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mdx肌肉移植在正常宿主中保留mdx表型。

Mdx muscle grafts retain the mdx phenotype in normal hosts.

作者信息

Morgan J E, Coulton G R, Partridge T A

机构信息

Department of Histopathology, Charing Cross and Westminster Medical School, London, UK.

出版信息

Muscle Nerve. 1989 May;12(5):401-9. doi: 10.1002/mus.880120511.

Abstract

Whole muscle grafts were made between mdx and normal mice to investigate whether the mdx myopathic lesion is intrinsic to mdx muscle or is a property of its environment. Grafts were examined between 20 and 101 days. Unequivocal necrotic muscle fibers and/or newly formed basophilic myotubes were noted in 8 of 16 grafts of mdx muscle made in normal hosts but in none of 16 grafts of normal muscle made in mdx hosts. In older grafts, the proportion of centrally nucleated fibers and variability of fiber diameter were both higher in mdx muscle grafted into normal hosts than in normal muscle grafted into either mdx or normal hosts. Analysis of the glucose-6-phosphate isomerase (GPI) isoenzyme content of the grafts indicated that the muscle formed was predominantly of donor origin. These findings provide evidence that the mdx lesion is a primary myopathy rather than secondary to an extramuscular primary lesion.

摘要

将mdx小鼠和正常小鼠之间进行全肌移植,以研究mdx肌病性病变是mdx肌肉固有的,还是其环境的一种特性。在20至101天之间检查移植组织。在正常宿主中制作的16个mdx肌肉移植组织中,有8个发现了明确的坏死肌纤维和/或新形成的嗜碱性肌管,但在mdx宿主中制作的16个正常肌肉移植组织中均未发现。在较老的移植组织中,移植到正常宿主的mdx肌肉中,中央核纤维的比例和纤维直径的变异性均高于移植到mdx或正常宿主的正常肌肉。对移植组织的葡萄糖-6-磷酸异构酶(GPI)同工酶含量分析表明,形成的肌肉主要来自供体。这些发现提供了证据,证明mdx病变是原发性肌病,而非继发于肌肉外原发性病变。

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