In situ molecular profiles of glomerular cells by integrated imaging mass spectrometry and multiplexed immunofluorescence microscopy

Allison B. Esselman, Felipe A. Moser, Léonore E.M. Tideman, Lukasz G. Migas, Katerina V. Djambazova, Madeline E. Colley, Ellie L. Pingry, Nathan Heath Patterson, Melissa A. Farrow, Haichun Yang, Agnes B. Fogo, Mark de Caestecker, Raf Van de Plas*, Jeffrey M. Spraggins*

*Corresponding author for this work

Research output: Contribution to journalArticleScientificpeer-review

Abstract

Glomeruli filter blood through the coordination of podocytes, mesangial cells, fenestrated endothelial cells, and the glomerular basement membrane. Cellular changes, such as podocyte loss, are associated with pathologies like diabetic kidney disease. However, little is known regarding the in situ molecular profiles of specific cell types and how these profiles change with disease. Matrix-assisted laser desorption/ionization imaging mass spectrometry (MALDI IMS) is well-suited for untargeted tissue mapping of a wide range of molecular classes. Importantly, additional imaging modalities can be integrated with MALDI IMS to associate these biomolecular distributions to specific cell types. Here, we integrated workflow combining MALDI IMS and multiplexed immunofluorescence (MxIF) microscopy. High spatial resolution MALDI IMS (5 μm) was used to determine lipid distributions within human glomeruli from a normal portion of fresh-frozen kidney cancer nephrectomy tissue revealing intra-glomerular lipid heterogeneity. Mass spectrometric data were linked to specific glomerular cell types and substructures through new methods that enable MxIF microscopy to be performed on the same tissue section following MALDI IMS, without sacrificing signal quality from either modality. Machine learning approaches were combined enabling cell type segmentation and identification based on MxIF data. This was followed by mining of cell type or cluster-associated MALDI IMS signatures using classification and interpretable machine learning. This allowed automated discovery of spatially specific molecular markers for glomerular cell types and substructures as well as lipids correlated to deep and superficial glomeruli. Overall, our work establishes a toolbox for probing molecular signatures of glomerular cell types and substructures within tissue microenvironments providing a framework applicable to other kidney tissue features and organ systems.

Original languageEnglish
Pages (from-to)332-337
Number of pages6
JournalKidney International
Volume107
Issue number2
DOIs
Publication statusPublished - 2025

Keywords

  • cellular analysis
  • glomeruli
  • immunofluorescence
  • lipidomics
  • MALDI IMS
  • multimodal imaging

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