Changes in the cell cytosol also occur during apoptosis, with variations in cellular ion concentration, pH, and level of reactive oxygen species (ROS).
- Ion indicators, including calcium, magnesium, pH, potassium and zinc
- Oxidative stress detection
Apoptosis AssaysAssays and reagents to examine the structure, function, and physiology of apoptosis |
Cell apoptosis, also known as programmed cell death, is a highly regulated process that not only allows for proper growth and development by ridding the organism of unneeded cells and tissues, but also minimizes threats to the organism by destroying surplus cells of the immune system and virus-infected or DNA-damaged cells [1].
Programmed cell death is morphologically and biochemically distinct from cell death by injury (necrosis). Unlike necrotic cells, apoptotic cells exhibit compaction of the nuclear chromatin, shrinkage of the cytoplasm, and production of membrane-bound apoptotic bodies, as well as DNA fragmentation and cleavage or degradation of several cellular proteins (Figure 1). Biochemically, apoptosis is distinguished by fragmentation of the genome and cleavage or degradation of several cellular proteins. Incorrectly regulated apoptosis is implicated in a number of disease states, including cancer, stroke, Alzheimer’s disease, and several autoimmune diseases.
Apoptosis can be induced through three different pathways: 1) targeting mitochondria functionality (mitochondrial, cellular or apoptosis intrinsic pathway), 2) direct transduction of the signal via adaptor proteins (death-receptor or apoptosis extrinsic pathway) and 3) the perforin/granzyme pathway [2-3].
Figure 1. Comparison of apoptosis and necrosis.
Identifying cells that are going through apoptosis can be challenging because many of the assays used as indicators are detecting structural and functional changes that occur in other processes as well. Additionally, no single parameter fully defines programmed cell death in all systems and the appearance of these changes can vary with apoptotic pathway or cell types. Therefore, it is often advantageous to use several different assays to detect cell apoptosis. Understanding the mechanism of cell death represents a critical aspect of toxicological profiling and plays a critical role in drug discovery efforts.
Interested in the non-apoptotic form of cell death? Learn more about Ferroptosis Research Solutions.
A distinctive feature of apoptosis is the disruption of active mitochondria, which includes changes in the membrane potential and alterations to the oxidation–reduction potential of the mitochondria.
The activation of caspase enzymes occurs very early in the apoptotic process. These enzymes have been identified as crucial mediators of the complex biochemical events associated with apoptosis.
The characteristic breakdown of the nucleus during apoptosis includes collapse and fragmentation of the DNA, degradation of the nuclear envelope and nuclear blebbing, resulting in the formation of micronuclei.
Changes in the cell’s membrane include distortion of the cell membrane, changes in the lipid composition and membrane integrity, and translocation of the phospholipid phosphatidylserine.
Changes in the cell cytosol also occur during apoptosis, with variations in cellular ion concentration, pH, and level of reactive oxygen species (ROS).
Classic products for cell viability and autophagy can also be used to help characterize and identify cells undergoing apoptosis.
Apoptosis is a highly regulated process and involves a significant number of signaling pathways. Thermo Fisher Scientific offers a wide range of primary antibodies, ELISA kits, multiplexed immunoassays, peptides and recombinant proteins as well as genomic assays targeted to specific proteins. Below is just an example of the types of assays we have available for some key apoptosis proteins.
Table 2. Example of products for key apoptosis pathway proteins.
Learn more about the Cellular Apoptosis Pathway, Apoptosis Death Receptor Pathway and the CTL-Mediated Apoptosis Pathway
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