1,25 Dihydroxyvitamin D3 Inhibits TGFβ1-Mediated Primary Human Cardiac Myofibroblast Activation

Aims Epidemiological and interventional studies have suggested a protective role for vitamin D in cardiovascular disease, and basic research has implicated vitamin D as a potential inhibitor of fibrosis in a number of organ systems; yet little is known regarding direct effects of vitamin D on human cardiac cells. Given the critical role of fibrotic responses in end stage cardiac disease, we examined the effect of active vitamin D treatment on fibrotic responses in primary human adult ventricular cardiac fibroblasts (HCF-av), and investigated the relationship between circulating vitamin D (25(OH)D 3 ) and cardiac fibrosis in human myocardial samples. Methods and Results Interstitial cardiac fibrosis in end stage HF was evaluated by image analysis of picrosirius red stained myocardial sections. Serum 25(OH)D 3 levels were assayed using mass spectrometry. Commercially available HCF-av were treated with transforming growth factor (TGF)β 1 to induce activation, in the presence or absence of active vitamin D (1,25(OH) 2 D 3 ). Functional responses of fibroblasts were analyzed by in vitro collagen gel contraction assay. 1,25(OH) 2 D 3 treatment significantly inhibited TGFβ 1 -mediated cell contraction, and confocal imaging demonstrated reduced stress fiber formation in the presence of 1,25(OH) 2 D 3 . Treatment with 1,25(OH) 2 D 3 reduced alpha-smooth muscle actin expression to control levels and inhibited SMAD2 phosphorylation. Conclusions Our results demonstrate that active vitamin D can prevent TGFβ1-mediated biochemical and functional pro-fibrotic changes in human primary cardiac fibroblasts. An inverse relationship between vitamin D status and cardiac fibrosis in end stage heart failure was observed. Collectively, our data support an inhibitory role for vitamin D in cardiac fibrosis.