Evidence map›Paper›PMID 41889472›Full record

ArticleChemical & biomedical imaging2026

Integrating Microscopy Methods to Study Gene and Protein Expression alongside Metal Ion Distribution and Speciation: A Case Study of Iron within Pyramidal Neurons from Distinct Hippocampal CA1 Subregions.

Gaewyn Ellison, Rhiannon E Boseley, Meg Willans, Sarah Williams, Evelyn S Innes, Paige Barnard, Julia Koehn, Somayra S A Mamsa, Paul Quinn, Daryl L Howard and 2 more

Abstract read
In one paragraph

Article in Chemical & biomedical imaging, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Bioimaging of Metals.Chemical & biomedical imaging · 2026
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Gaewyn EllisonSchool of Molecular and Life Sciences, Faculty of Science and Engineering, Curtin University, Bentley, Perth, WA 6102, Australia.ORCID https://orcid.org/0000-0002-5382-4519
Rhiannon E BoseleyDiamond Light Source Ltd., Harwell Science and Innovation Campus, Didcot, Oxfordshire OX11 0DE, United Kingdom.ORCID https://orcid.org/0000-0002-7919-9977
Meg WillansSchool of Molecular and Life Sciences, Faculty of Science and Engineering, Curtin University, Bentley, Perth, WA 6102, Australia.ORCID https://orcid.org/0000-0001-6882-934X
Sarah WilliamsSchool of Molecular and Life Sciences, Faculty of Science and Engineering, Curtin University, Bentley, Perth, WA 6102, Australia.
Evelyn S InnesSchool of Molecular and Life Sciences, Faculty of Science and Engineering, Curtin University, Bentley, Perth, WA 6102, Australia.
Paige BarnardSchool of Molecular and Life Sciences, Faculty of Science and Engineering, Curtin University, Bentley, Perth, WA 6102, Australia.
Julia KoehnCurtin Medical Research Institute, Curtin University, Bentley, Perth, WA 6102, Australia.
Somayra S A MamsaCurtin Medical Research Institute, Curtin University, Bentley, Perth, WA 6102, Australia.
Paul QuinnDiamond Light Source, Harwell Science and Innovation Campus, Didcot, Oxfordshire OX11 0DE, United Kingdom.ORCID https://orcid.org/0000-0002-7607-4271
Daryl L HowardAustralian Synchrotron, ANSTO, Clayton, VIC 3168, Australia.
Simon A JamesAustralian Synchrotron, ANSTO, Clayton, VIC 3168, Australia.
Mark J HackettSchool of Molecular and Life Sciences, Faculty of Science and Engineering, Curtin University, Bentley, Perth, WA 6102, Australia.ORCID https://orcid.org/0000-0002-3296-7270

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Understanding the role of metal ions in normal and abnormal cell function continues to emerge as a critical research area in the biological and biochemical sciences. This is especially true in the context of brain health and neurodegenerative diseases, as the brain is especially enriched in metal ions. A range of microscopy and bioanalytical techniques are available to assist in characterizing and observing changes to the brain metallome. As is the case in many other scientific fields, the integration of multiple analytical methods often yields a more complete chemical picture and deeper biological understanding. Herein, we present a case study applying 4 different analytical methods to provide spatially resolved characterization of chemical and biochemical parameters relating to the iron (Fe) metallome within a specific brain region, cornu ammonis sector 1 (CA1) of the hippocampus. The CA1 hippocampal sector was chosen for investigation due to its known endogenous enrichment in Fe and its selective vulnerability to neurodegeneration. The 4 analytical techniques applied were X-ray fluorescence microscopy (to quantify Fe distribution); X-ray absorption near-edge structure (XANES) spectroscopy to reveal information on Fe oxidation state and coordination environment; immuno-fluorescence to reveal relative abundance of Fe storage proteins (heavy chain ferritin and mitochondrial ferritin); and spatial transcriptomics to reveal gene expression pathways relevant to Fe homeostasis. Collectively, the results highlight that although pyramidal neurons in lateral and medial regions of the hippocampal CA1 sector are morphologically similar, key differences in the Fe metallome are evident. The observed differences within the hippocampal CA1 sector potentially indicate a higher oxidative environment and higher metabolic turnover in medial CA1 neurons relative to lateral CA1 neurons, which may account for the heightened vulnerability to neurodegeneration that is observed in the medial CA1 sector.

Indexed as

brainCNSmemorymetallomicsneuorimagingneurodegeneration

Identifiers

PMID41889472
PMCPMC13014334

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.