Institute of Cellular and Organismic Biology, Academia Sinica, Taipei 115, Taiwan.
Sci Rep. 2013;3:1176. doi: 10.1038/srep01176. Epub 2013 Jan 31.
Myogenic progenitor cell (MPC) is responsible for postembryonic muscle growth and regeneration. Progranulin (PGRN) is a pluripotent growth factor that is correlated with neuromuscular disease, which is characterised by denervation, leading to muscle atrophy with an abnormal quantity and functional ability of MPC. However, the role of PGRN in MPC biology has yet to be elucidated. Here, we show that knockdown of zebrafish progranulin A (GrnA) resulted in a reduced number of MPC and impaired muscle growth. The decreased number of Pax7-positive MPCs could be restored by the ectopic expression of GrnA or MET. We further confirmed the requirement of GrnA in MPC activation during muscle regeneration by knockdown and transgenic line with muscle-specific overexpression of GrnA. In conclusion, we demonstrate a critical role for PGRN in the maintenance of MPC and suggest that muscle atrophy under PGRN loss may begin with MPC during postembryonic myogenesis.
成肌祖细胞(MPC)是胚胎后肌肉生长和再生的关键。颗粒蛋白前体(PGRN)是一种多能生长因子,与神经肌肉疾病相关,其特征为去神经支配,导致 MPC 的数量和功能异常,从而发生肌肉萎缩。然而,PGRN 在 MPC 生物学中的作用仍有待阐明。在这里,我们发现敲低斑马鱼颗粒蛋白前体 A(GrnA)导致 MPC 数量减少和肌肉生长受损。通过异位表达 GrnA 或 MET 可恢复减少的 Pax7 阳性 MPC 数量。我们进一步通过肌肉特异性过表达 GrnA 的敲低和转基因系证实了 GrnA 在肌肉再生过程中对 MPC 激活的必要性。总之,我们证明了 PGRN 在维持 MPC 中的关键作用,并表明 PGRN 缺失导致的肌肉萎缩可能始于胚胎后肌发生过程中的 MPC。