CCN5 knockout mice exhibit lipotoxic cardiomyopathy with mild obesity and diabetes.
Jihwa KimSanghyun JooGwang Hyeon EomSeung Hoon LeeMin-Ah LeeMiyoung LeeKi Woo KimDo Han KimHyun KookTae Hwan KwakWoo Jin ParkPublished in: PloS one (2018)
Obesity is associated with various human disorders, such as type 2 diabetes, cardiovascular diseases, hypertension, and cancers. In this study, we observed that knockout (KO) of CCN5, which encodes a matricellular protein, caused mild obesity in mice. The CCN5 KO mice also exhibited mild diabetes characterized by high fasting glucose levels and impaired insulin and glucose tolerances. Cardiac hypertrophy, ectopic lipid accumulation, and impaired lipid metabolism in hearts were observed in the CCN5 KO mice, as determined using histology, quantitative RT-PCR, and western blotting. Fibrosis was significantly greater in hearts from the CCN5 KO mice both in interstitial and perivascular regions, which was accompanied by higher expression of pro-fibrotic and pro-inflammatory genes. Both systolic and diastolic functions were significantly impaired in hearts from the CCN5 KO mice, as assessed using echocardiography. Taken together, these results indicate that CCN5 KO leads to lipotoxic cardiomyopathy with mild obesity and diabetes in mice.
Keyphrases
- high fat diet induced
- type diabetes
- insulin resistance
- cardiovascular disease
- glycemic control
- metabolic syndrome
- weight loss
- blood pressure
- left ventricular
- heart failure
- weight gain
- wild type
- adipose tissue
- gene expression
- transcription factor
- computed tomography
- physical activity
- coronary artery disease
- genome wide
- atrial fibrillation
- cardiovascular risk factors
- ejection fraction