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Haffner, J. J.

Publications and source records attributed to Haffner, J. J..

2 recordsLinked to original sources

Revealing Spatial Heterogeneity across the Gut Tissue-Lumen Interface through MALDI Mass Spectrometry Imaging

AbstractMetabolites play critical roles in modulating gut-microbe interactions and are closely related to health and disease consequences. One critical aspect of the gut-microbe interactions is spatial heterogeneity, particularly at the interface space between gut tissue and luminal contents, where a unique microhabitat of diverse microbial functions encounters the host tissues. Exploring the spatial heterogeneity of this interface enables insights into these gut-microbe interactions. Previous studies commonly investigated metabolome through tissue homogenization and bulk analysis, but these methods result in the loss of spatial information. In this project, we use high-resolution matrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI-MSI) approaches to reveal the chemical spatial heterogeneity of colon tissue, luminal contents, and the tissue-lumen interface across multiple colonic regions. We applied a swiping technique to aid the preservation of luminal content integrity and used two MALDI matrices to cover a wide range of metabolites. The MALDI-MSI analyses revealed distinct patterns of metabolite spatial localization across the gut tissue-lumen interfaces, amongst which the interface-enriched features are of particular interest due to their possibly connection to the gut-microbe interactions. Overall, the rich spatial heterogeneity of metabolomic profiles across the gut tissue-lumen interfaces highlight the molecular participants in host-microbe interactions, providing new opportunities for examining host-microbiome-metabolome dynamics.

biochemistry↗

Characterization of the workplace chemical exposome using untargeted LC-MS/MS: a case study

Western people now spend close to 90% of their time indoors, one-quarter of which occurs at their place of employment. As such, interactions between employees and the workplace built environment have significant potential impact on employee health and safety. However, the range of workers daily chemical exposures is still poorly understood. Likewise, the influence of workers themselves and of worker behavior on the chemical composition of the workplace is still unknown. In this case study, we used untargeted liquid chromatography-tandem mass spectrometry (LC-MS/MS) to compare the chemical signatures of three different types of workplaces: scientific research buildings, office buildings, and one mixed-purpose building. Our results identified differential signatures of public building surfaces based on building purpose, sampling location and surface materials. Overall, these results are helping define the influence of human behavior on the workplace chemical environment and identify the chemical hazards to which people are exposed throughout their workday. HighlightsO_LIImplementation of untargeted liquid chromatography-tandem mass spectrometry to study workplace chemical exposures. C_LIO_LIShared chemical signatures were identified based on building purpose. C_LIO_LIDifferential chemical signatures were identified based on surface material and sampling location. C_LIO_LIAnnotated molecules include pharmaceuticals, illicit drugs, food chemicals, constituents of paints and stains, and cleaning products. C_LI

biochemistry↗