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胰岛素通过激活Akt-细胞周期蛋白D1轴促进人脐带基质间充质干细胞的增殖。

Insulin Promotes the Proliferation of Human Umbilical Cord Matrix-Derived Mesenchymal Stem Cells by Activating the Akt-Cyclin D1 Axis.

作者信息

Li Peng, Wei Jinsong, Gao Xiang, Wei Bo, Lin Hao, Huang Rui, Niu Yanru, Lim Kyu, Jing Kaipeng, Chu Jiaqi

机构信息

Stem Cell Research and Cellular Therapy Center, Affiliated Hospital of Guangdong Medical University, Zhanjiang, China.

Department of Spinal Surgery, Affiliated Hospital of Guangdong Medical University, Zhanjiang, China.

出版信息

Stem Cells Int. 2017;2017:7371615. doi: 10.1155/2017/7371615. Epub 2017 Apr 18.

Abstract

. The functions of insulin in mesenchymal stem cells (MSC) remain poorly understood. MSC from human umbilical cord matrix (UCM) cultured in serum-free media (SFM) with or without insulin were subjected to various molecular biological analyses to determine their proliferation and growth states, expression levels of Akt-cyclin D1 signaling molecules, and in vitro differentiation capacities. Insulin accelerated the G1-S cell cycle progression of UCM-MSC and significantly stimulated their proliferation and growth in SFM. The pro-proliferative action of insulin was associated with augmented cyclin D1 and phosphorylated Akt expression levels. Akt inactivation remarkably abrogated insulin-induced increases in cyclin D1 expression and cell proliferation, indicating that insulin enhances the proliferation of UCM-MSC via acceleration of the G1-S transition mediated by the Akt-cyclin D1 pathway. Additionally, the UCM-MSC propagated in SFM supplemented with insulin exhibited similar specific surface antigen profiles and differentiation capacities as those generated in conventional media containing fetal bovine serum. These findings suggest that insulin acts solely to promote UCM-MSC proliferation without affecting their immunophenotype and differentiation potentials and thus have important implications for utilizing insulin to expand clinical-grade MSC in vitro.

摘要

胰岛素在间充质干细胞(MSC)中的功能仍未得到充分了解。将来自人脐带基质(UCM)的MSC在含或不含胰岛素的无血清培养基(SFM)中培养,然后进行各种分子生物学分析,以确定其增殖和生长状态、Akt-细胞周期蛋白D1信号分子的表达水平以及体外分化能力。胰岛素加速了UCM-MSC的G1-S细胞周期进程,并显著刺激了它们在SFM中的增殖和生长。胰岛素的促增殖作用与细胞周期蛋白D1和磷酸化Akt表达水平的增加有关。Akt失活显著消除了胰岛素诱导的细胞周期蛋白D1表达增加和细胞增殖,表明胰岛素通过加速由Akt-细胞周期蛋白D1途径介导的G1-S转变来增强UCM-MSC的增殖。此外,在补充胰岛素的SFM中增殖的UCM-MSC表现出与在含有胎牛血清的传统培养基中产生的细胞相似的特异性表面抗原谱和分化能力。这些发现表明,胰岛素仅起到促进UCM-MSC增殖的作用,而不影响其免疫表型和分化潜能,因此对利用胰岛素在体外扩增临床级MSC具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d2f/5412176/7dee7f32a546/SCI2017-7371615.001.jpg

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