Evidence map›Paper›PMID 39805676›Full record

ArticleJournal of clinical pathology2025

Single-molecule localisation microscopy (SMLM) is feasible in human and animal formalin fixed paraffin embedded (FFPE) tissues in medical renal disease.

Scarlet F Brockmoeller, Hayley Slaney, Alistair Curd, Aurora Bono, James H Felce, Deep Arora, Andrew Lewington, Andras G Miklosi, Philip Quirke

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Article in Journal of clinical pathology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Scarlet F BrockmoellerPathology & Data Analytics, Leeds Institute of Medical Research at St. James's, School of Medicine, University of Leeds, Leeds, LS9 7TF, UK S.F.Brockmoeller@leeds.ac.uk.ORCID http://orcid.org/0000-0002-7452-5833
Hayley SlaneyPathology & Data Analytics, Leeds Institute of Medical Research at St. James's, School of Medicine, University of Leeds, Leeds, LS9 7TF, UK.
Alistair CurdPathology & Data Analytics, Leeds Institute of Medical Research at St. James's, School of Medicine, University of Leeds, Leeds, LS9 7TF, UK.
Aurora BonoPathology & Data Analytics, Leeds Institute of Medical Research at St. James's, School of Medicine, University of Leeds, Leeds, LS9 7TF, UK.
James H FelceONI UK, Linacre House, Banbury Road, Oxford, OX2 8TA, UK.
Deep AroraDepartment of Histopathology, Bexley Wing, Level 5, St James's University Hospital, Leeds, LS9 7TF, UK.
Andrew LewingtonRenal Department, St. James's University Hospital, Leeds, LS9 7TF, UK.
Andras G MiklosiONI UK, Linacre House, Banbury Road, Oxford, OX2 8TA, UK.
Philip QuirkePathology & Data Analytics, Leeds Institute of Medical Research at St. James's, School of Medicine, University of Leeds, Leeds, LS9 7TF, UK.

Funding

Wellcome Trust
6 · The paper itself

Abstract

aimsEstablishment of a protocol for routine single-molecule localisation microscopy (SMLM) imaging on formalin fixed paraffin embedded (FFPE) tissue using medical renal disease including minimal change disease (MCD) and focal segmental glomerulosclerosis (FSGS).

methodsProtocol for normal and diseased renal FFPE tissue was developed to investigate the clinical diagnostic potential of SMLM. Antibody concentrations were determined for confocal microscopy and transferred to SMLM. Different fixatives and lengths of fixation were studied. To reduce autofluorescence, additional quenching and UV bleaching steps were compared. Optimal SMLM acquisition settings were established. SMLM data were imaged, digitally captured, stored, visually inspected and analysed quantitatively.

resultsProtocol was established on normal renal FFPE tissue and then applied to clinical diseased tissue with single and multiple markers. Antibodies against key diagnostic proteins including podocin, nephrin, collagen, laminin, synaptopodin, CD31, IgG, IgM and IgA antibodies were established for MCD, FSGS and immune-mediated renal disease. We found important characteristic differences in the renal diseases listed above.

conclusionsWe established a routine super-resolution microscopy protocol for clinical FFPE material on medical renal biopsies, which could visualise fluorescently labelled proteins in all glomeruli present with a precision of approximately 10-20 nm, with a turnaround under 48 hours. We visualised and quantitated specific protein distributions in different conditions. SMLM opens subcellular microscopy in FFPE to histopathologists on routine FFPE tissue, which can in the future be an adjunct and, in some aspects, a rapid superior alternative to electron microscopy.

Indexed as

Glomerulosclerosis, Focal SegmentalKidneyKidney DiseasesNephrosis, LipoidSingle Molecule ImagingAnimalsBiomarkersBiopsyFeasibility StudiesFixativesFormaldehydeHumansMicroscopy, ConfocalParaffin EmbeddingTissue FixationBiomarkersFixativesFormaldehydeKIDNEYMethodsMicroscopy, FluorescenceMOLECULAR BIOLOGYNEPHROLOGY

Identifiers

PMID39805676
PMCPMC12015034

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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.