Role of Foxo6 in insulin resistance of vascular endothelial cells induced by high glucose and high fat and its interaction with NF-κB pathway
- Author:
Min XIA
1
;
Xiao-Wei XIONG
1
;
Ai-Lin NIU
1
;
Ting-Ting YIN
1
;
Ya-Nan ZHANG
1
;
Qi-Ren HUANG
1
;
Min XIA
2
;
Xiao-Wei XIONG
2
;
Ai-Lin NIU
2
;
Ting-Ting YIN
2
;
Ya-Nan ZHANG
2
;
Qi-Ren HUANG
2
;
Yi-Si TU
3
Author Information
- Publication Type:Journal Article
- Keywords: endothelial cells; forkhead box protein; hyperglycemia; hyperlipidemia; insulin resistance; NF-κBp65
- From: Chinese Pharmacological Bulletin 2022;38(4):552-561
- CountryChina
- Language:Chinese
- Abstract: Aim To investigate the expression of Foxos in human umbilical vein endothelial cells(HUVECs)with insulin resistance(IR)induced by high glucose and high fat(HG/HF)stress and its significance.Methods First, the IR model of endothelial cells was established by HG /HF stress.The differential expression of Foxos gene in normal(Ctrl )group and HG /HF group was observed, and the subtypes with the most significant changes in Foxos were screened out, such as Foxo6.Next, Foxo6 was silenced to observe its role in endothelial cell with IR.Finally, whether the mechanism of Foxo6-mediated IR was related to the interaction of NF-κB signaling was investigated.Results The expression increase of Foxo6 was the most significant among Foxos under the IR condition induced by HG/HF.Using a small RNA interference and plasmid transfection technique, we found that the silence effect of the siRNA3 fragments targeting Foxo6 was the most significant among the siRNAs.Moreover, the further study showed that silencing the Foxo6 gene could significantly reverse the endothelial IR induced by HG/HF, and the mechanism of the reversal effect was related to the interaction between the Foxo6 and NF-κB signal.Conclusions Foxo6 mediates the endothelial cell IR induced by the HG /HF stress.The underlying mechanism is that Foxo6 can interact with NF-κBp65 and activate NF-κB signaling pathway.Silencing Foxo6 can improve the IR of vascular endothelial cells induced by HG /HF stress.
