetta Alex, Robbins Paul D, Niedernhofer Laura J, Huard Johnny

机构信息

Department of Medicine, Division of Molecular Medicine, Columbia University, New York, NY, United States of America.

Department of Orthopaedic Surgery, Institute of Molecular Medicine, University of Texas Health Science Center at Houston, McGovern Medical School, Houston, TX, United States of America.

出版信息

PLoS One. 2017 Jun 22;12(6):e0179270. doi: 10.1371/journal.pone.0179270. eCollection 2017.

Abstract

A decline in the regenerative capacity of adult stem cells with aging is well documented. As a result of this decline, the efficacy of autologous stem cell therapies is likely to decline with increasing donor age. In these cases, strategies to restore the function of aged stem cells would have clinical utility. Globally, the transcription factor NF-κB is up-regulated in aged tissues. Given the negative role that NF-κB plays in myogenesis, we investigated whether the age-related decline in the function of muscle-derived stem/progenitor cells (MDSPCs) could be improved by inhibition of NF-κB. Herein, we demonstrate that pharmacologic or genetic inhibition of NF-κB activation increases myogenic differentiation and improves resistance to oxidative stress. Our results suggest that MDSPC "aging" may be reversible, and that pharmacologic targeting of pathways such as NF-κB may enhance the efficacy of cell-based therapies.

摘要

成年干细胞的再生能力随衰老而下降,这一点已有充分记录。由于这种下降,自体干细胞疗法的疗效可能会随着供体年龄的增加而下降。在这些情况下,恢复衰老干细胞功能的策略将具有临床应用价值。在全球范围内,转录因子NF-κB在衰老组织中上调。鉴于NF-κB在肌生成中发挥的负面作用,我们研究了通过抑制NF-κB是否可以改善与年龄相关的肌肉来源的干/祖细胞(MDSPCs)功能下降。在此,我们证明,对NF-κB激活的药物或基因抑制可增加肌源性分化并提高对氧化应激的抵抗力。我们的结果表明,MDSPC的“衰老”可能是可逆的,并且对NF-κB等通路的药物靶向治疗可能会提高基于细胞的疗法的疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00ed/5480862/86c55654984d/pone.0179270.g001.jpg

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