Department of Physiology, Universidad de Sevilla, 41012 Seville, Spain.
Cells. 2020 Mar 18;9(3):747. doi: 10.3390/cells9030747.
Extraocular muscles (EOMs) show resistance to muscle dystrophies and sarcopenia. It has been recently demonstrated that they are endowed with different types of myogenic cells, all of which present an outstanding regenerative potential. Neurotrophins are important modulators of myogenic regeneration and act promoting myoblast proliferation, enhancing myogenic fusion rates and protecting myotubes from inflammatory stimuli. Here, we adapted the pre-plate cell isolation technique to obtain myogenic progenitors from the rat EOMs, and quantified their in vitro expression of neurotrophins and their receptors by RT-qPCR and immunohistochemistry, respectively. The results were compared with the expression on progenitors isolated from buccinator, tongue and limb muscles. Our quantitative analysis of brain-derived neurotrophic factor (BDNF), nerve growth factor (NGF) and neurotrophin-3 (NT-3) transcripts showed, for the first time, that EOMs-derived cells express more of these factors and that they expressed TrkA, but not TrkB and TrkC receptors. On the contrary, the immunofluorescence analysis demonstrated high expression of p75 on all myogenic progenitors, with the EOMs-derived cells showing higher expression. Taken together, these results suggest that the intrinsic trophic differences between EOMs-derived myogenic progenitors and their counterparts from other muscles could explain why those cells show higher proliferative and fusion rates, as well as better regenerative properties.
眼外肌 (EOM) 对肌肉营养不良和肌肉减少症具有抗性。最近有研究表明,它们具有不同类型的成肌细胞,所有这些细胞都具有出色的再生潜力。神经营养因子是成肌再生的重要调节剂,可促进成肌细胞增殖,提高成肌融合率,并保护肌管免受炎症刺激。在这里,我们采用预培养细胞分离技术从大鼠 EOM 中获得成肌祖细胞,并通过 RT-qPCR 和免疫组织化学分别定量分析它们的神经营养因子及其受体的表达。结果与从颊肌、舌肌和四肢肌肉分离的祖细胞的表达进行了比较。我们对脑源性神经营养因子 (BDNF)、神经生长因子 (NGF) 和神经生长因子-3 (NT-3) 转录本的定量分析首次表明,EOM 衍生细胞表达更多的这些因子,并且它们表达 TrkA,但不表达 TrkB 和 TrkC 受体。相反,免疫荧光分析表明,所有成肌祖细胞均高表达 p75,EOM 衍生细胞的表达更高。综上所述,这些结果表明,EOM 衍生的成肌祖细胞与其他肌肉来源的成肌祖细胞之间的内在营养差异可以解释为什么这些细胞具有更高的增殖和融合率以及更好的再生特性。