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Related Concept Videos

The Extrinsic Apoptotic Pathway01:17

The Extrinsic Apoptotic Pathway

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The extrinsic apoptotic pathway is initiated when extracellular death-inducing signals, such as specific cytokines, activate the death receptors expressed on the cell surface. The immune cells involved in this pathway are natural killer cells (NK cells) and cytotoxic T-lymphocytes. NK cells are critical in innate immune response, while cytotoxic T-lymphocytes are associated with adaptive immune response. These cells recognize specific receptors expressed on the altered cells and activate...
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Caspase, a family of cysteine proteases, serve as effectors in apoptosis. The ced3 gene in C.elegans was first identified to be involved in apoptosis. This gene encodes the ced-3 caspase that is similar to the interleukin-1-beta converting enzyme or ICE in mammals. In addition to apoptosis, caspases also function in the inflammatory response. Inflammatory caspases are essential in activating pro-inflammatory cytokines that recruit immune cells and block the replication of pathogens inside...
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Internal cellular stress, such as cellular injury or hypoxia, triggers intrinsic apoptosis. The B-cell lymphoma 2 (Bcl-2) family of proteins are the primary regulators of the intrinsic apoptotic pathway. For example, during DNA damage, checkpoint proteins, such as Ataxia Telangiectasia Mutated (ATM protein) and Checkpoints Factor-2 (Chk2) proteins, are activated. These proteins phosphorylate p53 which further activates pro-apoptotic proteins, such as Bax, Bak, PUMA, and Noxa, and inhibits...
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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. 
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Integrins act both as extracellular input receivers and as intracellular processing activators. As their name suggests, integrins are entirely integrated into the membrane structure. Their hydrophobic membrane-spanning regions interact with the phospholipid bilayer's hydrophobic region. These membrane receptors provide extracellular attachment sites for effectors like hormones and growth factors. They activate intracellular response cascades when their effectors are bound and active.
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Related Experiment Video

Updated: Dec 17, 2025

Detection of Inflammasome Activation and Pyroptotic Cell Death in Murine Bone Marrow-derived Macrophages
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Inflammasomes.

Natália Ketelut-Carneiro1, Katherine A Fitzgerald1

  • 1Program in Innate Immunity, Division of Infectious Diseases and Immunology, Department of Medicine, University of Massachusetts Medical School, Worcester, MA 01605, USA.

Current Biology : CB
|June 24, 2020
PubMed
Summary

This review covers inflammasomes, which are protein complexes crucial for immunity. Understanding inflammasome activation and function is key to developing treatments for inflammatory diseases and infections.

Area of Science:

  • Immunology
  • Molecular Biology
  • Cellular Biology

Background:

  • Inflammasomes are multiprotein complexes central to innate immunity.
  • They play a critical role in host defense against pathogens and in inflammatory conditions.

Purpose of the Study:

  • To provide a comprehensive overview of inflammasome biology.
  • To discuss the composition, assembly, and activation mechanisms of inflammasomes.
  • To explore the effector functions and involvement of inflammasomes in disease.

Main Methods:

  • Literature review and synthesis of existing research on inflammasomes.

Main Results:

  • Detailed explanation of inflammasome components and their interactions.

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  • Elucidation of inflammasome activation pathways.
  • Discussion of inflammasome-mediated inflammatory responses and their pathological implications.
  • Conclusions:

    • Inflammasomes are critical regulators of inflammation and immunity.
    • Dysregulation of inflammasome pathways contributes to various inflammatory diseases.
    • Targeting inflammasomes holds therapeutic potential for infectious and inflammatory disorders.