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Skeletal Muscle Fibrosis in the mdx/utrn+/- Mouse Validates Its Suitability as a Murine Model of Duchenne Muscular Dystrophy

机译:mdx / utrn +/-小鼠的骨骼肌纤维化验证了其作为Duchenne肌营养不良的小鼠模型的适用性

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摘要

Various therapeutic approaches have been studied for the treatment of Duchenne muscular dystrophy (DMD), but none of these approaches have led to significant long-term effects in patients. One reason for this observed inefficacy may be the use of inappropriate animal models for the testing of therapeutic agents. The mdx mouse is the most widely used murine model of DMD, yet it does not model the fibrotic progression observed in patients. Other murine models of DMD are available that lack one or both alleles of utrophin, a functional analog of dystrophin. The aim of this study was to compare fibrosis and myofiber damage in the mdx, mdx/utrn+/- and double knockout (dko) mouse models. We used Masson’s trichrome stain and percentage of centrally-nucleated myofibers as indicators of fibrosis and myofiber regeneration, respectively, to assess disease progression in diaphragm and gastrocnemius muscles harvested from young and aged wild-type, mdx, mdx/utrn+/- and dko mice. Our results indicated that eight week-old gastrocnemius muscles of both mdx/utrn+/- and dko hind limb developed fibrosis whereas age-matched mdx gastrocnemius muscle did not (p = 0.002). The amount of collagen found in the mdx/utrn+/- diaphragm was significantly higher than that found in the corresponding diaphragm muscles of wild-type animals, but not of mdx animals (p = 0.0003). Aged mdx/utrn+/- mice developed fibrosis in both diaphragm and gastrocnemius muscles compared to wild-type controls (p = 0.003). Mdx diaphragm was fibrotic in aged mice as well (p = 0.0235), whereas the gastrocnemius muscle in these animals was not fibrotic. We did not measure a significant difference in collagen staining between wild-type and mdx gastrocnemius muscles. The results of this study support previous reports that the moderately-affected mdx/utrn+/- mouse is a better model of DMD, and we show here that this difference is apparent by 2 months of age.
机译:已经研究了多种治疗方法来治疗杜氏肌营养不良症(DMD),但这些方法均未对患者产生明显的长期影响。观察到这种无效的原因之一可能是使用不合适的动物模型来测试治疗剂。 mdx小鼠是使用最广泛的DMD小鼠模型,但不能模拟患者中观察到的纤维化进程。还可以使用缺少Utrophin(抗肌萎缩蛋白的功能类似物)的一个或两个等位基因的DMD的其他鼠模型。这项研究的目的是比较mdx,mdx / utrn +/-和双敲除(dko)小鼠模型中的纤维化和肌纤维损伤。我们分别使用Masson的三色染色和中央成核肌纤维的百分比作为纤维化和肌纤维再生的指标,以评估从年轻人和老年野生型,mdx,mdx / utrn +/-和dko小鼠收获的diaphragm肌和腓肠肌的疾病进展。我们的研究结果表明,mdx / utrn +/-和dko后肢的八周大腓肠肌均发生纤维化,而年龄匹配的mdx腓肠肌则无纤维化(p = 0.002)。在mdx / utrn +/- diaphragm肌中发现的胶原蛋白含量明显高于野生型动物的相应diaphragm肌中发现的胶原蛋白含量,但在mdx动物中则没有(p = 0.0003)。与野生型对照组相比,老年mdx / utrn +/-小鼠的diaphragm肌和腓肠肌均出现纤维化(p = 0.003)。 Mdx diaphragm肌在老年小鼠中也有纤维化(p = 0.0235),而这些动物的腓肠肌也没有纤维化。我们没有测量野生型和mdx腓肠肌之间胶原蛋白染色的显着差异。这项研究的结果支持以前的报道,即中度受影响的mdx / utrn +/-小鼠是DMD的更好模型,我们在这里表明,这种差异在2个月大时就很明显。

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