首页> 外文期刊>Brazilian Journal of Medical and Biological Research >Implantation of muscle satellite cells overexpressing myogenin improves denervated muscle atrophy in rats
【24h】

Implantation of muscle satellite cells overexpressing myogenin improves denervated muscle atrophy in rats

机译:植入过度表达肌生成素的肌肉卫星细胞可改善大鼠失神经支配的肌肉萎缩

获取原文
       

摘要

This study evaluated the effect of muscle satellite cells (MSCs) overexpressing myogenin (MyoG) on denervated muscle atrophy. Rat MSCs were isolated and transfected with the MyoG-EGFP plasmid vector GV143. MyoG-transfected MSCs (MTMs) were transplanted into rat gastrocnemius muscles at 1 week after surgical denervation. Controls included injections of untransfected MSCs or the vehicle only. Muscles were harvested and analyzed at 2, 4, and 24 weeks post-transplantation. Immunofluorescence confirmed MyoG overexpression in MTMs. The muscle wet weight ratio was significantly reduced at 2 weeks after MTM injection (67.17?±6.79) compared with muscles injected with MSCs (58.83?±5.31) or the vehicle (53.00?±7.67; t=2.37, P=0.04 and t=3.39, P=0.007, respectively). The muscle fiber cross-sectional area was also larger at 2 weeks after MTM injection (2.63??10 3 ?±0.39??10 3 ) compared with MSC injection (1.99??10 3 ?±0.58??10 3 ) or the vehicle only (1.57??10 3 ?±0.47??10 3 ; t=2.24, P=0.049 and t=4.22, P=0.002, respectively). At 4 and 24 weeks post-injection, the muscle mass and fiber cross-sectional area were similar across all three experimental groups. Immunohistochemistry showed that the MTM group had larger MyoG-positive fibers. The MTM group (3.18?±1.13) also had higher expression of MyoG mRNA than other groups (1.41?±0.65 and 1.03?±0.19) at 2 weeks after injection (t=2.72, P=0.04). Transplanted MTMs delayed short-term atrophy of denervated muscles. This approach can be optimized as a novel stand-alone therapy or as a bridge to surgical re-innervation of damaged muscles.
机译:这项研究评估了过度表达肌原蛋白(MyoG)的肌肉卫星细胞(MSCs)对失神经的肌肉萎缩的影响。分离大鼠MSC并用MyoG-EGFP质粒载体GV143转染。手术神经支配后1周,将MyoG转染的MSC(MTM)移植到大鼠腓肠肌中。对照包括未转染的MSC或仅注射载体。移植后第2、4和24周收获肌肉并进行分析。免疫荧光证实了MTM中MyoG的过度表达。与注射MSCs(58.83?±5.31)或媒介物(53.00?±7.67; t = 2.37,P = 0.04和t)相比,注射MTM后2周的肌肉湿重比显着降低(67.17?±6.79)。 = 3.39,P = 0.007)。 MMSC注射后2周的肌纤维横截面积也较大(2.63?10 3?±0.39?10 3),而MSC注射(1.99?10 3 3±±0.58?10 3)或更大。仅车辆(1.57≤103≤±0.47≤103; t = 2.24,P = 0.049和t = 4.22,P = 0.002)。注射后4周和24周,所有三个实验组的肌肉质量和纤维横截面积均相似。免疫组织化学显示,MTM组具有较大的MyoG阳性纤维。注射后2周,MTM组(3.18≤±1.13)也比其他组(1.41≤±0.65和1.03≤±0.19)具有更高的MyoG mRNA表达(t = 2.72,P = 0.04)。移植的MTM延迟了神经支配的肌肉的短期萎缩。可以将这种方法优化为一种新颖的独立治疗方法,或作为对受损肌肉进行手术神经支配的桥梁。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号