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Fluorescence-mediated Tomography for the Detection and Quantification of Macrophage-related Murine Intestinal Inflammation
Published on: December 15, 2017
ROS Scavenging and inflammation-directed polydopamine nanoparticles regulate gut immunity and flora therapy in
Meiyu Bao1, Keyi Wang2, Jingqiang Li1
1Central Laboratory, Shanghai Tenth People's Hospital, School of Medicine, Tongji University, 301# Yanchang Middle Road, Shanghai, 200072, China.
Abstract:
Dysfunction of the intestinal mucosal immune system and dysbiosis of the intestinal microflora can induce inflammatory bowel disease. However, drug-mediated clinical treatment remains a challenge due to its poor therapeutic efficacy and severe side effects. Herein, a ROS scavenging and inflammation-directed nanomedicine is designed and fabricated by coupling polydopamine nanoparticles with mCRAMP, an antimicrobial peptide, while wrapping macrophage membrane in the outer layer. The designed nanomedicine reduced the secretion of pro-inflammatory cytokines and elevate the expression of anti-inflammatory cytokine in vivo and in vitro inflammation models, demonstrating its significant ability of improving inflammatory responses. Importantly, the macrophage membrane encapsulated nanoparticles exhibit the obviously enhanced targeting performance in local inflamed tissues. Furthermore, the 16S rRNA sequencing of fecal microorganisms showed that probiotics increased and pathogenic bacteria were inhibited after oral delivery the nanomedicine, indicating that the designed nano platform played a significant role in optimizing intestinal microbiome. Taken together, the designed nanomedicine are not only easy to prepare and exhibit high biocompatibility, but also show the inflammatory targeting property, anti-inflammatory function and positive regulation of intestinal flora, thus providing a new idea for the intervention and treatment of colitis. STATEMENT OF SIGNIFICANCE: Inflammatory bowel disease (IBD), a chronic and intractable disease, may lead to colon cancer in severe cases without effective treatment. However, clinical drugs are largely ineffective owing to insufficient therapeutic efficacies and side effects. Herein, we constructed a biomimetic polydopamine nanoparticle for oral administration to treat the IBD by modulating mucosal immune homeostasis and optimizing intestinal microorganisms. In vitro and in vivo experiments showed that the designed nanomedicine not only exhibits the anti-inflammatory function and inflammatory targeting property but also positively regulate the gut microflora. Taken together, the designed nanomedicine combined immunoregulation and intestinal microecology modulation to significantly enhance the therapeutic effect on colitis in mice, thus providing a new approach for the clinical treatment of colitis.
Insights
A novel nanomedicine effectively treats inflammatory bowel disease (IBD) by reducing inflammation and restoring gut bacteria balance. This biomimetic nanoparticle offers a promising, biocompatible approach for colitis intervention.
Area of Science:
- Biomaterials Science
- Immunology
- Microbiology
Background:
- Inflammatory bowel disease (IBD) arises from immune dysfunction and gut dysbiosis, posing treatment challenges due to limited drug efficacy and side effects.
- Current clinical treatments for IBD often suffer from poor therapeutic outcomes and significant adverse effects, necessitating novel therapeutic strategies.
Purpose of the Study:
- To design and fabricate a reactive oxygen species (ROS) scavenging and inflammation-directed nanomedicine for IBD treatment.
- To evaluate the nanomedicine's efficacy in modulating mucosal immunity, targeting inflamed tissues, and restoring intestinal microflora balance.
Main Methods:
- Fabrication of a nanomedicine by coupling polydopamine nanoparticles with mCRAMP peptide and encapsulating with macrophage membranes.
- In vitro and in vivo assessment of the nanomedicine's anti-inflammatory effects by measuring cytokine levels.
- Evaluation of the nanomedicine's targeting ability in inflamed tissues and its impact on gut microbiota composition using 16S rRNA sequencing.
Main Results:
- The nanomedicine effectively reduced pro-inflammatory cytokines and increased anti-inflammatory cytokines in inflammation models.
- Macrophage membrane encapsulation significantly enhanced the nanomedicine's targeting of inflamed intestinal tissues.
- Oral administration of the nanomedicine promoted probiotic growth and inhibited pathogenic bacteria, optimizing the intestinal microbiome.
Conclusions:
- The developed nanomedicine demonstrates potent anti-inflammatory properties and targeted delivery to inflamed sites, offering a new therapeutic avenue for colitis.
- This biomimetic nanoparticle approach successfully modulates mucosal immune homeostasis and intestinal microecology, significantly improving therapeutic effects for IBD.
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