# Large Fibrous Connective Tissue Reduces Oxidative Stress to Form a Living Cell Scaffold in Adipose Grafts

**Authors:** Qiang Yue, Zilong Cao, Tiran Zhang, Ningbei Yin, Liqiang Liu

PMC · DOI: 10.3390/antiox14030270 · Antioxidants · 2025-02-26

## TL;DR

Large fibrous connective tissue improves fat graft survival by reducing oxidative stress and forming a supportive cell scaffold.

## Contribution

The study reveals a novel mechanism where LFC tissue enhances fat graft survival through antioxidant activity and structural support.

## Key findings

- Intact fat with LFC shows significantly higher survival rates compared to liposuctioned fat.
- LFC promotes SOD1 expression, enhances respiratory chain RNA, and reduces ROS and inflammation.
- LFC forms a mesh-like structure that supports viable fat cells and improves long-term graft survival.

## Abstract

This study aimed to investigate the mechanisms by which large fibrous connective (LFC) tissue enhances fat graft survival in fat transplantation. A block fat graft model demonstrated that intact fat containing LFC showed significantly higher survival rates compared with liposuctioned fat. In the center of intact grafts, viable fat cells surrounded the LFC, forming a mesh-like living tissue structure. Proteomics of the extracellular matrix (ECM) adjacent to LFC (ALFC) and distant to LFC (DLFC) revealed significant differences in mitochondrial aspects. Staining of LFC tissue showed that it contains a large number of blood vessels and mitochondria, and exhibits stronger antioxidant capacity (p < 0.05) compared with adipose tissue. By mixing LFC with liposuctioned fat and transplanting into nude mice, histological sections showed that LFC promotes SOD1 expression, enhances respiratory chain RNA expression, and reduces ROS and inflammation. Pure mitochondrial-assisted fat transplantation only reduced short-term graft inflammation without improving long-term survival rates. In conclusion, LFC enhances long-term survival rates by reducing oxidative stress in fat grafts and forming a center for fat cell survival, thereby overcoming distance limitations. This represents a novel mechanism distinct from classical fat survival models and provides a reference for clinical practice.

## Linked entities

- **Genes:** SOD1 (superoxide dismutase 1) [NCBI Gene 6647]

## Full-text entities

- **Genes:** Sod1 (superoxide dismutase 1, soluble) [NCBI Gene 20655] {aka B430204E11Rik, Cu/Zn-SOD, CuZnSOD, Ipo-1, Ipo1, SODC}
- **Diseases:** inflammation (MESH:D007249)
- **Chemicals:** ROS (-)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11939587/full.md

## References

70 references — full list in the complete paper: https://tomesphere.com/paper/PMC11939587/full.md

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Source: https://tomesphere.com/paper/PMC11939587