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鱼精蛋白在体外诱导辣根过氧化物酶进入小鼠骨骼肌细胞内并引起空泡化。

Protamine induced intracellular uptake of horseradish peroxidase and vacuolation in mouse skeletal muscle in vitro.

作者信息

Jirmanová I, Libelius R, Lundquist I, Thesleff S

出版信息

Cell Tissue Res. 1977 Jan 24;176(4):463-73. doi: 10.1007/BF00231402.

Abstract

The uptake in vitro of horseradish peroxidase (HRP) in mouse skeletal muscle was examined by electron microscopy and chemical determination. In muscles exposed to an HRP solution for 60 min at +37 degrees C, HRP infiltrated the basal lamina of muscle fibres and caused an intense labelling of their sarcolemma. In addition HRP was found within the transverse tubules. Exposure to HRP for 30 min at +37 degrees C followed by HRP together with a polycationic protein (protamine) for 30 min at +37 degrees C caused an intracellular vesicular uptake of HRP. Intracellular HRP was found in numerous vesicles, membrane limited bodies and vacuoles. Protamine also induced focal autophagic vacuolation with progressive muscle fibre degeneration. An intracellular HRP uptake or muscle cell vacuolation could not be detected in the absence of protamine or when the incubation temperature was +4 degrees C. Chemical determination of HRP uptake was in general agreement with the morphological results. The uptake of HRP in the presence of protamine was stimulated at +37 degrees C and blocked at +4 degrees C. The results suggest that in skeletal muscle in vitro intracellular uptake of macromolecules occurs by endocytosis.

摘要

通过电子显微镜和化学测定法检测了辣根过氧化物酶(HRP)在小鼠骨骼肌中的体外摄取情况。在37℃下将肌肉暴露于HRP溶液60分钟,HRP渗入肌纤维的基膜并使其肌膜产生强烈标记。此外,在横管内也发现了HRP。在37℃下将肌肉暴露于HRP 30分钟,然后在37℃下将HRP与一种聚阳离子蛋白(鱼精蛋白)一起处理30分钟,导致HRP在细胞内以囊泡形式摄取。在许多囊泡、膜性限制体和液泡中发现了细胞内HRP。鱼精蛋白还诱导了局灶性自噬空泡化,并伴有进行性肌纤维变性。在没有鱼精蛋白的情况下或当孵育温度为4℃时,未检测到细胞内HRP摄取或肌肉细胞空泡化。HRP摄取的化学测定结果与形态学结果总体一致。在37℃时,鱼精蛋白存在下HRP的摄取受到刺激,而在4℃时则受到阻断。结果表明,在体外骨骼肌中,大分子的细胞内摄取是通过内吞作用发生的。

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