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对mdx小鼠再生肌肉中肌源性调节因子表达的原位杂交分析。

In situ hybridization analysis for expression of myogenic regulatory factors in regenerating muscle of mdx mouse.

作者信息

Bhagavati S, Ghatpande A, Shafiq S A, Leung B

机构信息

State University of New York Health Sciences Center, Department of Neurology, Brooklyn 11203, USA.

出版信息

J Neuropathol Exp Neurol. 1996 May;55(5):509-14. doi: 10.1097/00005072-199605000-00002.

Abstract

Precise temporal and spatial coordination of expression of the myogenic regulatory factors (MRF) plays a critical role in the development of skeletal muscle. Whether this pattern is recapitulated postnatally during regeneration of mature muscle after injury is not known. The aim of this study was to determine the cellular distribution of mRNA expression of the various myogenic regulatory factors (MyoD, Myogenin, Myf-5 and Myf-6) during regeneration in mature skeletal muscle. We used the mdx mouse, an animal model for Duchenne muscular dystrophy, which undergoes necrosis and vigorous regeneration of muscle fibers, as a natural model to study muscle fibers at various stages of maturity ranging from satellite cells to mature muscle fibers. In situ hybridization analysis revealed that MyoD expression was the most widespread and was expressed in satellite cells and small regenerating muscle fibers surrounding necrotic fibers. Myogenin, Myf5, and Myf6 were expressed weakly in some immature fibers and none of the MRF's could be detected in mature muscle. These findings, taken together with previous studies, suggests that the pattern of expression of the various MRF's in regenerating skeletal muscle differs from that in developing muscle in embryos and that MyoD may play a critical role in the initiation and progression of events which lead to regeneration in mature skeletal muscle.

摘要

生肌调节因子(MRF)表达精确的时空协调在骨骼肌发育中起着关键作用。损伤后成熟肌肉再生过程中是否重现这种模式尚不清楚。本研究的目的是确定成熟骨骼肌再生过程中各种生肌调节因子(MyoD、肌细胞生成素、Myf-5和Myf-6)mRNA表达的细胞分布。我们使用mdx小鼠,一种杜氏肌营养不良症的动物模型,其经历肌纤维坏死和强力再生,作为研究从卫星细胞到成熟肌纤维不同成熟阶段肌纤维的天然模型。原位杂交分析显示,MyoD表达最为广泛,在卫星细胞和围绕坏死纤维的小再生肌纤维中表达。肌细胞生成素、Myf5和Myf6在一些未成熟纤维中弱表达,在成熟肌肉中未检测到任何一种MRF。这些发现与先前的研究一起表明,再生骨骼肌中各种MRF的表达模式与胚胎发育肌肉中的不同,并且MyoD可能在导致成熟骨骼肌再生的事件的起始和进展中起关键作用。

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