TABLE 4.
Cell death type | Basic features | Biochemical features | Morphological features | Detection methods |
---|---|---|---|---|
Apoptosis | Type1 programmed cell death | Activation of caspases, oligonucleosomal DNA fragmentation | Plasma membrane blebbing, nuclear condensation and fragmentation, apoptotic bodies | TUNEL, DNA ladder, DNA content analysis, apoptosis enzyme-linked immunoassay, annexin binding assay, LDH activity assay, mitochondrial membrane potential assay |
Reversible | ||||
Autophagy | Type2 programmed cell death | Increased lysosomal activity, LC3I to LC3II transformation | Formation of double-membraned autolysosomes | Western blotting or Fluorescence Microscopy of LC3 (marker protein for autophagosomes) and p62 (autophagy substrate) |
Reversible | ||||
Ferroptosis | Reversible | Iron and ROS accumulation, inhibition of xCT and reduced GSH. | Increased density of outer cell membrane, ruptured outer mitochondrial membrane | Iron assay kit, GSSG/GSH Quantification kit, Glutamine assay kit |
Abbreviations used: ROS, reactive oxygen species; xCT, light-chain subunit of SLC7A11 (system xc− cystine/glutamate antiporter); GSH, glutathione; GSSG, oxidized glutathione; LDH, lactate dehydrogenase.