Multimodal Imaging Mass Spectrometry to Identify Markers of Pulmonary Arterial Hypertension in Human Lung Tissue Using MALDI-ToF, ToF-SIMS, and Hybrid SIMS

  • Sebastiaan Van Nuffel
  • , Marceau Quatredeniers
  • , Alexander Pirkl
  • , Julia Zakel
  • , Jean Pierre Le Caer
  • , Nicolas Elie
  • , Quentin P. Vanbellingen
  • , Sébastien Joël Dumas
  • , Morad Kamel Nakhleh
  • , Maria Rosa Ghigna
  • , Elie Fadel
  • , Marc Humbert
  • , Pierre Chaurand
  • , David Touboul
  • , Sylvia Cohen-Kaminsky
  • , Alain Brunelle

Research output: Contribution to journalArticlepeer-review

Abstract

Pulmonary arterial hypertension (PAH) is a rare and deadly disease affecting roughly 15-60 people per million in Europe with a poorly understood pathology. There are currently no diagnostic tools for early detection nor does a curative treatment exist. The lipid composition of arteries in lung tissue samples from human PAH and control patients were investigated using matrix-assisted laser desorption ionization (MALDI) imaging mass spectrometry (IMS) combined with time-of-flight secondary ion mass spectrometry (TOF-SIMS) imaging. Using random forests as an IMS data analysis technique, it was possible to identify the ion at m/z 885.6 as a marker of PAH in human lung tissue. The m/z 885.6 ion intensity was shown to be significantly higher around diseased arteries and was confirmed to be a diacylglycerophosphoinositol PI(C18:0/C20:4) via MS/MS using a novel hybrid SIMS instrument. The discovery of a potential biomarker opens up new research avenues which may finally lead to a better understanding of the PAH pathology and highlights the vital role IMS can play in modern biomedical research.

Original languageEnglish
Pages (from-to)12079-12087
Number of pages9
JournalAnalytical Chemistry
Volume92
Issue number17
DOIs
Publication statusPublished - 1 Sept 2020
Externally publishedYes

Fingerprint

Dive into the research topics of 'Multimodal Imaging Mass Spectrometry to Identify Markers of Pulmonary Arterial Hypertension in Human Lung Tissue Using MALDI-ToF, ToF-SIMS, and Hybrid SIMS'. Together they form a unique fingerprint.

Cite this