Cargando…
A comparison of the bone and growth phenotype of mdx, mdx:Cmah(−/−) and mdx:Utrn(+/−) murine models with the C57BL/10 wild-type mouse
The muscular dystrophy X-linked (mdx) mouse is commonly used as a mouse model of Duchenne muscular dystrophy (DMD). Its phenotype is, however, mild, and other mouse models have been explored. The mdx:Cmah(−/−) mouse carries a human-like mutation in the Cmah gene and has a severe muscle phenotype, bu...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6994935/ https://www.ncbi.nlm.nih.gov/pubmed/31754018 http://dx.doi.org/10.1242/dmm.040659 |
Sumario: | The muscular dystrophy X-linked (mdx) mouse is commonly used as a mouse model of Duchenne muscular dystrophy (DMD). Its phenotype is, however, mild, and other mouse models have been explored. The mdx:Cmah(−/−) mouse carries a human-like mutation in the Cmah gene and has a severe muscle phenotype, but its growth and bone development are unknown. In this study, we compared male mdx, mdx:Utrn(+/−), mdx:Cmah(−/−) and wild-type (WT) mice at 3, 5 and 7 weeks of age to determine the suitability of the mdx:Cmah(−/−) mouse as a model for assessing growth and skeletal development in DMD. The mdx:Cmah(−/−) mice were lighter than WT mice at 3 weeks, but heavier at 7 weeks, and showed an increased growth rate at 5 weeks. Cortical bone fraction as assessed by micro-computed tomography was greater in both mdx and mdx:Cmah(−/−) mice versus WT mice at 7 weeks. Tissue mineral density was also higher in mdx:Cmah(−/−) mice at 3 and 7 weeks. Gene profiling of mdx:Cmah(−/−) bone identified increased expression of Igf1, Igf1r and Vegfa. Both the mdx and mdx:Cmah(−/−) mice showed an increased proportion of regulated bone marrow adipose tissue (BMAT) but a reduction in constitutive BMAT. The mdx:Cmah(−/−) mice show evidence of catch-up growth and more rapid bone development. This pattern does not mimic the typical DMD growth trajectory and therefore the utility of the mdx:Cmah(−/−) mouse for studying growth and skeletal development in DMD is limited. Further studies of this model may, however, shed light on the phenomenon of catch-up growth. This article has an associated First Person interview with the first author of the paper. |
---|