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. 2022 Jan 18;9:789948. doi: 10.3389/fcell.2021.789948

TABLE 3.

Osteoarthritis pathogenesis Cell Death Types
Pyroptosis Apoptosis Necroptosis Ferroptosis
Increased inflammatory component IL-1β↑, IL-18↑, Caspase-1↑, NLRP3↑, MMP-1↑, MMP-13↑, NLRP3↑, NLRP1↑ IL-1β↑, IL-6↑, IL-8↑, TNF-α↑, Bax↑, Bcl-2↑, ROS↑, MMP2↑, MMP9↑ MLKL↑, Cleaved caspase8↑, p-MLKL↑ Expression of catabolic genes Mmp3↑, Mmp13↑, Adamts5↑, Ptsg2↑, Col10a1↑
Mechanical overload IL-1β↑, IL-18↑, Caspase-1↑, NLRP3↑, MMP-1↑, MMP-13↑ Cleaved caspase-3, -6, -7, and -8↑, actin polymerization↑ RIP1↑, RIP3↑, Caspase-8↑, ROS↑, Mitochondrial membrane potential↓ MMP13↑, collagen II↓
Metabolic alterations Caspase-1↑, IL-1β↑, IL-18↑, Gasdermin-D↑ Phospho-fructose kinase 1 (Pfk1) l↓, hexokinase II (Hk2) l↓, ATP l↓, mitochondrial fusion Inhibits necroptosis through the hypermethylation of the promoter Reactive oxygen species (ROS) ↑, lipid ROS↑, MMP13↑, collagen II↓
Cell senescence IL-1β↑, IL-18↑, activation caspase-1 or caspase-11 COL10A1↑, IL-1↑, TNF-α↑, MMP-13↑, ADAMTS5↑, COL2A1↓ Oxidative stress↑, mTOR signaling↑, DAMPs↑ Mmp3↑, Mmp13↑, Adamts5↑, Ptsg2↑, Col10a1↑