PP1A prevents ROS-induced pyroptosis by inhibiting MAPK/caspase-3 in mouse adipose tissue.
Yizhe ChenMeng CheChaowei LiYizhou LiTiantian ZhangXinjian LiChao SunPublished in: The FEBS journal (2022)
Pyroptosis is a type of programmed cell death triggered by a variety of exogenous stimuli, playing important roles in the development of cells. Recent studies have shown that pyroptosis also occurs in human and mouse adipocytes. The serine/threonine protein phosphatase 1 catalytic subunit α (PP1A) is located in the nucleus and functions in the regulation of cell development, glucose metabolism and protein synthesis. PP1A can also target important proteins in the process of apoptosis. However, it is still unclear whether PP1A participates in the regulation of pyroptosis in mouse adipocytes. In the present study, we investigated the function of PP1A in reactive oxygen species-induced pyroptosis and the related mechanism in mouse adipose tissue. Our results demonstrated that PP1A suppressed pyroptosis in adipocytes by inhibiting the reactive oxygen species/mitogen-activated protein kinase/caspase-3 signaling pathway and promoting M2 macrophage polarization. This experiment provides a theoretical basis for understanding the regulatory function and mechanism of PP1A in pyroptosis caused by oxidative stress in adipocytes.
Keyphrases
- adipose tissue
- nlrp inflammasome
- signaling pathway
- induced apoptosis
- reactive oxygen species
- oxidative stress
- cell death
- diabetic rats
- cell cycle arrest
- protein kinase
- insulin resistance
- endoplasmic reticulum stress
- pi k akt
- high fat diet
- dna damage
- high glucose
- transcription factor
- cell therapy
- single cell
- drug induced
- mass spectrometry
- bone marrow
- mouse model
- high resolution
- induced pluripotent stem cells
- protein protein