Functional Vitamin D Receptor (VDR) in the T-Tubules of Cardiac Myocytes: VDR Knockout Cardiomyocyte Contractility

• Published in: Endocrinology (Philadelphia) Vol. 149; no. 2; pp. 558 - 564
• Main Authors: Tishkoff, Daniel X, Nibbelink, Karl A, Holmberg, Kristina H, Dandu, Loredana, Simpson, Robert U
• Format: Journal Article
• Language: English
• Published: Bethesda, MD Endocrine Society 01.02.2008; The Endocrine Society
• Subjects: Animals; Biological and medical sciences; Calcitriol - metabolism; Female; Fundamental and applied biological sciences. Psychology; Mice; Mice, Knockout; Myocardial Contraction - physiology; Myocytes, Cardiac - physiology; Radioligand Assay; Rats; Rats, Sprague-Dawley; Receptors, Calcitriol - genetics; Receptors, Calcitriol - metabolism; Tritium; Vertebrates: endocrinology; Heart; Vitamin D receptor; Contractility; Circulatory system; Mutation; Heart cell; Myocyte
• ISSN: 0013-7227; 1945-7170
• DOI: 10.1210/en.2007-0805

We have previously shown that the active form of vitamin D, 1,25 dihydroxyvitamin D3 [1,25(OH)2D3], has both genomic and rapid nongenomic effects in heart cells; however, the subcellular localization of the vitamin D receptor (VDR) in heart has not been studied. Here we show that in adult rat cardiac myocytes the VDR is primarily localized to the t-tubule. Using immunofluorescence and Western blot analysis, we show that the VDR is closely associated with known t-tubule proteins. Radioligand binding assays using 3H-labeled 1,25(OH)2D3 demonstrate that a t-tubule membrane fraction isolated from homogenized rat ventricles contains a 1,25(OH)2D3-binding activity similar to the classic VDR. For the first time, we show that cardiac myocytes isolated from VDR knockout mice show accelerated rates of contraction and relaxation as compared with wild type and that 1,25(OH)2D3 directly affects contractility in the wild-type but not the knockout cardiac myocyte. Moreover, we observed that acute (5 min) exposure to 1,25(OH)2D3 altered the rate of relaxation. A receptor localized to t-tubules in the heart is ideally positioned to exert an immediate effect on signal transduction mediators and ion channels. This novel discovery is fundamentally important in understanding 1,25(OH)2D3 signal transduction in heart cells and provides further evidence that the VDR plays a role in heart structure and function.