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Myogenic differentiation potential of human tonsil-derived mesenchymal stem cells and their potential for use to promote skeletal muscle regeneration

机译:人扁桃体间充质干细胞的成肌分化潜能及其用于促进骨骼肌再生的潜能

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Stem cells are regarded as an important source of cells which may be used to promote the regeneration of skeletal muscle (SKM) which has been damaged due to defects in the organization of muscle tissue caused by congenital diseases, trauma or tumor removal. In particular, mesenchymal stem cells (MSCs), which require less invasive harvesting techniques, represent a valuable source of cells for stem cell therapy. In the present study, we demonstrated that human tonsil-derived MSCs (T-MSCs) may differentiate into myogenic cells in vitro and that the transplantation of myoblasts and myocytes generated from human T-MSCs mediates the recovery of muscle function in vivo. In order to induce myogenic differentiation, the T-MSC-derived spheres were cultured in Dulbecco's modified Eagle's mediumutrient mixture F-12 (DMEM/F-12) supplemented with 1 ng/ml transforming growth factor-, non-essential amino acids and insulin-transferrin-selenium for 4 days followed by culture in myogenic induction medium [low-glucose DMEM containing 2% fetal bovine serum (FBS) and 10 ng/ml insulin-like growth factor 1 (IGF1)] for 14 days. The T-MSCs sequentially differentiated into myoblasts and skeletal myocytes, as evidenced by the increased expression of skeletal myogenesis-related markers [including -actinin, troponin I type 1 (TNNI1) and myogenin] and the formation of myotubes in vitro. The in situ transplantation of T-MSCs into mice with a partial myectomy of the right gastrocnemius muscle enhanced muscle function, as demonstrated by gait assessment (footprint analysis), and restored the shape of SKM without forming teratomas. Thus, T-MSCs may differentiate into myogenic cells and effectively regenerate SKM following injury. These results demonstrate the therapeutic potential of T-MSCs to promote SKM regeneration following injury.
机译:干细胞被认为是细胞的重要来源,可用于促进骨骼肌(SKM)的再生,该骨骼肌由于先天性疾病,创伤或肿瘤切除引起的肌肉组织组织缺陷而受损。特别是,需要较少侵入性收获技术的间充质干细胞(MSC)代表了干细胞治疗的宝贵细胞来源。在本研究中,我们证明了人类扁桃体来源的MSC(T-MSC)可能在体外分化为成肌细胞,并且人T-MSC生成的成肌细胞和心肌细胞的移植介导了体内肌肉功能的恢复。为了诱导肌原性分化,将T-MSC衍生的球体在Dulbecco改良的Eagle培养基/营养混合物F-12(DMEM / F-12)中培养,该混合物中添加了1 ng / ml的转化生长因子-非必需氨基酸胰岛素和转铁蛋白硒治疗4天,然后在成肌诱导培养基[含有2%胎牛血清(FBS)和10 ng / ml胰岛素样生长因子1(IGF1)的低葡萄糖DMEM]中培养14天。 T-MSCs依次分化为成肌细胞和骨骼肌细胞,这由骨骼肌发生相关标志物(包括肌动蛋白,肌钙蛋白I 1型(TNNI1)和肌生成素)的表达增加以及体外肌管形成所证明。如步态评估(足迹分析)所证实,将T-MSCs原位移植到小鼠右侧腓肠肌部分肌切除术中可增强肌肉功能,并恢复了SKM的形状而未形成畸胎瘤。因此,T-MSCs可能分化为成肌细胞,并在损伤后有效地再生SKM。这些结果证明了T-MSC在损伤后促进SKM再生的治疗潜力。

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