Published online Nov 15, 2021. doi: 10.4239/wjd.v12.i11.1875
Peer-review started: May 26, 2021
First decision: June 16, 2021
Revised: June 29, 2021
Accepted: August 20, 2021
Article in press: August 20, 2021
Published online: November 15, 2021
Processing time: 173 Days and 6.6 Hours
The formation and accumulation of advanced glycation end products (AGEs) contribute to accelerated macrovascular complications, which are the leading cause of morbidity and mortality in patients with diabetes. Profilin-1 plays an important role in vascular remodeling and vascular inflammation.
Currently, few studies have investigated the role of profilin-1 in vasculopathy induced by AGEs, and the mechanism of profilin-1 in diabetic macroangiopathy remains unclear.
The aim of this study was to explore the potential role of profilin-1 in the pathogenesis of atherosclerosis induced by AGEs and to elucidate its probable mechanism.
Eighty-nine individuals undergoing coronary angiography were enrolled in the study. Plasma cytokine levels were detected using ELISA kits. Rat aortic vascular smooth muscle cells were incubated with different compounds for different times. Cell proliferation was determined by performing the MTT assay and EdU staining. An AGEs-induced vascular remodeling model was established in rats and histological and immunohistochemical analyses were performed. The mRNA and protein levels were detected using real-time PCR and Western blot analysis, respectively. In vivo, shRNA transfection was performed to verify the role of profilin-1 in AGEs-induced proatherogenic mediator release and aortic remodeling. Statistical analyses were performed using SPSS 22.0 software.
Compared with the control group, plasma levels of profilin-1 and receptor for AGEs (RAGE) were significantly increased in patients with coronary artery disease, especially in those complicated with diabetes mellitus (P < 0.01). The levels of profilin-1 were positively correlated with the levels of RAGE (P < 0.01); additionally, the levels of both molecules were positively associated with the degree of coronary artery stenosis (P < 0.01). In vivo, tail vein injections of AGEs induced the release of proatherogenic mediators, such as asymmetric dimethylarginine, intercellular adhesion molecule-1, and the N-terminus of procollagen III peptide, concomitant with apparent aortic morphological changes and significantly upregulated expression of the profilin-1 mRNA and protein in the thoracic aorta (P < 0.05 and P < 0.01). Downregulation of profilin-1 expression with an shRNA significantly attenuated AGEs-induced proatherogenic mediator release (P < 0.05) and aortic remodeling. In vitro, incubation of vascular smooth muscle cells (VSMCs) with AGEs significantly promoted cell proliferation and upregulated the expression of the profilin-1 mRNA and protein (P < 0.05). AGEs (200 μg/mL, 24 h) significantly upregulated the expression of the signal transducer and activator of transcription 3 (STAT3) mRNA and protein and the Janus kinase 2 (JAK2) protein, which were blocked by a JAK2 inhibitor (T3042-1) and/or STAT3 inhibitor (T6308-1) (P < 0.05). In addition, pretreatment with T3042-1 or T6308-1 significantly inhibited AGEs-induced rat aortic vascular smooth muscle cell proliferation (P < 0.05).
The present study proved that AGEs induce proatherogenic events such as VSMC proliferation, proatherogenic mediator expression, and vascular remodeling, which are attenuated by silencing profilin-1 gene expression.
Profilin-1 is expected to be a promising therapeutic target for the prevention of diabetes mellitus associated with vascular damage. Further studies are needed to develop a targeted drug against profilin-1 and elucidate the exact molecular mechanism of profilin-1 in AGEs-induced vasculopathy.