Cell Protection and Crystal Endocytosis Inhibition by Sulfated Laminaria Polysaccharides Against Nano-COM-Induced Oxidative Damage in Renal Epithelial Cells.
Bang-Xian YuYi-Han ZhangChun-Yao LiJun-Yi XianShu-Jue LiWei-Bo HuangLing-Hong HuangXin-Yuan SunPublished in: ACS omega (2023)
Background : The damage to renal tubular epithelial cells is closely related to the formation of kidney stones. At present, research on drugs that can protect cells from damage remains limited. Methods : This study aims to explore the protective effects of four different sulfate groups (-OSO 3 - ) of Laminaria polysaccharides (SLPs) on human kidney proximal tubular epithelial (HK-2) cells and determine the difference in the endocytosis of nano-sized calcium oxalate monohydrate (COM) crystals before and after protection. COM with a size of 230 ± 80 nm was used to damage HK-2 cells to establish a damage model. The protection capability of SLPs (LP0, SLP1, SLP2, and SLP3) with -OSO 3 - contents of 0.73, 15, 23, and 31%, respectively, against COM crystal damage and the effect of SLPs on the endocytosis of COM crystals were studied. Results : Compared with that of the SLP-unprotected COM-injured group, the cell viability of the SLP-protected group was improved, healing capability was enhanced, cell morphology was restored, production of reactive oxygen species was reduced, mitochondrial membrane potential and lysosome integrity were increased, intracellular Ca 2+ level and autophagy were decreased, cell mortality was reduced, and internalized COM crystals were lessened. The capability of SLPs to protect cells from damage and inhibit the endocytosis of crystals in cells enhanced with an increase in the -OSO 3 - content of SLPs. Conclusions : SLPs with a high -OSO 3 - content may become a potential green drug for preventing the formation of kidney stones.
Keyphrases
- oxidative stress
- induced apoptosis
- high glucose
- cell cycle arrest
- reactive oxygen species
- single cell
- endothelial cells
- cell therapy
- room temperature
- diabetic rats
- cell death
- stem cells
- signaling pathway
- risk factors
- mesenchymal stem cells
- coronary artery disease
- risk assessment
- climate change
- cell proliferation
- ionic liquid