Neurosciences Division - Human Genetics, CHUQ Research Center - CHUL, Quebec, QC, Canada.
Neuromuscul Disord. 2013 Feb;23(2):155-9. doi: 10.1016/j.nmd.2012.10.020. Epub 2012 Nov 30.
A rhesus macaque with generalized muscle atrophy and musculotendinous contractures was detected in our research center. Muscle biopsies showed myofibers with rimmed vacuoles and eosinophilic hyaline inclusions, accumulations of CD8+ and CD4+ lymphocytes and expression of major histocompatibility complex class I in myofibers. Intracellular inclusions were positive to Congo red. Semithin sections and transmission electron microscopy showed autophagic vacuoles within myofibers and myonuclei with inclusions of filaments. These morphological observations conform with the diagnostic criteria of human sporadic inclusion body myositis. This is the first report of this myopathy in nonhuman primates.
在我们的研究中心发现了一只患有全身性肌肉萎缩和肌肉腱挛缩的恒河猴。肌肉活检显示肌纤维有镶边空泡和嗜酸性透明包涵体,CD8+和 CD4+淋巴细胞聚集,以及肌纤维中主要组织相容性复合体 I 的表达。细胞内包涵体对刚果红呈阳性。半薄切片和透射电子显微镜显示肌纤维内自噬空泡和含丝状体的肌细胞核内包涵体。这些形态学观察符合人类散发性包涵体肌病的诊断标准。这是首例在非人类灵长类动物中发现的这种肌病。