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从烟草BY-2细胞中分离自噬溶酶体。

Isolation of Autolysosomes from Tobacco BY-2 Cells.

作者信息

Takatsuka Chihiro, Inoue-Aono Yuko, Moriyasu Yuji

机构信息

Tokai University Junior College, Shizuoka, Japan.

Graduate School of Science and Engineering, Saitama University, 255 Shimo-Okubo, Sakura-ku, Saitama-shi, Saitama, 338-8570, Japan.

出版信息

Methods Mol Biol. 2017;1511:151-161. doi: 10.1007/978-1-4939-6533-5_12.

Abstract

Autolysosomes are organelles that sequester and degrade a portion of the cytoplasm during autophagy. Although autophagosomes are short lived compared to other organelles such as mitochondria, plastids, and peroxisomes, many autolysosomes accumulate in tobacco BY-2 cells cultured under sucrose starvation conditions in the presence of a cysteine protease inhibitor. We here describe our methodology for isolating autolysosomes from BY-2 cells by conventional cell fractionation using a Percoll gradient. The autolysosome fraction separates clearly from fractions containing mitochondria and peroxisomes. It contains acid phosphatase, vacuolar H-ATPase, and protease activity. Electron micrographs show that the fraction contains partially degraded cytoplasm seen in autolysosomes before isolation although an autolysosome structure is only partially preserved.

摘要

自噬溶酶体是在自噬过程中隔离并降解部分细胞质的细胞器。尽管与线粒体、质体和过氧化物酶体等其他细胞器相比,自噬体寿命较短,但在存在半胱氨酸蛋白酶抑制剂的情况下,蔗糖饥饿条件下培养的烟草BY-2细胞中会积累许多自噬溶酶体。我们在此描述了通过使用Percoll梯度的常规细胞分级分离从BY-2细胞中分离自噬溶酶体的方法。自噬溶酶体组分与含有线粒体和过氧化物酶体的组分明显分离。它含有酸性磷酸酶、液泡H-ATP酶和蛋白酶活性。电子显微镜照片显示,该组分含有分离前自噬溶酶体中可见的部分降解的细胞质,尽管自噬溶酶体结构仅部分保留。

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