Abstract

BackgroundIron transport across the blood-brain barrier (BBB) involves the cooperation of brain microvascular endothelial cells (BMVEC) and their neighboring astrocytes. Astrocytes secrete a soluble form of ceruloplasmin (sCp) which, in turn, acts to export iron from ferroportin (Fpn) on the basolateral surface of BMVEC. Although regulation of astrocyte sCp gene expression has been demonstrated to be influenced by interleukin-1 beta (IL-1β) and interleukin-6 (IL-6), the role of neighboring BMVEC in this regulation has yet to be determined and is the basis for this work.ResultsWe provide evidence that human BMVEC (hBMVEC) IL-1β and IL-6 positively influence the expression of sCp transcript by neighboring C6 glioma cells (astrocytes). The effect of hBMVEC on C6 glioma sCp expression at the level of transcript and protein was repressed via the addition of IL-1β and IL-6 pathway inhibitors (IL-1 receptor antagonist protein and SC144, respectively). Stimulation of hBMVEC interleukin gene expression by apical exposure to bacterial endotoxin lipopolysaccharide significantly enhanced hBMVEC-mediated C6 glioma sCp gene expression.ConclusionhBMVEC influence the gene expression of neighboring C6 glioma sCp. This change in gene expression is mediated by the secretion of IL-1β and IL-6 from hBMVEC. Furthermore, the hBMVEC-induced increase in neighboring C6 glioma sCp gene expression leads to an increased rate of hBMVEC iron efflux. Taken together, our results indicate that hBMVEC-secreted cytokine activity increases the gene expression of neighboring C6 glioma sCp, which reciprocally acts on basolateral hBMVEC Fpn to enhance brain iron import.

Highlights

  • Iron, a first-row transition metal, is essential for cellular respiration [1,2]

  • Results human BMVEC (hBMVEC) increase C6 glioma ceruloplasmin mRNA abundance We have demonstrated previously that C6 glioma cells grown distal to hBMVEC in a transwell culture system significantly enhance hBMVEC iron efflux into the basal chamber via secretion of C6 cell soluble form of ceruloplasmin (sCp) [7]

  • IL-1β and IL-6 act additively to increase C6 glioma sCp mRNA and protein Since both IL-1β and IL-6 are secreted from the basolateral surface of hBMVEC, we examined the direct effect of added recombinant cytokine on C6 glioma sCp abundance

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Summary

Introduction

A first-row transition metal, is essential for cellular respiration [1,2]. As the major user of metabolic energy (on a per-weight basis) the central nervous system (CNS) strongly relies on iron while at the same time is highly vulnerable to iron-induced oxidative stress. The export of iron from the basolateral surface of the brain microvascular endothelial cells (BMVEC) of the blood–brain barrier (BBB) is mediated by several different layers of regulation by neighboring astrocytes [7]. C6 cells increase the export of iron from the basolateral surface of BMVEC (and import into brain) via the secretion of the soluble multicopper oxidase ceruloplasmin (sCp) [7,10]. Iron transport across the blood–brain barrier (BBB) involves the cooperation of brain microvascular endothelial cells (BMVEC) and their neighboring astrocytes. Astrocytes secrete a soluble form of ceruloplasmin (sCp) which, in turn, acts to export iron from ferroportin (Fpn) on the basolateral surface of BMVEC. Regulation of astrocyte sCp gene expression has been demonstrated to be influenced by interleukin-1 beta (IL-1β) and interleukin-6 (IL-6), the role of neighboring BMVEC in this regulation has yet to be determined and is the basis for this work

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