Area of research
Physiology · Immunology
Research interest
Research interests include PIEZO1, Fibrosis, Chemistry, Inflammation, Kidney, and Macrophage.
Gut‐derived bacterial vesicles carrying lipopolysaccharide promote microglia‐mediated synaptic pruning
Piezo1 aggravates ischemia/reperfusion-induced acute kidney injury by Ca <sup>2+</sup> -dependent calpain/HIF-1α/Notch signaling
Endothelial Piezo1 stimulates angiogenesis to offer protection against intestinal ischemia–reperfusion injury in mice
Lithospermic acid improves diabetic kidney fibrosis by regulating Piezo1/TGF-β1/Smad signaling pathway
Myeloid Piezo1 Improves Inflammation Resolution and Phagocytosis in Acute Liver Injury
Lithospermic acid alleviates myocardial ischemia/reperfusion injury by inhibiting mitophagy via the Piezo1-PPP3/calcineurin-TFEB pathway
Guizhitongluo Tablet inhibits atherosclerosis and foam cell formation through regulating Piezo1/NLRP3 mediated macrophage pyroptosis
Lithospermic acid improves liver fibrosis through Piezo1-mediated oxidative stress and inflammation
Cardiomyocyte-specific Piezo1 deficiency mitigates ischemia-reperfusion injury by preserving mitochondrial homeostasis
Piezo1 specific deletion in macrophage protects the progression of liver fibrosis in mice: Erratum
Piezo1 specific deletion in macrophage protects the progression of liver fibrosis in mice
Nuanxinkang (NXK) ameliorates Piezo1-mediated pyroptosis post-myocardial infarction
Myeloid <i>Piezo1</i> Deletion Protects Renal Fibrosis by Restraining Macrophage Infiltration and Activation
Inhibition of chemically and mechanically activated Piezo1 channels as a mechanism for ameliorating atherosclerosis with salvianolic acid B
Dingxin Recipe IV attenuates atherosclerosis by regulating lipid metabolism through LXR-α/SREBP1 pathway and modulating the gut microbiota in ApoE-/- mice fed with HFD