Show simple item record

dc.contributor.advisorFan, Jing
dc.contributor.authorQing, Xin
dc.date.accessioned2024-11-22T23:59:42Z
dc.date.available2024-11-22T23:59:42Z
dc.date.issued2024-11-19
dc.identifier.urihttp://digital.library.wisc.edu/1793/89624
dc.description.abstractNeutrophils utilize a variety of metabolic sources to support their crucial functions as the first responders in innate immunity. Here, through in vivo and ex vivo isotopic tracing, we examined the contributions of different nutrients to neutrophil metabolism under specific conditions. Human peripheral blood neutrophils, in contrast to a neutrophil-like cell line, rely on glycogen storage as a major metabolic source under resting state but rapidly switch to primarily using extracellular glucose upon activation with various stimuli. This shift is driven by a substantial increase in glucose uptake, enabled by rapidly increased GLUT1 on cell membrane, that dominates the simultaneous increase in gross glycogen cycling capacity. Shifts in nutrient utilization impact neutrophil functions in a function-specific manner: oxidative burst depends on glucose utilization, whereas NETosis and phagocytosis can be flexibly supported by either glucose or glycogen, and neutrophil migration and fungal control are enhanced by the shift from glycogen utilization to glucose utilization. This work provides a quantitative and dynamic understanding of fundamental features in neutrophil metabolism and elucidates how metabolic remodeling shapes neutrophil functions, which has broad health relevance.en_US
dc.language.isoen_USen_US
dc.subjectNutrition and Metabolismen_US
dc.titleActivation induces shift in nutrient utilization that differentially impacts cell functions in human neutrophilsen_US
dc.typeThesisen_US
thesis.degree.disciplineNutrition and Metabolismen_US
thesis.degree.nameMSen_US
thesis.degree.grantorUniversity of Wisconsin-Madisonen_US


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record