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Engineered Probiotic-Silver Nanointerfaces Enable Multimodal Repair of Inflamed Colon via Wnt and Chemokine
Muhammad Farhan Rahim1, Saisai Gong1, Shah Nawaz2
1College of Veterinary Medicine, Huazhong Agricultural University, Wuhan 430070; P.R. China.
A novel nano-silver composite, stabilized by tannic acid-iron and derived from Bacillus licheniformis, effectively treats experimental colitis. This biohybrid therapy restores gut health and reduces systemic inflammation by remodeling epithelial repair and immune signaling pathways.
Area of Science:
- Biomaterials Science
- Nanomedicine
- Gastroenterology
Background:
- Inflammatory bowel disease (IBD) pathogenesis involves complex failures in epithelial integrity, immune cell migration, and inflammatory homeostasis.
- Multifunctional therapeutic strategies are crucial for addressing the multifaceted nature of IBD.
- Developing advanced nanotherapeutic platforms offers a promising avenue for IBD treatment.
Purpose of the Study:
- To develop and evaluate a Bacillus licheniformis-templated nano-silver (Nano-Ag) composite within a tannic acid-iron (TA-Fe) metal-phenolic network for treating TNBS-induced colitis.
- To assess the physicochemical properties and therapeutic efficacy of the engineered biohybrid nanotherapeutic platform.
- To elucidate the molecular mechanisms underlying the therapeutic effects of the Nano-Ag composite.
Main Methods:
- Fabrication of a TA-Fe metal-phenolic network encapsulating Bacillus licheniformis-templated Nano-Ag.
- In vivo administration of the Nano-Ag composite in a TNBS-induced colitis mouse model.
- Assessment of therapeutic effects through clinical observations, histological analysis, molecular marker evaluation, and serum profiling.
Main Results:
- The Nano-Ag composite demonstrated favorable physicochemical properties and a dose-responsive protective effect in vivo.
- Treatment significantly improved survival, reduced disease activity, preserved colon length, and restored colonic histoarchitecture.
- Molecular analysis revealed suppression of LEF-1, restoration of axin, attenuation of CXCR2/CCR7, and recovery of CCR5, indicating normalized Wnt signaling and immune trafficking.
- Serum profiling showed broad modulation of chemokine networks and partial correction of gut-liver and gut-kidney axis dysfunction.
Conclusions:
- The engineered TA-Fe-stabilized probiotic Nano-Ag platform acts as a multifunctional therapeutic agent for experimental colitis.
- The therapy integrates epithelial repair, inflammatory signaling modulation, and systemic metabolic stress reduction.
- This biohybrid nanomedicine represents a promising strategy for developing next-generation treatments for inflammatory bowel disease.
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