The first planet detected in the WTS: an inflated hot-Jupiter in a 3.35 d orbit around a late F star [Erratum]

We report the discovery of WTS-1b, the first extrasolar planet found by the WFCAM Transit Survey, which began observations at the 3.8-m United Kingdom Infrared Telescope (UKIRT) in August 2007. Light curves comprising almost 1200 epochs with a photometric precision of better than 1 per cent to J ~ 16 were constructed for ~60000 stars and searched for periodic transit signals. For one of the most promising transiting candidates, high-resolution spectra taken at the Hobby-Eberly Telescope (HET) allowed us to estimate the spectroscopic parameters of the host star, a late-F main sequence dwarf (V=16.13) with possibly slightly subsolar metallicity, and to measure its radial velocity variations. The combined analysis of the light curves and spectroscopic data resulted in an orbital period of the substellar companion of 3.35 days, a planetary mass of 4.01 +- 0.35 Mj and a planetary radius of 1.49+0.16-0.18 Rj. WTS-1b has one of the largest radius anomalies among the known hot Jupiters in the mass range 3-5 Mj. The high irradiation from the host star ranks the planet in the pM class.Comment: 16 pages, 10 figure

Subcellular trafficking of the substrate transporters GLUT4 and CD36 in cardiomyocytes

Cardiomyocytes use glucose as well as fatty acids for ATP production. These substrates are transported into the cell by glucose transporter 4 (GLUT4) and the fatty acid transporter CD36. Besides being located at the sarcolemma, GLUT4 and CD36 are stored in intracellular compartments. Raised plasma insulin concentrations and increased cardiac work will stimulate GLUT4 as well as CD36 to translocate to the sarcolemma. As so far studied, signaling pathways that regulate GLUT4 translocation similarly affect CD36 translocation. During the development of insulin resistance and type 2 diabetes, CD36 becomes permanently localized at the sarcolemma, whereas GLUT4 internalizes. This juxtaposed positioning of GLUT4 and CD36 is important for aberrant substrate uptake in the diabetic heart: chronically increased fatty acid uptake at the expense of glucose. To explain the differences in subcellular localization of GLUT4 and CD36 in type 2 diabetes, recent research has focused on the role of proteins involved in trafficking of cargo between subcellular compartments. Several of these proteins appear to be similarly involved in both GLUT4 and CD36 translocation. Others, however, have different roles in either GLUT4 or CD36 translocation. These trafficking components, which are differently involved in GLUT4 or CD36 translocation, may be considered novel targets for the development of therapies to restore the imbalanced substrate utilization that occurs in obesity, insulin resistance and diabetic cardiomyopathy