The retinal pigment epithelium (RPE) separates the outer retina from its bl
ood supply. To satisfy the retina's large requirement for glucose, the RPE
expresses high levels of glucose transporters. In most rat cells, the trans
porter GLUT3 provides a basal level of transport, but the expression of GLU
T1 can be regulated. The opposite is true in chicken (P. Wagstaff, H.Y. Kan
g, D. Mylott, P.J. Robbins, M.K. White, Characterization of the avian GLUT1
glucose transporter: differential regulation of GLUT1 and GLUT3 in chicken
embryo fibroblasts, Mel. Biol. Cell 6 (1995) 1575-1589). We examined chick
RPE to determine which isoform is regulated during development, and if the
neural retina regulates GLUT expression. By RT-PCR, RPE expressed GLUT1 an
d GLUT3, but not GLUT2. Only the level of GLUT1 increased between E5 and E1
8. A corresponding increase in GLUT1 protein was observed by immunoblotting
. Most of the increase occurred between E14 and E18, which corresponds to t
he late stage of tight junction development. A culture model of development
was used to examine the intermediate phase, which extends from E7 to E14.
While medium conditioned by the neural retina decreased paracellular diffus
ion across the tight junctions, it increased diffusion through the glucose
transporters. Unlike mammals, chick upregulates different isoforms in quies
cent RPE and proliferating fibroblasts. Further, the upregulation of glucos
e transport is coordinated with the development of tight junctions in the b
lood-retinal barrier. (C) 2000 Elsevier Science B.V. All rights reserved.