Luminol-conjugated cyclodextrin biological nanoparticles for the treatment of severe burn-induced intestinal barrier disruption
- Burns & Trauma Vol. 12, Issue 1, (2024)
- 作者机构：
1. Department of Urology
2. The Army Medical University
3. Department of Urology, The First Affiliated Hospital of Chongqing Medical University
4. Institute of Burn Research, Southwest Hospital
5. Department of Urology, Chongqing University Three Gorges Hospital
6. Department of Rehabilitation
- 作者简介：
- 基金信息：
DOI：10.1093/burnst/tkad054
CLC：Published：2024，
Published Online：13 March 2024，
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Yajun Song, Yang Li, Wengang Hu, Feng Li, Hao Sheng, Chibing Huang, Xin Gou, Jingming Hou, Ji Zheng, Ya Xiao, Luminol-conjugated cyclodextrin biological nanoparticles for the treatment of severe burn-induced intestinal barrier disruption, Burns & Trauma, Volume 12, 2024, tkad054, https://doi.org/10.1093/burnst/tkad054
Yajun Song, Yang Li, Wengang Hu, Feng Li, Hao Sheng, Chibing Huang, Xin Gou, Jingming Hou, Ji Zheng, Ya Xiao, Luminol-conjugated cyclodextrin biological nanoparticles for the treatment of severe burn-induced intestinal barrier disruption, Burns & Trauma, Volume 12, 2024, tkad054, https://doi.org/10.1093/burnst/tkad054 DOI：
摘要
Abstract
BackgroundThe breakdown of intestinal barrier integrity occurs after severe burn injury and is responsible for the subsequent reactions of inflammation and oxidative stress. A new protective strategy for the intestinal barrier is urgently needed due to the limitations of the traditional methods. Recently
the application of nanoparticles has become one of the promising therapies for many inflammation-related diseases or oxidative damage. Herein
we developed a new anti-inflammatory and antioxidant nanoparticle named luminol-conjugated cyclodextrin (LCD) and aimed to evaluate its protective effects in severe burn-induced intestinal injury.MethodsFirst
LCD nanoparticles
engineered with covalent conjugation between luminol and β-cyclodextrin (β-CD)
were synthesized and examined. Then a mouse burn model was successfully established before the mouse body weight
intestinal histopathological manifestation
permeability
tight junction (TJ) expression and pro-inflammatory cytokines were determined in different groups. The proliferation
apoptosis
migration and reactive oxygen species (ROS) of intestinal epithelial cells (IECs) were assessed. Intraepithelial lymphocytes (IELs) were isolated and cultured for analysis by flow cytometry.ResultsLCD nanoparticle treatment significantly relieved the symptoms of burn-induced intestinal injury in the mouse model
including body weight loss and intestinal permeability abnormalities. Moreover
LCD nanoparticles remarkably recovered the mechanical barrier of the intestine after severe burn
renewed TJ structures
promoted IEC proliferation and migration
and inhibited IEC apoptosis. Mechanistically
LCD nanoparticles dramatically alleviated pro-inflammation factors (tumor necrosis factor-α
IL-17A) and ROS accumulation
which could be highly involved in intestinal barrier disruption. Furthermore
an increase in IL-17A and the proportion of IL-17A+Vγ4+ γδ T subtype cells was also observed in vitro in LPS-treated Vγ4+ γδ T cells
but the use of LCD nanoparticles suppressed this increase.ConclusionsTaken together
these findings demonstrate that LCD nanoparticles have the protective ability to ameliorate intestinal barrier disruption and provide a therapeutic intervention for burn-induced intestinal injury.
关键词
Keywords
LCD nanoparticleBurnIntestinal barrierInflammatory cytokinesReactive oxygen speciesVγ4+ γδ T cellsLuminol-conjugated cyclodextrin
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