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自噬、异体吞噬、微自噬和分泌自噬作为细胞内降解的方式。

Autophagy, heterophagy, microautophagy and crinophagy as the means for intracellular degradation.

作者信息

Marzella L, Ahlberg J, Glaumann H

出版信息

Virchows Arch B Cell Pathol Incl Mol Pathol. 1981;36(2-3):219-34. doi: 10.1007/BF02912068.

Abstract

It is generally accepted that the lysosomal compartment plays an important role in the degradation of cellular components. In this communication we discuss various experimental models which have been used to study mechanisms of intralysosomal degradation and also discuss the evidence obtained in support of the following proposals: 1. The autophagosomes can be isolated into high purity and are the subcellular locus of induced protein degradation. 2. Different membrane components such as proteins and lipids are degraded at different rates inside the lysosomes. Intralysosomal hydrolysis is not the rate limiting step in degradation. 3. Lysosomes take up soluble material in vitro by invagination and pinching off of their membranes (microautophagy). 4. Secretory vesicles can degrade their secretory contents by fusing with the lysosomes.

摘要

人们普遍认为,溶酶体区室在细胞成分的降解中起重要作用。在本通讯中,我们讨论了用于研究溶酶体内降解机制的各种实验模型,并讨论了支持以下观点的证据:1. 自噬体可以被分离到高纯度,并且是诱导蛋白质降解的亚细胞位点。2. 不同的膜成分,如蛋白质和脂质,在溶酶体内以不同的速率降解。溶酶体内的水解不是降解的限速步骤。3. 溶酶体在体外通过膜的内陷和缢断摄取可溶性物质(微自噬)。4. 分泌囊泡可以通过与溶酶体融合来降解其分泌内容物。

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