Localized lipidomics in cystic fibrosis: TOF-SIMS imaging of lungs from Pseudomonas aeruginosa-infected mice

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• 作者：Nicolas Desbenoit^a ; Emilie Saussereau^b ; ^c ; Claudia Bich^a ; Matthieu Bourderioux^b ; ^c ; Janine Fritsch^b ; ^c ; Aleksander Edelman^b ; ^c ; Alain Brunelle^a ; Mario Ollero^a ; ^b ; ^c ; ¹ ; ² ; ^{Mario.ollero@inserm.fr" class="auth_mail}
• 关键词：Mass spectrometry ; TOF-SIMS ; Phosphoinositol ; Cholesteryl sulfate ; Bronchial epithelium
• 刊名：The International Journal of Biochemistry and Cell Biology
• 出版年：July 2014
• 年：2014
• 卷：52
• 期：Complete
• 页码：77-82
• 全文大小：1746 K

文摘

A consistent body of research has linked cystic fibrosis (CF) with variations in the tissue and fluid content in a number of lipid molecules. However, little is known about the spatial localization of those variations. We have recently applied TOF-SIMS mass spectrometry imaging to detect differential lipid signatures at the colon epithelium between normal and cftr−/− mice. In the present work we have used this technology to investigate potential differences in the spatial distribution of lipids due to Pseudomonas aeruginosa (P.a.) infection in mouse lung expressing or not cftr. Wild-type and exon 10 cftr knockout mice were subjected to intranasal infection with a clinical strain of P.a. Lung cryosections from infected and non-infected mice were subjected to cluster TOF-SIMS analysis in the negative ion mode. We observed a highly specific localization of a phosphoinositol fragment ion at m/z 299.1 in bronchial epithelium. Using this ion to delineate a region of interest, we studied the relative abundance of ions below m/z 1500. We found a significant increase in m/z 465.4 (identified as cholesteryl sulfate) in cftr−/− epithelium and in response to bacterial infection, as well as a decrease in most carboxylic ions. In conclusion, the m/z 299.1 ion can be used as a marker of bronchial epithelium, where P.a. infection leads to increased presence of cholesteryl sulfate in this tissue. TOF-SIMS imaging reveals as a valuable tool for the study of respiratory epithelium.

This article is part of a Directed Issue entitled: Cystic Fibrosis: From o-mics to cell biology, physiology, and therapeutic advances.