Pichavant Christophe, Gargioli Cesare, Tremblay Jacques P
Department of Pharmacology, Emory University, Atlanta, Georgia, USA; Department of Biology University of RomeTor Vergata, Italy and Professor, Department of Human Genetics, CHUL Research Center, Quebec City, Canada.
PLoS Curr. 2011 Oct 26;3:RRN1275. doi: 10.1371/currents.RRN1275.
Duchenne muscular dystrophy (DMD) is characterized by the absence of dystrophin in muscles. A therapeutic approach to restore dystrophin expression in DMD patient's muscles is the transplantation of muscle precursor cells (MPCs). However, this transplantation is limited by the low MPC capacity to migrate beyond the injection trajectory. Matrix metalloproteases (MMPs) are key regulatory molecules in the remodeling of extracellular matrix (ECM) components. MPCs over-expressing MMP-9 were tested by zymography, migration and invasion assays in vitro and by transplantation in mouse muscle. In vitro, MPCs over-expressing MMP-9 have a better invasion capacity than control MPCs. When these cells are transplanted in mouse muscles, the transplantation success is increased by more than 50% and their dispersion is higher than normal cells. MMP-9 over-expression could thus be an approach to improve cell transplantation in DMD patients by increasing the dispersion capacity of transplanted cells.
杜氏肌营养不良症(DMD)的特征是肌肉中缺乏抗肌萎缩蛋白。恢复DMD患者肌肉中抗肌萎缩蛋白表达的一种治疗方法是移植肌肉前体细胞(MPCs)。然而,这种移植受到MPCs迁移能力低的限制,它们难以迁移到注射轨迹之外。基质金属蛋白酶(MMPs)是细胞外基质(ECM)成分重塑中的关键调节分子。通过体外酶谱分析、迁移和侵袭试验以及在小鼠肌肉中的移植,对过表达MMP-9的MPCs进行了测试。在体外,过表达MMP-9的MPCs比对照MPCs具有更好的侵袭能力。当将这些细胞移植到小鼠肌肉中时,移植成功率提高了50%以上,并且它们的扩散程度高于正常细胞。因此,过表达MMP-9可能是一种通过提高移植细胞的扩散能力来改善DMD患者细胞移植的方法。