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抗坏血酸通过调节椎间盘退变过程中的增殖来促进髓核细胞再生。

Ascorbic acid promotes nucleus pulposus cell regeneration by regulating proliferation during intervertebral disc degeneration.

作者信息

Yi Yu-Yang, Zhang Shu-Bao, Chen Hao, Xu Hao-Wei, Wang Shan-Jin

机构信息

Department of Spinal Surgery, Shanghai East Hospital, School of Medicine, Tongji University, Shanghai 200092, China.

Department of Spinal Surgery, Shanghai East Hospital, School of Medicine, Tongji University, Shanghai 200092, China; Department of orthopedic, East Hospital, Ji'an Hospital, Jinggangshan University School of Medicine, Jiangxi, China.

出版信息

J Nutr Biochem. 2022 Oct;108:109099. doi: 10.1016/j.jnutbio.2022.109099. Epub 2022 Jun 30.

Abstract

Intervertebral disc degeneration (IVDD) affects human health. Ascorbic acid (AA) deficiency is a major factor that contributes to the development of degenerative disc disease in the elderly. Here, as a novel treatment with promising applications, we demonstrate that AA treatment inhibited senescence and maintained the proliferation of nucleus pulposus (NP) cells during long-term culture. AA-treated NP cells and acupuncture-treated rat models exhibited degenerative resistance during cell passaging and AA increased cell proliferation and decreased time-related senescence. Interestingly, Kyoto Encyclopedia of Genes and Genomes pathway mapping revealed five top enriched pathways and four pathways were associated with the aldehyde dehydrogenase (ALDH) enzyme family, especially proliferation-related ALDH1A3. Collectively, our findings demonstrate that ALDH1A3 expression was increased by AA treatment, which counteracted degeneration in NP cells over time and rejuvenated maintenance of proliferation in NP cells, which has a promising therapeutic implications in IVDD.

摘要

椎间盘退变(IVDD)会影响人类健康。维生素C(AA)缺乏是导致老年人退行性椎间盘疾病发生的一个主要因素。在此,作为一种具有广阔应用前景的新型治疗方法,我们证明AA治疗可抑制衰老,并在长期培养过程中维持髓核(NP)细胞的增殖。经AA处理的NP细胞和经针刺治疗的大鼠模型在细胞传代过程中表现出抗退变能力,且AA可增加细胞增殖并减少与时间相关的衰老。有趣的是,京都基因与基因组百科全书通路映射显示了五个最富集的通路,其中四个通路与醛脱氢酶(ALDH)酶家族相关,尤其是与增殖相关的ALDH1A3。总体而言,我们的研究结果表明,AA处理可增加ALDH1A3的表达,这可随着时间的推移抵消NP细胞的退变,并使NP细胞增殖的维持恢复活力,这在IVDD中具有广阔的治疗前景。

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