Back to Search
Start Over
Regulation of Vascular Smooth Muscle Cell Dysfunction Under Diabetic Conditions by miR-504.
- Source :
-
Arteriosclerosis, thrombosis, and vascular biology [Arterioscler Thromb Vasc Biol] 2016 May; Vol. 36 (5), pp. 864-73. Date of Electronic Publication: 2016 Mar 03. - Publication Year :
- 2016
-
Abstract
- Objective: Diabetes mellitus accelerates proatherogenic and proinflammatory phenotype of vascular smooth muscle cell (VSMC) associated with vascular complications. Evidence shows that microRNAs (miRNAs) play key roles in VSMC functions, but their role under diabetic conditions is unclear. We profiled miRNAs in VSMC from diabetic mice and examined their role in VSMC dysfunction.<br />Approach and Results: High throughput small RNA-sequencing identified 135 differentially expressed miRNAs in VSMC from type 2 diabetic db/db mice (db/dbVSMC) versus nondiabetic db/+ mice. Several of these miRNAs were known to regulate VSMC functions. We further focused on miR-504, because it was highly upregulated in db/dbVSMC, and its function in VSMC is unknown. miR-504 and its host gene Fgf13 were significantly increased in db/dbVSMC and in aortas from db/db mice. Bioinformatics analysis predicted that miR-504 targets including signaling adaptor Grb10 and transcription factor Egr2 could regulate growth factor signaling. We experimentally validated Grb10 and Egr2 as novel targets of miR-504. Overexpression of miR-504 in VSMC inhibited contractile genes and enhanced extracellular signal-regulated kinase 1/2 activation, proliferation, and migration. These effects were blocked by miR-504 inhibitors. Grb10 knockdown mimicked miR-504 functions and increased inflammatory genes. Egr2 knockdown-inhibited anti-inflammatory Socs1 and increased proinflammatory genes. Furthermore, high glucose and palmitic acid upregulated miR-504 and inflammatory genes, but downregulated Grb10.<br />Conclusions: Diabetes mellitus misregulates several miRNAs including miR-504 that can promote VSMC dysfunction. Because changes in many of these miRNAs are sustained in diabetic VSMC even after in vitro culture, they may be involved in metabolic memory of vascular complications. Targeting such mechanisms could offer novel therapeutic strategies for diabetic complications.<br /> (© 2016 American Heart Association, Inc.)
- Subjects :
- Animals
Aorta, Thoracic metabolism
Aorta, Thoracic pathology
Aortic Diseases genetics
Aortic Diseases pathology
Atherosclerosis genetics
Atherosclerosis pathology
Cell Movement
Cell Proliferation
Cells, Cultured
Computational Biology
Diabetes Mellitus, Type 2 genetics
Diabetes Mellitus, Type 2 pathology
Diabetic Angiopathies genetics
Diabetic Angiopathies pathology
Disease Models, Animal
Early Growth Response Protein 2 genetics
Early Growth Response Protein 2 metabolism
Extracellular Signal-Regulated MAP Kinases metabolism
Fibroblast Growth Factors genetics
Fibroblast Growth Factors metabolism
GRB10 Adaptor Protein genetics
GRB10 Adaptor Protein metabolism
Gene Expression Profiling methods
Gene Expression Regulation
Glucose pharmacology
High-Throughput Nucleotide Sequencing
Male
MicroRNAs genetics
Muscle, Smooth, Vascular drug effects
Muscle, Smooth, Vascular pathology
Myocytes, Smooth Muscle drug effects
Myocytes, Smooth Muscle pathology
Palmitic Acid pharmacology
Phenotype
RNA Interference
Signal Transduction
Suppressor of Cytokine Signaling 1 Protein genetics
Suppressor of Cytokine Signaling 1 Protein metabolism
Transfection
Aortic Diseases metabolism
Atherosclerosis metabolism
Diabetes Mellitus, Type 2 metabolism
Diabetic Angiopathies metabolism
MicroRNAs metabolism
Muscle, Smooth, Vascular metabolism
Myocytes, Smooth Muscle metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1524-4636
- Volume :
- 36
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Arteriosclerosis, thrombosis, and vascular biology
- Publication Type :
- Academic Journal
- Accession number :
- 26941017
- Full Text :
- https://doi.org/10.1161/ATVBAHA.115.306770