Tomé F M, Askanas V, Engel W K, Alvarez R B, Lee C S
Groupe de Recherche de Biologie et Pathologie Neuromusculaire, INSERM U 153, Paris, France.
Neurology. 1989 Jul;39(7):926-32. doi: 10.1212/wnl.39.7.926.
We established monolayer muscle fiber cultures from muscle biopsies of 3 patients with oculopharyngeal muscular dystrophy (OPMD) who had characteristic intranuclear inclusions (INI-A) in their muscle fibers. Aneural cultures had normal morphology, except for a few muscle fibers that contained small vacuoles. Innervated cultures had large cytoplasmic vacuoles in a number of muscle fibers. Those muscle fibers were breaking easily, and could not be maintained longer than 2 months. Electron microscopy showed unusual intranuclear inclusions (INI-B) not previously reported in aneurally cultured muscle fibers of OPMD or in any normal or disease-control aneural or innervated cultured human muscle fibers. They resembled, but were not identical to, the INI-A, and they occurred in both the cultured fibers and the original muscle biopsies of all 3 patients. Our study demonstrate that (1) nuclear inclusions in OPMD reflect an intrinsic genetic defect; and (2) neuronal influence, advanced maturation, or both, seem to be essential for their induction in muscle fibers.
我们从3例眼咽型肌营养不良症(OPMD)患者的肌肉活检组织中建立了单层肌纤维培养物,这些患者的肌纤维中有特征性的核内包涵体(INI-A)。无神经支配的培养物形态正常,只是少数肌纤维含有小空泡。有神经支配的培养物中,许多肌纤维出现大的细胞质空泡。这些肌纤维很容易断裂,无法维持超过2个月。电子显微镜显示出异常的核内包涵体(INI-B),这在OPMD的无神经支配培养肌纤维中或任何正常或疾病对照的无神经支配或有神经支配的培养人肌纤维中均未见先前报道。它们与INI-A相似,但并不相同,并且出现在所有3例患者的培养纤维和原始肌肉活检组织中。我们的研究表明:(1)OPMD中的核内包涵体反映了一种内在的遗传缺陷;(2)神经元影响、晚期成熟或两者似乎对于它们在肌纤维中的诱导至关重要。