Structural-functional analysis of diffusion in glucose absorption by rat small intestine enterocytes

• Published in: T͡S︡itologii͡a Vol. 48; no. 4; p. 355
• Main Authors: Grefner, N M, Gromova, L V, Gruzdkov, A A, Snigirevskaia, E S, Komissarchik, Ia Iu
• Format: Journal Article
• Language: Russian
• Published: Russia (Federation) 2006
• Subjects: Animals; Biological Transport; Desmosomes - metabolism; Desmosomes - ultrastructure; Diffusion; Enterocytes - metabolism; Enterocytes - ultrastructure; Glucose - metabolism; Glucose Transporter Type 2 - metabolism; Immunohistochemistry; Intestinal Absorption; Intestine, Small - metabolism; Intestine, Small - ultrastructure; Microscopy, Confocal; Microscopy, Electron, Transmission; Protein Kinase C - metabolism; Protein Kinase C beta; Rats; Rats, Wistar; Tight Junctions - metabolism; Tight Junctions - ultrastructure
• ISSN: 0041-3771

To elucidate mechanisms providing transport of sugars across intestinal epithelium, on taking into account the current hypotheses (active transport, participation of paracellular transport and passive component of transcellular transport), it was important to reveal structural changes of tight junctions and distribution of the carriers of facilitated diffusion of GLUT2 and protein kinase C during absorption of glucose. On using confocal and electron microscopy, ultrastructural and immunocytochemical studies of enterocytes after perfusion of isolated rat small intestine fragment with 75 mM glucose (chronic experiment) have shown: 1) fluorescent labels of transporter GLUT2 and PKCbetaII are located in the apical area of enterocytes situated at the upper half of the villus. Antibodies against GLUT2, conjugated with gold, are revealed at the microvilli or apical membrane and in the area of terminal network; 2) no ultrastructural changes of the tight junction are detected on ultrathin sections and freeze--fracture replics. At the same time, fluorescent and gold labels against actin are concentrated in the vicinity of the lateral membrane in the tight junction area. The results obtained can serve a confirmation of a hypothesis that at high glucose concentrations GLUT2 participates in its transfer across the apical membrane.