Mito Takayuki, Ishizaki Hikari, Suzuki Michiko, Morishima Hitomi, Ota Azusa, Ishikawa Kaori, Nakada Kazuto, Maeno Akiteru, Shiroishi Toshihiko, Hayashi Jun-Ichi
Faculty of Life and Environmental Sciences, University of Tsukuba, Tsukuba, Ibaraki, Japan.
Faculty of Life and Environmental Sciences, University of Tsukuba, Tsukuba, Ibaraki, Japan; International Institute for Integrative Sleep Medicine (WPI-IIIS), University of Tsukuba, Tsukuba, Ibaraki, Japan.
Biochem Biophys Res Commun. 2015 Jan 24;456(4):933-7. doi: 10.1016/j.bbrc.2014.12.009. Epub 2014 Dec 12.
The spectra of phenotypes associated with aging and mitochondrial diseases sometimes appear to overlap with each other. We used aged mice and a mouse model of mitochondrial diseases (transmitochondrial mito-miceΔ with deleted mtDNA) to study whether premature aging phenotypes observed in mtDNA mutator mice are associated with aging or mitochondrial diseases. Here, we provide convincing evidence that all the mice examined had musculoskeletal disorders of osteoporosis and muscle atrophy, which correspond to phenotypes prevalently observed in the elderly. However, precise investigation of musculoskeletal disorders revealed that the spectra of osteoporosis and muscle atrophy phenotypes in mtDNA mutator mice were very close to those in mito-miceΔ, but different from those of aged mice. Therefore, mtDNA mutator mice and mito-miceΔ, but not aged mice, share the spectra of musculoskeletal disorders.
与衰老和线粒体疾病相关的表型谱有时似乎相互重叠。我们使用老年小鼠和线粒体疾病小鼠模型(线粒体DNA缺失的转线粒体mito - miceΔ)来研究在mtDNA突变小鼠中观察到的早衰表型是与衰老还是线粒体疾病相关。在这里,我们提供了令人信服的证据,即所有检查的小鼠都患有骨质疏松症和肌肉萎缩的肌肉骨骼疾病,这与在老年人中普遍观察到的表型相对应。然而,对肌肉骨骼疾病的精确研究表明,mtDNA突变小鼠中骨质疏松症和肌肉萎缩表型谱与mito - miceΔ非常接近,但与老年小鼠不同。因此,mtDNA突变小鼠和mito - miceΔ,而不是老年小鼠,共享肌肉骨骼疾病谱。