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DESI-MSI-guided exploration of metabolic-phenotypic relationships reveals a correlation between PI 38:3 and proliferating cells in clear cell renal cell carcinoma via single-section co-registration of multimodal imaging

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  • معلومة اضافية
    • Contributors:
      Innovate UK; University of St Andrews.School of Medicine; University of St Andrews.Cellular Medicine Division; University of St Andrews.Sir James Mackenzie Institute for Early Diagnosis
    • الموضوع:
      2024
    • Collection:
      University of St Andrews: Digital Research Repository
    • نبذة مختصرة :
      Funding: NuCana PLC, The Melville Trust, Innovate UK (104690), Horizon Europe (10107453). ; A workflow has been evaluated that utilizes a single tissue section to obtain spatially co-registered, molecular, and phenotypical information suitable for AI-enabled image analysis. Desorption electrospray ionization mass spectrometry imaging (DESI-MSI) was used to obtain molecular information followed by conventional histological staining and immunolabelling. The impact of varying DESI-MSI conditions (e.g., heated transfer line (HTL) temperature, scan rate, acquisition time) on the detection of small molecules and lipids as well as on tissue integrity crucial for integration into typical clinical pathology workflows was assessed in human kidney. Increasing the heated transfer line temperature from 150 to 450 °C resulted in a 1.8-fold enhancement in lipid signal at a scan rate of 10 scans/s, while preserving histological features. Moreover, increasing the acquisition speed to 30 scans/s yielded superior lipid signal when compared to 10 scans/s at 150 °C. Tissue morphology and protein epitopes remained intact allowing full histological assessment and further multiplex phenotyping by immunofluorescence (mIF) and immunohistochemistry (mIHC) of the same section. The successful integration of the workflow incorporating DESI-MSI, H&E, and immunolabelling on a single tissue section revealed an accumulation of ascorbic acid in regions of focal chronic inflammatory cell infiltrate within non-cancerous kidney tissue. Additionally, a strong positive correlation between PI 38:3 and proliferating cells was observed in clear cell renal cell carcinoma (ccRCC) showing the utility of this approach in uncovering molecular associations in disease pathology. ; Peer reviewed
    • File Description:
      application/pdf
    • Relation:
      Analytical and Bioanalytical Chemistry; 302270036; 85194422409; https://hdl.handle.net/10023/30032; https://www.scopus.com/pages/publications/85194422409; TS/S013121/1
    • الرقم المعرف:
      10.1007/s00216-024-05339-0
    • الدخول الالكتروني :
      https://hdl.handle.net/10023/30032
      https://doi.org/10.1007/s00216-024-05339-0
      https://www.scopus.com/pages/publications/85194422409
    • Rights:
      Copyright © The Author(s) 2024. This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
    • الرقم المعرف:
      edsbas.EE62AEFE