The TLR4/ HIF⁃1α signaling pathway mediates glycated low density lipoprotein induced injury of human umbilical vein endothelial cells
10.19405/j.cnki.issn1000-1492.2022.10.019
- Author:
Junhui Qiu
1
;
Meizhi Liu
2
;
Dusang Sun
2
;
Ting Pan
3
;
Weiwei Zhao
2
;
Wenjun Sha
2
;
Jun Lu
2
;
Tao Lei
1
,
2
Author Information
1. Shanghai Putuo Central School of Clinical Medicine , Anhui Medical University , Shanghai 200062
2. Dept of Endocrinolog, Putuo Hospital Affiliated to Shanghai University of Traditional Chinese Medicine , Shanghai 200062
3. School of Medical and Life Sciences , Chengdu University of Traditional Chinese Medicine , Chengdu 610000
- Publication Type:Journal Article
- Keywords:
glycated low density lipoprotein;
human umbilical vein endothelial cells;
TLR4;
HIF⁃1α
- From:
Acta Universitatis Medicinalis Anhui
2022;57(10):1614-1620
- CountryChina
- Language:Chinese
-
Abstract:
Objective :To investigate the effects of glycated low density lipoprotein (Gly⁃LDL) on the growth of human umbilical vein endothelial cells (HUVECs) and the expression of toll like receptor 4 (TLR4) and hypoxia inducible factor⁃1α (HIF⁃1α), and to explore its possible mechanism .
Methods :HUVECs were cultured in vitro and divided into control group, positive control group[50 mg/L normal low density lipoprotein(n⁃LDL)], low concentration, medium concentration and high concentration Gly⁃LDL(50, 75, 100 mg/L) groups . Respectively, the effects of different concentrations of Gly⁃LDL on survival rate of HUVECs were detected by CCK⁃8; The motility of HUVECs under different treatments were detected by wound healing assays; The level of inflammatory cytokine, such as tumor inducing factor⁃α(TNF⁃α), interleukin⁃6(IL⁃6), intercellular adhesion molecule⁃1(ICAM⁃1) and vascular cell adhesion molecule⁃1(VCAM⁃1) were detected by ELISA; The mRNA levels of TLR4, HIF⁃1α, TNF⁃α and IL⁃6 were detected by qRT⁃PCR; Protein expressions of TLR4, HIF⁃1α, TNF⁃α and IL⁃6 were detected by Western blot; Respectively, si⁃RNA of TLR4 and HIF⁃1α was used to intervene the effects of Gly⁃LDL on HUVECs . The experiment was divided into control group, model group (Gly⁃LDL 100 mg/L), si⁃TLR4 group (Gly⁃LDL 100 mg/L + si⁃TLR4), TLR4 unloading group( Gly⁃LDL 100 mg/L + si⁃NC1), si⁃HIF⁃1α group ( Gly⁃LDL 100 mg/L + si⁃HIF⁃1α) and HIF⁃1α unloading group ( Gly⁃LDL 100 mg/L + si⁃NC2) . Protein expressions of TLR4 and HIF⁃1α were detected by Western blot to verify the interaction between TLR4 and HIF⁃1α .
Results:The survival rate and migration rate of HUVECs were inhibited in Gly⁃LDL(50 mg/L, 75 mg/L, 100 mg/L) group (P < 0. 01), the inflammatory cytokines, such as TNF⁃α, IL⁃6, ICAM⁃1,VCAM⁃1 increased by Gly⁃LDL function on HUVECs(P < 0. 001), and the mRNA and protein levels of TLR4, HIF⁃1α, TNF⁃α and IL⁃6 increased by Gly⁃LDL in a dose dependent manner. After TLR4 was knocked out, the proteins expression of TLR4 and HIF⁃1α were down⁃regulated compared with model group(P < 0. 05),but after HIF⁃1α was knockout, only the protein expression of HIF⁃1α was down⁃regulated compared with model group( P < 0. 01),while the protein expression of TLR4 was up⁃regulated under the influence of Gly⁃LDL.
Conclusion : Gly⁃LDL may inhibit the proliferation and migration of HUVECs by up⁃regulating TLR4/HIF⁃1α inflammatory signaling pathway, and promote the expression of inflamma⁃tory cytokines, leading to vascular endothelial injury .
- Full text:2024081121275080812TLR4_HIF-1α信号...诱导的人脐静脉内皮细胞损伤_邱军辉.pdf