Abstract

BackgroundBrain iron is an essential as well as a toxic redox active element. Physiological levels are not uniform among the different cell types. Besides the availability of quantitative methods, the knowledge about the brain iron lags behind. Thereby, disclosing the mechanisms of brain iron homeostasis helps to understand pathological iron-accumulations in diseased and aged brains. With our study we want to contribute closing the gap by providing quantitative data on the concentration and distribution of iron in neurons and glial cells in situ. Using a nuclear microprobe and scanning proton induced X-ray emission spectrometry we performed quantitative elemental imaging on rat brain sections to analyze the iron concentrations of neurons and glial cells.ResultsNeurons were analyzed in the neocortex, subiculum, substantia nigra and deep cerebellar nuclei revealing an iron level between (0.53pm 2) and (0.68pm 2),upmu hbox {M}. The iron concentration of neocortical oligodendrocytes is fivefold higher, of microglia threefold higher and of astrocytes twofold higher compared to neurons. We also analyzed the distribution of subcellular iron concentrations in the cytoplasm, nucleus and nucleolus of neurons. The cytoplasm contains on average 73% of the total iron, the nucleolus—although a hot spot for iron—due to its small volume only 6% of total iron. Additionally, the iron level in subcellular fractions were measured revealing that the microsome fraction, which usually contains holo-ferritin, has the highest iron content. We also present an estimate of the cellular ferritin concentration calculating 133pm 25 ferritin molecules per upmu hbox {m} in rat neurons.ConclusionGlial cells are the most iron-rich cells in the brain. Imbalances in iron homeostasis that lead to neurodegeneration may not only be originate from neurons but also from glial cells. It is feasible to estimate the ferritin concentration based on measured iron concentrations and a reasonable assumptions on iron load in the brain.

Highlights

  • Brain iron is an essential as well as a toxic redox active element

  • Qualitative elemental analysis of subcellular fractions of brain homogenate Fractions enriched in subcellular organelles of neocortex were obtained by differential centrifugation

  • The differences among the brain regions and the cell types involved in each disorder makes it unlikely to succeed as a general strategy, and the cellular differences in iron concentrations and distributions presented in this study suggest differences in functionality and pathological potential

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Summary

Introduction

Brain iron is an essential as well as a toxic redox active element. Besides the availability of quantitative methods, the knowledge about the brain iron lags behind. Thereby, disclosing the mechanisms of brain iron homeostasis helps to understand pathological ironaccumulations in diseased and aged brains. With our study we want to contribute closing the gap by providing quantitative data on the concentration and distribution of iron in neurons and glial cells in situ. Using a nuclear microprobe and scanning proton induced X-ray emission spectrometry we performed quantitative elemental imaging on rat brain sections to analyze the iron concentrations of neurons and glial cells. No other organ than the brain constantly needs readily available iron in a regional, cellular and age sensitive manner [2]. Excessive free iron increases the risk to generate highly reactive radicals such as hydroxyl radical via the Fenton reaction.

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