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相关概念视频

Autophagy01:27

Autophagy

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Autophagy is a self-digesting process by which a cell protects itself from threats both within and outside the cell, ranging from abnormal proteins to invading bacteria. In this process, obsolete components of the cell and invading microbes are degraded by hydrolytic enzymes active in an acidic environment of the lysosomal lumen.
An autophagic pathway consists of a series of signaling events activated in response to diverse stress and physiological conditions such as food deprivation,...
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Delivery Pathways to the Lysosome01:36

Delivery Pathways to the Lysosome

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Eukaryotic cells use different mechanisms to eliminate toxic waste obsolete and worn-out substances. Lysosomes play a pivotal role in this, and hence, these substances are carried to the lysosome from other parts of the cell and extracellular space through different pathways. The most elaborately studied pathways to the lysosome are the endocytic pathways.
Endocytosis
In endocytosis, the cell membrane takes up macromolecules and particles from the surrounding medium. Clathrin-mediated...
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Autophagic Cell Death01:18

Autophagic Cell Death

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Christian de Duve discovered “autophagy,” a process in which cellular components are engulfed by membrane-bound organelles called autophagosomes. The autophagosomes then fuse with lysosomes to digest the enclosed contents. Autophagy is generally activated in cells to prevent cell death. However, cell death is triggered when the damage is beyond repair.
Autophagy and Apoptosis
Autophagy can activate apoptosis. In normal conditions, the autophagy activating protein Beclin-1 and...
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Overview of Cell Death01:30

Overview of Cell Death

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Cell death is an essential process where the body gets rid of old or damaged cells. Cell proliferation and death need to be balanced, as an imbalance between the two may lead to cancer or autoimmune diseases.
Cell death was observed in the early 19th century, but there was no experimental evidence to prove it. In 1842, Carl Vogt first discovered cell death in a metamorphic toad; however, it was not termed ‘cell death.’ Scientists discovered different cell death pathways only in the...
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Phagocytosis00:41

Phagocytosis

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Cells pull particles inward and engulf them in spherical vesicles in an energy-requiring process called endocytosis. Phagocytosis (“cellular eating”) is one of three major types of endocytosis. Cells use phagocytosis to take in large objects—such as other cells (or their debris), bacteria, and even viruses.
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The Proteasome01:13

The Proteasome

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Eukaryotic cells can degrade proteins through several pathways. One of the most important among these is the ubiquitin-proteasome pathway. It helps the cell eliminate the misfolded, damaged, or unwarranted cytoplasmic proteins in a highly specific manner.
In this pathway, the target proteins are first tagged with small proteins called ubiquitin. This involves participation of a series of enzymes including— E1 (ubiquitin-activating enzyme), E2 (ubiquitin-conjugating enzyme), and E3...
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相关实验视频

Updated: Jul 28, 2025

Exploring the Regulation of Lipid Droplet Catabolism through Lipophagy
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Exploring the Regulation of Lipid Droplet Catabolism through Lipophagy

Published on: January 31, 2025

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一眼看的侵略性.

Bernd Bauer1,2, Sascha Martens1, Luca Ferrari1

  • 1Max Perutz Labs, University of Vienna, Vienna BioCenter, Dr Bohr-Gasse 9/5, 1030 Vienna, Austria.

Journal of cell science
|May 31, 2023
PubMed
概括
此摘要是机器生成的。

蛋白质稳定网络维持细胞功能;其衰减导致与衰老和疾病相关的蛋白质聚合物的积累. 这项研究概述了聚合物,一种清除这些聚合物的途径,以及其治疗潜力.

关键词:
自自是一种自的过程.神经退行发生神经退行.蛋白质定位网络的蛋白质定位网络.

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相关实验视频

Last Updated: Jul 28, 2025

Exploring the Regulation of Lipid Droplet Catabolism through Lipophagy
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Exploring the Regulation of Lipid Droplet Catabolism through Lipophagy

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Analyzing Starvation-Induced Autophagy in the Drosophila melanogaster Larval Fat Body
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Analyzing Starvation-Induced Autophagy in the Drosophila melanogaster Larval Fat Body

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Live Cell Imaging of Early Autophagy Events: Omegasomes and Beyond
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科学领域:

  • 细胞生物学 细胞生物学
  • 分子机制的分子机制
  • 疾病的病原发生 疾病的病原发生

背景情况:

  • 蛋白质稳定网络,包括陪伴者,无处不在的蛋白质酶系统和自,维持细胞蛋白质酶的功能.
  • 蛋白质稳定性下降导致蛋白质聚合物的积累,这是衰老和各种疾病的标志.
  • 蛋白质聚合物破坏细胞功能,并与神经退行性和其他病理有关.

研究的目的:

  • 为了提供对食的概述,选择性自的途径用于去除蛋白质聚合物.
  • 阐明聚合酶的调节机制,包括翻译后的修饰和辅助蛋白.
  • 讨论聚合在神经元生理学中的作用及其在疾病中的失调.

主要方法:

  • 通过选择性自来控制蛋白质聚合物清除的分子机制的审查.
  • 对控制食的调节途径的分析.
  • 检查聚合物在特定疾病中的参与,特别是神经元中的参与.

主要成果:

  • 聚是选择性去除有毒蛋白质聚合物的关键途径.
  • 翻译后的修饰和辅助蛋白质在调节食过程中起着至关重要的作用.
  • 侵蚀细胞的破坏有助于蛋白质聚合疾病,特别是在神经元细胞中.

结论:

  • 了解食机制对于理解衰老和疾病至关重要.
  • 向和重编程聚合蛋白为蛋白质聚合障碍提供了一个有前途的治疗策略.
  • 对食路径的进一步研究可以为衰弱性疾病提供新的治疗方法.