自噬体积累诱导剂抑制肝细胞蛋白降解。

Acta biologica et medica Germanica Pub Date : 1982-01-01
A L Kovács, P O Seglen
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引用次数: 0

摘要

在已知的9种诱导自噬体积累的化合物中,有7种被发现抑制内源性蛋白的降解,所有这些化合物都抑制分离的大鼠肝细胞中外源性蛋白(asialofetuin)的降解。基于这些发现,我们提出了两种可能的药物引起自噬体积累的共同机制:1)抑制蛋白质降解可能导致细胞内氨基酸水平降低,这一变化反过来又刺激了自噬隔离的增加。2)溶酶体功能紊乱可降低其与新形成的自噬体融合的能力,从而引起自噬体的积累。
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Inhibition of hepatocytic protein degradation by inducers of autophagosome accumulation.

Out of nine compounds known to induce accumulation of autophagosomes, seven were found to inhibit degradation of endogenous protein and all of them to inhibit degradation of an exogenous protein (asialofetuin) in isolated rat hepatocytes. On the basis of these findings we propose two possible common mechanisms by which the drugs may cause autophagosome accumulation: 1) The inhibition of protein degradation may result in a decrease in the intracellular amino acid levels, a change which in turn serves as a stimulus for increased autophagic sequestration. 2) Disturbance of the function of the lysosomes may reduce their ability to fuse with newly formed autophagosomes, thereby causing accumulation of the latter.

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