1.Role of Nrf2/HO-1 signal axis in the mechanisms for oxidative stress-relevant diseases.
Tiantian WANG ; Chunyuan CHEN ; Lei YANG ; Zhihui ZENG ; Maojun ZENG ; Wen JIANG ; Lin LIU ; Mingyi ZHAO
Journal of Central South University(Medical Sciences) 2019;44(1):74-80
In the development of oxidative stress-relevant diseases, reactive oxygen species (ROS) removal obstacle or excess production results in the damage of the body tissues and organs. Recent studies have demonstrated that nuclear factor E2-related factor 2/heme oxygenase-1 (Nrf2/HO-1) axis played a significant role in anti-oxidative stress. The Nrf2/HO-1 axis counteracts oxidative stress injury by its resistance to inflammation, oxidation, mitochondrial damage and calcium influx, apoptosis, pyroptosis, ferroptosis and autophagy, which provides a theoretical basis for its therapeutic effect on various oxidative stress-relevant diseases in multiple organs (respiratory, cardiovascular, nervous, digestive, urinary and blood systems). Therefore, effective regulation of the Nrf2/HO-1 signal axis can be an important strategy for treatment of oxidative stress-relevant diseases.
Heme Oxygenase-1
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NF-E2-Related Factor 2
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Oxidative Stress
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Reactive Oxygen Species
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Signal Transduction
2.Cryo-EM structures of the mammalian endo-lysosomal TRPML1 channel elucidate the combined regulation mechanism.
Sensen ZHANG ; Ningning LI ; Wenwen ZENG ; Ning GAO ; Maojun YANG
Protein & Cell 2017;8(11):834-847
TRPML1 channel is a non-selective group-2 transient receptor potential (TRP) channel with Ca permeability. Located mainly in late endosome and lysosome of all mammalian cell types, TRPML1 is indispensable in the processes of endocytosis, membrane trafficking, and lysosome biogenesis. Mutations of TRPML1 cause a severe lysosomal storage disorder called mucolipidosis type IV (MLIV). In the present study, we determined the cryo-electron microscopy (cryo-EM) structures of Mus musculus TRPML1 (mTRPML1) in lipid nanodiscs and Amphipols. Two distinct states of mTRPML1 in Amphipols are added to the closed state, on which could represent two different confirmations upon activation and regulation. The polycystin-mucolipin domain (PMD) may sense the luminal/extracellular stimuli and undergo a "move upward" motion during endocytosis, thus triggering the overall conformational change in TRPML1. Based on the structural comparisons, we propose TRPML1 is regulated by pH, Ca, and phosphoinositides in a combined manner so as to accommodate the dynamic endocytosis process.
Animals
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Calcium
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metabolism
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Cryoelectron Microscopy
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Endocytosis
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Endosomes
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metabolism
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Gene Expression
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HEK293 Cells
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Humans
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Hydrogen-Ion Concentration
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Lysosomes
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metabolism
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Mice
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Models, Biological
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Mucolipidoses
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genetics
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metabolism
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pathology
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Nanostructures
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chemistry
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ultrastructure
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Phosphatidylinositols
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metabolism
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Transgenes
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Transient Receptor Potential Channels
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chemistry
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genetics
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metabolism
3.Structure of intact human MCU supercomplex with the auxiliary MICU subunits.
Wei ZHUO ; Heng ZHOU ; Runyu GUO ; Jingbo YI ; Laixing ZHANG ; Lei YU ; Yinqiang SUI ; Wenwen ZENG ; Peiyi WANG ; Maojun YANG
Protein & Cell 2021;12(3):220-229