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发育期大鼠脑毛细血管中铁转运蛋白的瞬时表达。

Transient expression of iron transport proteins in the capillary of the developing rat brain.

机构信息

Department of Anatomy, Research Institute for Medical Sciences, Chungnam National University School of Medicine, Daejeon, South Korea.

出版信息

Cell Mol Neurobiol. 2011 Jan;31(1):93-9. doi: 10.1007/s10571-010-9558-0.

Abstract

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.

摘要

铁对于正常的大脑功能是必不可少的,其在发育中的大鼠大脑中的摄取在出生后两周内达到峰值,此时血脑屏障(BBB)尚未形成。铁从血液到大脑的第一步是在毛细血管内皮细胞中通过转铁蛋白受体(TfR)介导的内吞作用。然而,从内皮细胞到间质的后续步骤尚未完全描述。本研究的目的是通过免疫检测和 RT-PCR 检查发育中大鼠脑中铁转运蛋白的表达。Tf 和 TfR 在大鼠脑出生后早期的周期间在血管周 NG2+细胞中短暂表达。然而,MTP-1 和 hephaestin 在内皮细胞中表达,但不在 NG2+血管周细胞中表达。在发育中的大脑中,这些铁转运蛋白的免疫印迹分析一般证实了免疫化学发现。此外,Tf 和 TfR 在血管中的表达先于其在少突胶质细胞中的表达,少突胶质细胞是脊椎动物大脑中主要的铁储存细胞。内皮细胞和周细胞的原代培养的 RT-PCR 分析表明,Tf 和 TfR 在周细胞中高度表达,而 MTP-1 和 hephaestin 在内皮细胞中表达。Tf 和 TfR 在脑血管周细胞中的特异性表达以及 MTP-1 和 hephaestin 在血管内皮细胞中的表达表明,通过血管周细胞运输元素铁可能有助于铁在发育中的中枢神经系统中的分布。

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