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http://purl.uniprot.org/citations/37633478http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/37633478http://www.w3.org/2000/01/rdf-schema#comment"

Objective

The objective of this study is to determine how Musashi-2 (MSI2) affects vascular smooth muscle cell (VSMC) phenotypic switch and contributes to atherosclerosis (AS).

Methods

Primary mouse VSMCs were transfected with MSI2 specific siRNA and treated with platelet-derived growth factor-BB (PDGF-BB). The proliferation, cell-cycle, and migration of VSMCs were determined by CCK-8, flow cytometry, wound healing, and transwell assays. Western blot and qRT-PCR were conducted to analyze the protein and mRNA expression. Moreover, the correlation between MSI2, Fbxo6, Rnaset2, and chemokine signaling was predicted and verified using RNAct database, KEGG, wiki, RNA-binding protein immunoprecipitation and co-immunoprecipitation. Moreover, H&E and Oil Red O staining were employed for assessing necrotic core and lipid accumulation in AS mouse aorta tissues. The numbers of B lymphocytes and monocytes, and the levels of triglyceride (TG), total cholesterol (TC), high-density lipoprotein cholesterol (HDLC), and low-density lipoprotein cholesterol (LDL-C) in AS mice blood were investigated using flow cytometry and corresponding commercial kits, respectively.

Results

MSI2 was up-regulated in the PDGF-BB-treated VSMCs. Knockdown of MSI2 inhibited VSMC proliferation, cell-cycle, and migration. Moreover, MSI2 regulated VSMC phenotypic switch through binding with Fbxo6 to induce Rnaset2 ubiquitination. MSI2 knockdown inhibited chemokine signaling via regulating Fbxo6/Rnaset2 axis. In AS mice, knockdown of MSI2 inhibited the formation of necrotic core and atherosclerotic plaque, and inhibited chemokine signaling via regulating Fbxo6/Rnaset2 axis.

Conclusion

Our findings demonstrated that MSI2 could bind with Fbxo6 to induce Rnaset2 ubiquitination and the activation of chemokine signaling pathway during VSMC phenotypic switch in AS."xsd:string
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http://purl.uniprot.org/citations/37633478http://purl.uniprot.org/core/author"Li J."xsd:string
http://purl.uniprot.org/citations/37633478http://purl.uniprot.org/core/author"Wang M."xsd:string
http://purl.uniprot.org/citations/37633478http://purl.uniprot.org/core/author"Zhang T."xsd:string
http://purl.uniprot.org/citations/37633478http://purl.uniprot.org/core/author"Zhang S."xsd:string
http://purl.uniprot.org/citations/37633478http://purl.uniprot.org/core/author"Wu S."xsd:string
http://purl.uniprot.org/citations/37633478http://purl.uniprot.org/core/author"Xu R."xsd:string
http://purl.uniprot.org/citations/37633478http://purl.uniprot.org/core/date"2023"xsd:gYear
http://purl.uniprot.org/citations/37633478http://purl.uniprot.org/core/name"Cell Signal"xsd:string
http://purl.uniprot.org/citations/37633478http://purl.uniprot.org/core/pages"110869"xsd:string
http://purl.uniprot.org/citations/37633478http://purl.uniprot.org/core/title"Musashi-2 binds with Fbxo6 to induce Rnaset2 ubiquitination and chemokine signaling pathway during vascular smooth muscle cell phenotypic switch in atherosclerosis."xsd:string
http://purl.uniprot.org/citations/37633478http://purl.uniprot.org/core/volume"111"xsd:string
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