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自噬溶酶体再形成。

Autophagic lysosome reformation.

机构信息

State Key Laboratory of Biomembrane and Membrane Biotechnology, Tsinghua University-Peking University Joint Center for Life Sciences, School of Life Sciences, Tsinghua University, Beijing 100084, China.

出版信息

Exp Cell Res. 2013 Jan 15;319(2):142-6. doi: 10.1016/j.yexcr.2012.09.004. Epub 2012 Sep 19.

DOI:10.1016/j.yexcr.2012.09.004
PMID:22999865
Abstract

Autophagy is an evolutionarily conserved lysosome-dependent degradation pathway. In recent years, many important advances have been made in understanding the cellular and molecular mechanism of autophagosome formation. However, the late stages of autophagy-the cellular events after formation of the autolysosome-are relatively rarely studied. In this review, we discussed the cellular process and molecular mechanism of autophagic lysosome reformation, a cellular events which defines the terminal stage of autophagy.

摘要

自噬是一种进化上保守的溶酶体依赖性降解途径。近年来,人们在理解自噬体形成的细胞和分子机制方面取得了许多重要进展。然而,自噬的晚期阶段——即自噬溶酶体形成后的细胞事件——相对较少被研究。在这篇综述中,我们讨论了自噬溶酶体再形成的细胞过程和分子机制,这一细胞事件定义了自噬的终末阶段。

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Autophagic lysosome reformation.自噬溶酶体再形成。
Exp Cell Res. 2013 Jan 15;319(2):142-6. doi: 10.1016/j.yexcr.2012.09.004. Epub 2012 Sep 19.
2
Recent progress in autophagic lysosome reformation.自噬性溶酶体再形成的最新进展
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Spinster is required for autophagic lysosome reformation and mTOR reactivation following starvation.不育是自噬溶酶体重构和饥饿后 mTOR 重新激活所必需的。
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Spatio-temporal association between mTOR and autophagy during cellular senescence.细胞衰老过程中 mTOR 与自噬的时空关联。
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Varicella-zoster virus inhibits autophagosome-lysosome fusion and the degradation stage of mTOR-mediated autophagic flux.水痘-带状疱疹病毒抑制自噬体-溶酶体融合和 mTOR 介导的自噬流的降解阶段。
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Autophagic lysosomal reformation depends on mTOR reactivation in H2O2-induced autophagy.自噬性溶酶体再形成依赖于过氧化氢诱导的自噬中mTOR的重新激活。
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