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相关概念视频

Necrosis01:16

Necrosis

5.2K
Necrosis is considered as an “accidental” or unexpected form of cell death that ends in cell lysis. The first noticeable mention of “necrosis” was in 1859 when Rudolf Virchow used this term to describe advanced tissue breakdown in his compilation titled “Cell Pathology”.
Morphological Manifestations of Necrosis
Necrotic cells show different types of morphological appearance depending on the type of tissue and infection. In coagulative necrosis, cells become...
5.2K
Overview of Cell Death01:30

Overview of Cell Death

7.6K
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...
7.6K
Cellular Injury IV: Necrosis01:16

Cellular Injury IV: Necrosis

57
Necrosis is a form of irreversible cell death caused by severe injury such as ischemia, toxins, or trauma. Unlike programmed cell death, it is an uncontrolled, pathological process that typically provokes inflammation in surrounding tissues.Pathophysiologic ChangesNecrosis begins when cells sustain critical damage, leading to swelling of organelles, particularly mitochondria, and rapid ATP depletion. As energy levels decline, membrane ion pumps fail, leading to calcium influx and eventually,...
57
Apoptosis01:30

Apoptosis

11.9K
Apoptosis is a combination of two Greek words, 'apo' and 'ptosis,' meaning separation and falling off, respectively. Hippocrates used this word to describe gangrene, which was caused due to bandaging of fractured bones. Apoptosis was distinguished from necrosis in 1970 when John Kerr reported observations of morphological changes occurring during apoptosis. During one experiment, he observed that the disruption of blood supply to the liver tissue resulted in a size...
11.9K
Autophagic Cell Death01:18

Autophagic Cell Death

3.3K
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...
3.3K
Phagocytosis of Apoptotic Cells01:17

Phagocytosis of Apoptotic Cells

3.9K
Cells undergoing apoptosis form apoptotic bodies that must be removed immediately to prevent inflammation, autoimmune diseases, and necrosis. Phagocytosis is carried out by professional phagocytes such as macrophages or  immature dendritic cells. Non-professional phagocytes such as  epithelial cells and fibroblasts also take part in this process; however, they are not as effective as professional phagocytes. 
Normal cells contain receptors that prevent them from being recognized...
3.9K

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Void-X: A generative void-filling model for predicting atomic packing in proteins.

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Glucose hypometabolism and hyperphosphorylated Tau synergistically drive neuronal necroptosis.

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Cell death in cancer.

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Correction: Bax and Bak can localize to the endoplasmic reticulum to initiate apoptosis.

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相关实验视频

Updated: Apr 26, 2026

Characterization of MLKL-mediated Plasma Membrane Rupture in Necroptosis
08:55

Characterization of MLKL-mediated Plasma Membrane Rupture in Necroptosis

Published on: August 7, 2018

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快照:死细胞灭

Wen Zhou1, Junying Yuan1

  • 1Department of Cell Biology, Harvard Medical School, Boston, MA 02115, USA.

Cell
|July 19, 2014
PubMed
概括

亡,一种涉及RIPK1和RIPK3的调节性亡形式,在炎症和细胞死亡中起作用. 抑制这种途径显示出治疗各种疾病的前景.

科学领域:

  • 分子生物学分子生物学
  • 细胞生物学 细胞生物学
  • 免疫学 免疫学 免疫学

背景情况:

  • 亡是一种受调节的亡形式.
  • 它与亡不同,涉及特定的信号通路.
  • 关键介质包括RIPK1和RIPK3激酶.

研究的目的:

  • 为了阐明亡的信号通路.
  • 探索抑制亡的治疗潜力.

主要方法:

  • 研究了RIPK1和RIPK3在亡中的作用.
  • 分析了体形成和MLKL激活.
  • 在疾病的小鼠模型中评估了亡抑制.

主要成果:

  • 亡是由RIPK1和RIPK3激酶活性介导的.
  • 该途径涉及体形成和MLKL激活.
  • 在小鼠模型中,抑制亡减少了病理学.

结论:

  • 亡是关键的调节细胞死亡途径.
  • 向死细胞灭绝为涉及炎症和细胞死亡的疾病提供了潜在的治疗策略.

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Live-cell Imaging of Lysosomal Membrane Permeabilization During Necroptosis

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Author Spotlight: THP-1 Macrophage Response to LPS/ATP &#8212; Unveiling the Pyroptosis, Apoptosis, and Necroptosis Spectrum
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Author Spotlight: THP-1 Macrophage Response to LPS/ATP — Unveiling the Pyroptosis, Apoptosis, and Necroptosis Spectrum

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Characterization of MLKL-mediated Plasma Membrane Rupture in Necroptosis
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Characterization of MLKL-mediated Plasma Membrane Rupture in Necroptosis

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Live-cell Imaging of Lysosomal Membrane Permeabilization During Necroptosis

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Author Spotlight: THP-1 Macrophage Response to LPS/ATP &#8212; Unveiling the Pyroptosis, Apoptosis, and Necroptosis Spectrum
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Author Spotlight: THP-1 Macrophage Response to LPS/ATP — Unveiling the Pyroptosis, Apoptosis, and Necroptosis Spectrum

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