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间充质干/基质细胞调控中的活性氧、超氧化物歧化酶以及PTEN-p53-AKT-MDM2信号环路网络

Reactive Oxygen Species, Superoxide Dimutases, and PTEN-p53-AKT-MDM2 Signaling Loop Network in Mesenchymal Stem/Stromal Cells Regulation.

作者信息

Matsuda Satoru, Nakagawa Yukie, Kitagishi Yasuko, Nakanishi Atsuko, Murai Toshiyuki

机构信息

Department of Food Science and Nutrition, Nara Women's University, Kita-Uoya Nishimachi, Nara 630-8506, Japan.

Department of Food and Nutrition, Faculty of Contemporary Human Life Science, Tezukayama University, Nara 631-8501, Japan.

出版信息

Cells. 2018 May 1;7(5):36. doi: 10.3390/cells7050036.

Abstract

Mesenchymal stromal/stem cells (MSCs) are multipotent cells that can differentiate to various specialized cells, which have the potential capacity to differentiate properly and accelerate recovery in damaged sites of the body. This stem cell technology has become the fundamental element in regenerative medicine. As reactive oxygen species (ROS) have been reported to adversely influence stem cell properties, it is imperative to attenuate the extent of ROS to the promising protective approach with MSCs’ regenerative therapy. Oxidative stress also affects the culture expansion and longevity of MSCs. Therefore, there is great need to identify a method to prevent oxidative stress and replicative senescence in MSCs. Phosphatase and tensin homologue deleted on chromosome 10/Protein kinase B, PKB (PTEN/AKT) and the tumor suppressor p53 pathway have been proven to play a pivotal role in regulating cell apoptosis by regulating the oxidative stress and/or ROS quenching. In this review, we summarize the current research and our view of how PTEN/AKT and p53 with their partners transduce signals downstream, and what the implications are for MSCs’ biology.

摘要

间充质基质/干细胞(MSCs)是多能细胞,能够分化为各种特化细胞,具有在体内受损部位正常分化并加速恢复的潜在能力。这种干细胞技术已成为再生医学的基本要素。由于据报道活性氧(ROS)会对干细胞特性产生不利影响,因此将ROS的程度降低至MSCs再生治疗中具有前景的保护方法势在必行。氧化应激也会影响MSCs的培养扩增和寿命。因此,非常需要确定一种预防MSCs氧化应激和复制衰老的方法。10号染色体缺失的磷酸酶和张力蛋白同源物/蛋白激酶B,PKB(PTEN/AKT)以及肿瘤抑制因子p53途径已被证明在通过调节氧化应激和/或ROS淬灭来调节细胞凋亡中起关键作用。在这篇综述中,我们总结了当前的研究以及我们对于PTEN/AKT和p53与其伙伴如何向下游转导信号以及这对MSCs生物学有何影响的观点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c05/5981260/bf0b60c33db6/cells-07-00036-g001.jpg

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