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Glycolytic activation of CD14+ intestinal macrophages contributes to the inflammatory responses via exosomal membrane tumor necrosis factor in Crohn’s disease

Macrophage (Mφ) activation plays a critical role in the inflammatory response. Activated Mφ go through profound reprogramming of cellular metabolism. However, changes in their intracellular energy metabolism and its effect on inflammatory responses in Crohn’s disease (CD) remain currently unclear. T...

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Hauptverfasser: Zeng, Ziwei (VerfasserIn) , Cheng, Sijing (VerfasserIn) , Li, Xuanna (VerfasserIn) , Liu, Huashan (VerfasserIn) , Lin, Jinxin (VerfasserIn) , Liang, Zhenxing (VerfasserIn) , Liu, Xuanhui (VerfasserIn) , Cao, Chao (VerfasserIn) , Li, Shujuan (VerfasserIn) , He, Xiaowen (VerfasserIn) , Kang, Liang (VerfasserIn) , Wu, Xiaojian (VerfasserIn) , Zheng, Xiaobin (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: January 2024
In: Inflammatory bowel diseases
Year: 2024, Jahrgang: 30, Heft: 1, Pages: 90-102
ISSN:1536-4844
DOI:10.1093/ibd/izad117
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1093/ibd/izad117
Verlag, lizenzpflichtig, Volltext: https://academic.oup.com/ibdjournal/article/30/1/90/7219968
Volltext
Verfasserangaben:Ziwei Zeng, MD, PhD, Sijing Cheng, MD, PhD Xuanna Li, MD, PhD, Huashan Liu, MD, PhD, Jinxin Lin, MD, PhD, Zhenxing Liang, MD, PhD, Xuanhui Liu, MD, PhD, Chao Cao, MD, PhD, Shujuan Li, MD, PhD, Xiaowen He, MD, PhD, Liang Kang, MD, PhD, Xiaojian Wu, MD, PhD, and Xiaobin Zheng, MD, PhD
Beschreibung
Zusammenfassung:Macrophage (Mφ) activation plays a critical role in the inflammatory response. Activated Mφ go through profound reprogramming of cellular metabolism. However, changes in their intracellular energy metabolism and its effect on inflammatory responses in Crohn’s disease (CD) remain currently unclear. The aim of this study is to explore metabolic signatures of CD14+ Mφ and their potential role in CD pathogenesis as well as the underlying mechanisms.CD14+ Mφ were isolated from peripheral blood or intestinal tissues of CD patients and control subjects. Real-time flux measurements and enzyme-linked immunosorbent assay were used to determine the inflammatory states of Mφ and metabolic signatures. Multiple metabolic routes were suppressed to determine their relevance to cytokine production.Intestinal CD14+ Mφ in CD patients exhibited activated glycolysis compared with those in control patients. Specifically, macrophagic glycolysis in CD largely induced inflammatory cytokine release. The intestinal inflammatory microenvironment in CD elicited abnormal glycolysis in Mφ. Mechanistically, CD14+ Mφ derived exosomes expressed membrane tumor necrosis factor (TNF), which engaged TNFR2 and triggered glycolytic activation via TNF/nuclear factor κB autocrine and paracrine signaling. Importantly, clinically applicable anti-TNF antibodies effectively prevented exosomal membrane TNF-induced glycolytic activation in CD14+ Mφ.CD14+ Mφ take part in CD pathogenesis by inducing glycolytic activation via membrane TNF-mediated exosomal autocrine and paracrine signaling. These results provide novel insights into pathogenesis of CD and enhance understanding of the mechanisms of anti-TNF agents.
Beschreibung:Im Titel ist das Plus-Zeichen hochgestellt
Online veröffentlicht: 5. Juli 2023
Gesehen am 22.02.2024
Beschreibung:Online Resource
ISSN:1536-4844
DOI:10.1093/ibd/izad117

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