Tumor necrosis factor alpha-induced glucose transporter (GLUT-1) mRNA stabilization in 3T3-L1 preadipocytes. Regulation by the adenosine-uridine binding factor.

Tumor necrosis factor alpha (TNF alpha), 12-O-tetradecanoylphorbol-13-acetate and cAMP stimulate hexose transport in quiescent 3T3-L1 preadipocytes by stabilizing the relatively labile mRNA coding for the basal glucose transporter, GLUT-1. The 3'-UTR of GLUT-1 mRNA contains a single copy of the destabilizing AUUUA motif in the context of an AU-rich region. The adenosine-uridine binding factor (AUBF) is a cytosolic protein which interacts with similar AU-rich regions in a variety of labile cytokine and oncogene mRNAs. Here, we demonstrate that AUBF complexes in vitro with GLUT-1 mRNA through the AU-rich portion of the 3'-UTR. AUBF activity is very low in quiescent preadipocytes, but can be up-regulated by agonists such as TPA, TNF alpha, cAMP, and okadaic acid, all of which stabilize GLUT-1 mRNA. The time courses of TNF alpha- and TPA-mediated AUBF up-regulation and GLUT-1 mRNA stabilization are coincident, suggesting a cause and effect relationship.     

Insulin responsiveness in skeletal muscle is determined by glucose transporter (Glut4) protein level.

Glucose transport in skeletal muscle is mediated by two distinct transporter isoforms, designated muscle/adipose glucose transporter (Glut4) and erythrocyte/HepG2/brain glucose transporter (Glut1), which differ in both abundance and membrane distribution. The present study was designed to investigate whether differences in insulin responsiveness of red and white muscle might be due to differential expression of the glucose transporter isoforms. Glucose transport, as well as Glut1 and Glut4 protein and mRNA levels, were determined in red and white portions of the quadriceps and gastrocnemius muscles of male Sprague-Dawley rats (body wt. approx. 250 g). Maximal glucose transport (in response to 100 nM-insulin) in the perfused hindlimb was 3.6 times greater in red than in white muscle. Red muscle contained approx. 5 times more total Glut4 protein and 2 times more Glut4 mRNA than white muscle, but there were no differences in the Glut1 protein or mRNA levels between the fibre types. Our data indicate that differences in responsiveness of glucose transport in specific skeletal muscle fibre types may be dependent upon the amount of Glut4 protein. Because this protein plays such an integral part in glucose transport in skeletal muscle, any impairment in its expression may play a role in insulin resistance.     

Mesure journaliére sur cycle végétatif complet des échanges gazeux: photosynthése, transpiration et respiration nocturne ďune culture de Maïs conduite sur colonnes de sol

Daily measurement of gas exchanges during a complete growth cycle: photosynthesis, transpiration and night respiration in a soil culture of maize. During a complete growth cycle, photosynthesis (P), night-respiration (R) and transpiration (T) have been measured daily for maize (Zea mays L. cv. INRA F7 × F2) in a self-regulating growth chamber. P and T varied according to three different kinetics. During the growing period there was a fast and concomitant variation of both P and T, which could be filled to a power function of time. During the fructification period we observed a linear decrease of P and T. Finally, during the senescence period P decreased to zero, whereas T kept a value higher than the evaporation of the naked soil. In the first two periods, the P/T ratio decreased as leaves aged. From this we could deduce that a slow increase of stomatal resistance (RS) and mesophyll resistance (RM) took place. R increased until the panicle appeared; it remained constant during fructification and then it decreased with senescence. Each nitrogen supply induced a transient increase of R. Finally, a water stress led to a greater decrease of P than of R, but the after effect of water stress disappeared a day later. These results were compared with those obtained in hydroponic conditions.