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小鼠遗传性运动终板病(med):对解离的肌原细胞及其在培养中的发育的观察。

Hereditary motor endplate disease (med) of the mouse: observations on dissociated myogenic cells and their development in culture.

作者信息

Jockusch H, Burkart W, Burger M M

出版信息

Cell Tissue Res. 1980;207(2):241-8. doi: 10.1007/BF00237809.

Abstract

Myogenic cells from mice homozygous for the lethal mutation "motor endplate disease" (med/med) were grown in culture. Like muscle cells taken from wild type (+/?) litter mates they fused to form myotubes which contracted, developed cross striations, and exposed acetylcholine receptors (AChR) on their surface. However, a decrease of 30% in the number of mononucleated cells per unit fresh weight of muscle was observed as early as 2--3 days postnatal, i.e., at least one week prior to the onset of physiological symptoms. Hence, in addition to influencing the functional maintenance of motor endplates, the med gene seems to control early events in muscle development.

摘要

对致死性突变“运动终板疾病”(med/med)纯合的小鼠的生肌细胞在培养中生长。与取自野生型(+/?)同窝仔畜的肌肉细胞一样,它们融合形成肌管,这些肌管会收缩、出现横纹,并在其表面暴露乙酰胆碱受体(AChR)。然而,早在出生后2至3天,即生理症状出现前至少一周,就观察到每单位肌肉鲜重的单核细胞数量减少了30%。因此,除了影响运动终板的功能维持外,med基因似乎还控制着肌肉发育的早期事件。

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