Y. Sato et al., IMMUNOHISTOCHEMICAL LOCALIZATION OF FACILITATED-DIFFUSION GLUCOSE TRANSPORTERS IN RAT PANCREATIC-ISLETS, Tissue & cell, 28(6), 1996, pp. 637-643
The subcellular localization of five isoforms of facilitated-diffusion
glucose transporters (GLUTs), from GLUT1 to GLUT5, in rat pancreatic
islets was studied by immunohistochemistry using rabbit polyclonal ant
isera against mouse or rat GLUT peptides. Animals were perfusion-fixed
with phosphate-buffered 4% paraformaldehyde and the pancreases were r
emoved. Some specimens were embedded in paraffin, serially sectioned,
and immunostained for glucagon, insulin, somatostatin, and the GLUTs f
or light microscopic observation. Others were prepared for immunoelect
ron microscopy by the post-embedding method. By these methods, GLUT2 i
mmunostaining was observed on the lateral membranes of pancreatic beta
-cells, whereas GLUT3 immunoreaction was predominantly localized in th
e cytoplasm of beta-cells and was not found in alpha-cells. In contras
t, GLUT5 immunostaining was preferentially localized in the cytoplasm
of alpha-cells compared to that of beta-cells. However, GLUT1 and GLUT
4 were either barely or not at all detectable in any cells. These resu
lts suggest that rat islets take up glucose by at least three differen
t processes and that blood glucose levels could be modulated different
ially by: a high Km glucose transporter, GLUT2, in beta-cells; by a lo
w Km glucose transporter, GLUT3, in beta-cells; and by a low Km glucos
e transporter, GLUT5, in alpha-cells.