Transient Expression of Iron Transport Proteins in the Capillary of the Developing Rat Brain

• Published in: Cellular and molecular neurobiology Vol. 31; no. 1; pp. 93 - 99
• Main Authors: Yang, W. M, Jung, K. J, Lee, M. O, Lee, Y. S, Lee, Y. H, Nakagawa, S, Niwa, M, Cho, S. S, Kim, D. W
• Format: Journal Article
• Language: English
• Published: Boston Boston : Springer US 01.01.2011; Springer US
• Subjects: Animals; Animals, Newborn; Biomedical and Life Sciences; Biomedicine; Blood-Brain Barrier - metabolism; Brain - blood supply; Brain - growth & development; Brain - metabolism; Capillaries - metabolism; Carrier Proteins - genetics; Carrier Proteins - metabolism; Cation Transport Proteins - genetics; Cation Transport Proteins - metabolism; Cell Biology; Cells, Cultured; Endothelial Cells - metabolism; Gene Expression Regulation, Developmental; Hephaestin; Ion Transport - genetics; Iron - metabolism; Membrane Proteins - genetics; Membrane Proteins - metabolism; MTP-1 (ferroportin); Neurobiology; Neurosciences; Original Research; Pericyte; Rats; Rats, Sprague-Dawley; Receptors, Transferrin - genetics; Receptors, Transferrin - metabolism; Time Factors; transferrin; Transferrin - genetics; Transferrin - metabolism; Transferrin receptor; Hephaestin; Pericyte; Transferrin; MTP-1 (ferroportin); Transferrin receptor
• ISSN: 0272-4340; 1573-6830
• DOI: 10.1007/s10571-010-9558-0

Iron is essential for normal brain function and its uptake in the developing rat brain peaks during the first two weeks after birth, prior to the formation of the blood-brain barrier (BBB). The first step of iron transport from the blood to the brain is transferrin receptor (TfR)-mediated endocytosis in the capillary endothelial cells. However, the subsequent step from the endothelium into interstitium has not been fully described. The goal of this study was to examine the expression of iron transport proteins by immunodetection and RT-PCR in the developing rat brain. Tf and TfR are transiently expressed in perivascular NG2+ cells of the capillary wall during the early postnatal weeks in the rat brain. However, MTP-1 and hephaestin were expressed in endothelial cells, but not in the NG2+ perivascular cells. Immunoblot analysis for these iron transfer proteins in the developing brain generally confirmed the immunochemical findings. Furthermore, the expression of Tf and TfR in the blood vessels precedes its expression in oligodendrocytes, the main iron-storing cells in the vertebrate brain. RT-PCR analysis for the primary culture of endothelial cells and pericytes revealed that Tf and TfR were highly expressed in the pericytes while MTP-1 and hephaestin were expressed in the endothelial cells. The specific expression of Tf and TfR in brain perivascular cells and MTP-1 and hephaestin in endothelial cells suggest the possibility that trafficking of elemental iron through perivascular cells may be instrumental in the distribution of iron in the developing central nervous system.