Abstract
BackgroundSmooth muscle cells play an important role in the development of atherosclerosis. SHP2 is known to regulate the proliferation and migration of smooth muscle cells. The purpose of this study was to determine whether the SHP2 inhibitor PHPS1 has a pro-atherosclerotic or an atheroprotective effect in vivo and in vitro.MethodsAfter exposure to a high-cholesterol diet for 4 weeks, LDL receptor-deficient (Ldlr−/−) mice were exposed to the SHP2 inhibitor PHPS1 or vehicle. Body weight, serum glucose and lipid levels were determined. The size and composition of atherosclerotic plaques were measured by en face analysis, Movat staining and immunohistochemistry. The phosphorylation of SHP2 and related signaling molecules was analyzed by Western blot. Mechanistic analyses were performed in oxLDL-stimulated cultured vascular smooth muscle cells (VSMCs) with or without 10 mM PHPS1 pretreatment. Protein phosphorylation levels were detected by Western blot, and VSMC proliferation was assessed by BrdU staining.ResultsPHPS1 decreased the number of atherosclerotic plaques without significantly affecting body weight, serum glucose levels or lipid metabolism. Plaque composition analysis showed a significant decrease in the number of VSMCs in atherosclerotic lesions of Ldlr−/− mice treated with PHPS1. Stimulation with oxLDL induced a dose-dependent increase in the number of VSMCs and in SHP2 and ERK phosphorylation levels, and these effects were blocked by PHPS1.ConclusionThe SHP2 inhibitor PHPS1 exerts a protective effect against atherosclerosis by reducing VSMC proliferation via SHP2/ERK pathway activation.
Highlights
Smooth muscle cells play an important role in the development of atherosclerosis
No significant differences in body weight or the levels of serum glucose, total cholesterol (TC), TG, high-density lipoprotein cholesterol (HDL-C) or lowdensity lipoprotein cholesterol (LDL-C) were observed among the three groups (Additional file 1: Figure S1)
This study showed that inhibiting the tyrosine phosphatase SHP2 with phenylhydrazono pyrazolone sulfonate 1 (PHPS1) prevented the development of AS by inhibiting vascular smooth muscle cells (VSMCs) proliferation
Summary
Smooth muscle cells play an important role in the development of atherosclerosis. SHP2 is known to regulate the proliferation and migration of smooth muscle cells. Protein phosphorylation levels were detected by Western blot, and VSMC proliferation was assessed by BrdU staining. Src homology 2 domain-containing protein tyrosine phosphatase 2 (SHP2), known as protein tyrosine phosphatase N 11 (PTPN11), is an important PTP that acts downstream of various growth factors, cytokines and tyrosine kinases. It plays an integral role in multiple cellular
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