Three decades of caspases and RIPKs in life and death

R K Subbarao Malireddi1, Thirumala-Devi Kanneganti1

  • 1Department of Immunology, St. Jude Children's Research Hospital, 262 Danny Thomas Pl, Memphis, TN 38105, United States.

PubMed

Insights

Caspases and RIPK kinases regulate cell death and immunity. Genetic studies reveal their role in PANoptosis, an inflammatory cell death pathway, offering new therapeutic targets for diseases like cancer and neurodegeneration.

Area of Science:

  • Molecular Biology
  • Immunology
  • Cell Biology

Background:

  • Caspases and RIPK kinases are key regulators of cell death and innate immunity.
  • Dysregulation of these molecules contributes to inflammation and disease.
  • Decades of genetic research have uncovered their complex roles.

Purpose of the Study:

  • To review genetic studies on caspases and RIPKs.
  • To synthesize findings on their roles in development, cell death, inflammation, and disease.
  • To highlight the emerging concept of PANoptosis.

Main Methods:

  • Review of three decades of genetic studies.
  • Synthesis of seminal findings across multiple biological areas.
  • Analysis of molecular mechanisms and disease relevance.

Main Results:

  • Caspases and RIPKs are critical for host defense, development, and tumor immunity.
  • Their activation can drive aberrant inflammation and disease pathology.
  • The concept of PANoptosis, an innate immune inflammatory cell death pathway, has been established.
  • PANoptosis is mediated by PANoptosome complexes involving caspases and RIPKs, notably Caspase-8.
  • Caspases and RIPKs, through PANoptosis, are implicated in infections, inflammatory conditions, cytokine storm, and cancer.

Conclusions:

  • Genetic and biochemical evidence supports targeting PANoptosome pathway molecules.
  • Therapeutic strategies targeting innate immune sensors, caspases, and RIPKs show promise.
  • These targets could be beneficial for neurodegeneration, metabolic disorders, cancers, and autoimmune diseases.

Related Concept Videos

Caspases01:24

Caspases

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...
12.7K
Overview of Cell Death01:30

Overview of Cell Death

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...
7.8K
The Extrinsic Apoptotic Pathway01:17

The Extrinsic Apoptotic Pathway

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...
6.6K
Regulation of the Unfolded Protein Response01:31

Regulation of the Unfolded Protein Response

Inositol-requiring kinase one or IRE1 is the most conserved eukaryotic unfolded protein response (UPR) receptor. It is a type I transmembrane protein kinase receptor with a distinctive site-specific RNase activity. As the binding mechanics of the misfolded proteins with the N-terminal domain of IRE-1 are unclear, three binding models — direct, indirect, and allosteric -- are proposed for receptor activation. Nevertheless, it is known that once a misfolded protein associates with IRE1, it...
2.6K
The Intrinsic Apoptotic Pathway01:31

The Intrinsic Apoptotic Pathway

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...
6.9K
Necrosis01:16

Necrosis

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...
4.8K