ArticleJournal of nanobiotechnology2025
Cell-laden biomimetic microneedles reconstruct skin rete ridge and stem cell niche.
Article in Journal of nanobiotechnology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
3 citing papers in PubMed.
- Glucose-responsive "sense-and-treat" microneedle patch for promoting diabetic chronic wound healing.Materials today. Bio · 2026Article
- Advances in 3D Printed Microneedles as a Prototype for Skin Targeted Therapeutics in Personalized Dermal Pharmaceuticals.AAPS PharmSciTech · 2025Review
- A side-effect-free chemotactic-antibacterial wound dressing for programmatic trapping, killing of bacteria, and wound repair.Materials today. Bio · 2025Article
Corrections and comments
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Authors and funding
10 authors.
Funding
Abstract
The traditional skin graft wound repair strategy for burns is unable to reconstruct the normal anatomy of the skin, resulting in quality problems such as scarring, which have always been the bottleneck of burn medicine. The skin rete ridge (RRs) is an important basis for maintaining skin homeostasis, but the complete reconstruction of the RRs in wound repair is still difficult with traditional split-thickness skin grafting and wound cell therapy. In this study, based on our previous experience of wound epidermal stem cell (EpiSCs) therapy, we further designed and optimized the bionic RRs microneedles loaded with human EpiSCs (C-Ms). Transplanting C-Ms into full-thickness wounds in nude mice promotes the formation of RRs similar to natural human epidermis and provides stem cell niches. Pathway enrichment analysis showed that C-Ms transplantation into wounds reshapes the extracellular matrix (ECM) and reduces wound healing fibrosis through FAK, ECM receptor interaction signaling pathways. Moreover, C-Ms improve wound healing by accelerating early vascularization, and they also regulate the proliferation of EpiSCs to further promote the formation of RRs structure. These results suggest that C-Ms can compensate for the lack of skin anatomical structure, which may be suitable for use in clinical patients with large-scale burns.
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Registered trials
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