Related Experiment Video
Updated: Jul 4, 2025

06:52
Detection of Inflammasome Activation and Pyroptotic Cell Death in Murine Bone Marrow-derived Macrophages
Published on: May 21, 2018
10.7K
Crosstalk between inflammasome sensors and DNA damage response pathways
Delphine Burlet1,2,3,4, Anne-Laure Huber1,2,3,4, Agnès Tissier1,2,3,4
1INSERM U1052, Centre de Recherche en Cancérologie de Lyon, France.
The FEBS Journal
|January 26, 2024
Summary
Inflammasomes, known for inflammation, also interact with the DNA damage response (DDR). This review explores how DDR affects inflammasomes and how inflammasomes protect genome integrity.
Area of Science:
- Cellular Biology
- Molecular Biology
- Immunology
Background:
- Eukaryotic cells possess defense mechanisms against various threats.
- Inflammasomes are key regulators of inflammatory responses, particularly against infections.
- Emerging evidence points to inflammasomes' roles beyond inflammation, including in cellular stress responses.
Purpose of the Study:
- To review the intricate relationship between inflammasomes and the DNA damage response (DDR).
- To explore the reciprocal influence between inflammasome activation and DDR pathways.
- To identify shared signaling pathways and activation cues for both inflammasomes and DDR.
Main Methods:
- Literature review of recent studies on inflammasomes and DDR.
- Analysis of molecular mechanisms linking inflammasome sensors and DDR pathways.
- Synthesis of findings on common activators and regulatory networks.
Main Results:
- The DNA damage response (DDR) influences inflammasome activation.
- Inflammasomes play a role in preserving genome integrity and impact DDR.
- Novel functions of inflammasome sensors within DDR pathways have been identified.
Conclusions:
- The interplay between inflammasomes and DDR is crucial for cellular integrity.
- Shared signaling pathways likely govern the activation of both inflammasomes and DDR.
- Understanding these connections offers insights into cellular defense strategies and potential therapeutic targets.
Related Concept Videos
The Extrinsic Apoptotic Pathway
6.4K
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...
6.4K
The Intrinsic Apoptotic Pathway
6.6K
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...
6.6K
Interactions Between Signaling Pathways
6.3K
Signaling cascades usually lack linearity. Multiple pathways interact and regulate one another, allowing cells to integrate and respond to diverse environmental stimuli.
Convergence and divergence, and cross-talk between signaling pathways
Two distinct signaling pathways can converge on a single functional unit, which may either be a single protein or a complex of proteins. The response is either functionally distinct or synergistic between the two pathways but different from the response...
Convergence and divergence, and cross-talk between signaling pathways
Two distinct signaling pathways can converge on a single functional unit, which may either be a single protein or a complex of proteins. The response is either functionally distinct or synergistic between the two pathways but different from the response...
6.3K
NF-κB-dependent Signaling Pathway
7.4K
The transcription factor NF-κB was discovered in 1986 in the lab of Nobel laureate Professor David Baltimore, for its interaction with the immunoglobulin light chain enhancer in B-cells. After more than three decades of study, it is now evident that NF-κB regulates the expression of over 100 genes. Most of these genes play an essential role in the innate and adaptive immune responses as well as the inflammatory responses of animals.
NF-κB-dependent Signaling Mechanism
The...
NF-κB-dependent Signaling Mechanism
The...
7.4K
DNA Damage can Stall the Cell Cycle
9.2K
In response to DNA damage, cells can pause the cell cycle to assess and repair the breaks. However, the cell must check the DNA at certain critical stages during the cell cycle. If the cell cycle pauses before DNA replication, the cells will contain twice the amount of DNA. On the other hand, if cells arrest after DNA replication but before mitosis, they will contain four times the normal amount of DNA. With a host of specialized proteins at their disposal,cells must use the right protein at...
9.2K
Caspases
12.5K
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...
12.5K

