Assessment of inflammatory suppression and fibroblast infiltration in tissue remodelling by supercritical CO acellular dermal matrix (scADM) utilizing Sprague Dawley models.
Abstract
Human skin-derived ECM aids cell functions but can trigger immune reactions; therefore it is addressed through decellularization. Acellular dermal matrices (ADMs), known for their regenerative properties, are used in tissue and organ regeneration. ADMs now play a key role in plastic and reconstructive surgery, enhancing aesthetics and reducing capsular contracture risk. Innovative decellularization with supercritical carbon dioxide preserves ECM quality for clinical use. The study investigated the cytotoxicity, biocompatibility, and anti-inflammatory properties of supercritical CO acellular dermal matrix (scADM) based on Sprague Dawley rat models. Initial experiments with fibroblast cells confirmed the non-toxic nature of scADM and demonstrated cell infiltration into scADMs after incubation. Subsequent tests revealed the ability of scADM to suppress inflammation induced by lipopolysaccharides (LPS) presenting by the reduction of pro-inflammatory cytokines TNF-α, IL-6, IL-1β, and MCP-1. In the model, histological assessment of implanted scADMs in 6 months revealed a decrease in inflammatory cells, confirmed further by the biomarkers of inflammation in immunofluorescence staining. Besides, an increase in fibroblast infiltration and collagen formation was observed in histological staining, which was supported by various biomarkers of fibroblasts. Moreover, the study demonstrated vascularization and macrophage polarization, depicting increased endothelial cell formation. Alteration of matrix metalloproteinases (MMPs) was analyzed by RT-PCR, indicating the reduction of MMP2, MMP3, and MMP9 levels over time. Simultaneously, an increase in collagen deposition of collagen I and collagen III was observed, verified in immunofluorescent staining, RT-PCR, and western blotting. Overall, the findings suggested that scADMs offer significant benefits in improving outcomes in implant-based procedures as well as soft tissue substitution.
추출된 의학 개체 (NER)
| 유형 | 영어 표현 | 한국어 / 풀이 | UMLS CUI | 출처 | 등장 |
|---|---|---|---|---|---|
| 재료 | acellular dermal matrix
|
무세포진피기질 | dict | 2 | |
| 해부 | fibroblast
|
scispacy | 1 | ||
| 해부 | tissue
|
scispacy | 1 | ||
| 해부 | organ
|
scispacy | 1 | ||
| 해부 | ECM
|
scispacy | 1 | ||
| 해부 | fibroblast cells
|
scispacy | 1 | ||
| 해부 | cell
|
scispacy | 1 | ||
| 해부 | fibroblasts
|
scispacy | 1 | ||
| 해부 | macrophage
|
scispacy | 1 | ||
| 해부 | endothelial cell
|
scispacy | 1 | ||
| 해부 | soft tissue
|
scispacy | 1 | ||
| 합병증 | Acellular dermal
|
scispacy | 1 | ||
| 합병증 | capsular contracture
|
피막구축 | dict | 1 | |
| 약물 | carbon dioxide
|
C0007012
carbon dioxide
|
scispacy | 1 | |
| 약물 | lipopolysaccharides
|
C0023810
Lipopolysaccharides
|
scispacy | 1 | |
| 약물 | LPS
→ lipopolysaccharides
|
C0023810
Lipopolysaccharides
|
scispacy | 1 | |
| 질환 | contracture
|
C0009917
Contracture
|
scispacy | 1 | |
| 질환 | inflammation
|
C0021368
Inflammation
|
scispacy | 1 | |
| 질환 | ADMs
→ Acellular dermal matrices
|
scispacy | 1 | ||
| 기타 | CO acellular dermal matrix
|
scispacy | 1 | ||
| 기타 | Sprague Dawley
|
scispacy | 1 | ||
| 기타 | Human skin-derived ECM aids cell
|
scispacy | 1 | ||
| 기타 | Sprague Dawley rat
|
scispacy | 1 | ||
| 기타 | IL-6
|
scispacy | 1 | ||
| 기타 | MCP-1
|
scispacy | 1 | ||
| 기타 | collagen
|
scispacy | 1 | ||
| 기타 | matrix metalloproteinases
|
scispacy | 1 | ||
| 기타 | MMPs
→ matrix metalloproteinases
|
scispacy | 1 | ||
| 기타 | MMP2
|
scispacy | 1 | ||
| 기타 | MMP3
|
scispacy | 1 | ||
| 기타 | MMP9
|
scispacy | 1 |
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